Skip to main content
Erschienen in: Cancer Chemotherapy and Pharmacology 4/2016

26.12.2015 | Review Article

Epigenetic alternations and cancer chemotherapy response

verfasst von: Jin-Feng Lv, Lei Hu, Wei Zhuo, Cong-Min Zhang, Hong-Hao Zhou, Lan Fan

Erschienen in: Cancer Chemotherapy and Pharmacology | Ausgabe 4/2016

Einloggen, um Zugang zu erhalten

Abstract

Epigenetics, referring to alterations in gene expression without a change in nucleotide sequence in eukaryotes, mainly includes DNA methylation, miRNA and histone modification. In recent years, accumulating evidences have shown that epigenetic aberrations not only play important roles in the initiation and development of human cancers but also affect cancer chemotherapy response by altering the expression of key genes involved in the absorption, distribution, metabolism and excretion of drugs or those correlated with progression or severity of cancers. These epigenetic alterations, along with advanced detecting techniques, have great potential to be used as predictive and prognostic biomarkers for personalized therapy, especially in the field of cancer treatment. Here we provide an overview of recent findings on epigenetic alterations involved in cancer chemotherapy response, with the aim of promoting rational use of chemotherapy drugs in the clinic.
Literatur
1.
Zurück zum Zitat Verma M (2013) Cancer control and prevention: nutrition and epigenetics. Curr Opin Clin Nutr Metab Care 16:376–384PubMedCrossRef Verma M (2013) Cancer control and prevention: nutrition and epigenetics. Curr Opin Clin Nutr Metab Care 16:376–384PubMedCrossRef
2.
Zurück zum Zitat Hojjat-Farsangi M (2015) Novel and emerging targeted-based cancer therapy agents and methods. Tumor Biol 36:543–556CrossRef Hojjat-Farsangi M (2015) Novel and emerging targeted-based cancer therapy agents and methods. Tumor Biol 36:543–556CrossRef
3.
Zurück zum Zitat Evans WE, Johnson JA (2001) Pharmacogenomics: the inherited basis for interindividual differences in drug response. Annu Rev Genomics Hum Genet 2:9–39PubMedCrossRef Evans WE, Johnson JA (2001) Pharmacogenomics: the inherited basis for interindividual differences in drug response. Annu Rev Genomics Hum Genet 2:9–39PubMedCrossRef
4.
Zurück zum Zitat Henikoff S, Matzke MA (1997) Exploring and explaining epigenetic effects. Trends Genet 13:293–295PubMedCrossRef Henikoff S, Matzke MA (1997) Exploring and explaining epigenetic effects. Trends Genet 13:293–295PubMedCrossRef
5.
Zurück zum Zitat Liu MZ, McLeod HL, He FZ, Chen XP, Zhou HH, Shu Y (2014) Epigenetic perspectives on cancer chemotherapy response. Pharmacogenomics 15:699–715PubMedCrossRef Liu MZ, McLeod HL, He FZ, Chen XP, Zhou HH, Shu Y (2014) Epigenetic perspectives on cancer chemotherapy response. Pharmacogenomics 15:699–715PubMedCrossRef
7.
Zurück zum Zitat Nana-Sinkam SP, Croce CM (2006) MicroRNAs in cell proliferation, cell death, and tumorigenesis. Br J Cancer 94:776–780CrossRef Nana-Sinkam SP, Croce CM (2006) MicroRNAs in cell proliferation, cell death, and tumorigenesis. Br J Cancer 94:776–780CrossRef
8.
Zurück zum Zitat Ivanov M, Kacevska M, Ingelman-Sundberg M (2012) Epigenomics and interindividual differences in drug response. Clin Pharmacol Ther 92:727–736PubMedCrossRef Ivanov M, Kacevska M, Ingelman-Sundberg M (2012) Epigenomics and interindividual differences in drug response. Clin Pharmacol Ther 92:727–736PubMedCrossRef
9.
10.
Zurück zum Zitat Tang J, Xiong Y, Zhou HH, Chen XP (2014) DNA methylation and personalized medicine. J Clin Pharm Ther 39:621–627PubMedCrossRef Tang J, Xiong Y, Zhou HH, Chen XP (2014) DNA methylation and personalized medicine. J Clin Pharm Ther 39:621–627PubMedCrossRef
11.
Zurück zum Zitat Iwai N, Naraba H (2005) Polymorphisms in human pre-miRNAs. Biochem Biophys Res Commun 331:1439–1444PubMedCrossRef Iwai N, Naraba H (2005) Polymorphisms in human pre-miRNAs. Biochem Biophys Res Commun 331:1439–1444PubMedCrossRef
12.
13.
Zurück zum Zitat Irizarry RA, Ladd-Acosta C, Wen B, Wu Z, Montano C, Onyango P (2009) The human colon cancer methylome shows similar hypo-and hypermethylation at conserved tissue-specific CpG island shores. Nat Genet 41:178–186PubMedPubMedCentralCrossRef Irizarry RA, Ladd-Acosta C, Wen B, Wu Z, Montano C, Onyango P (2009) The human colon cancer methylome shows similar hypo-and hypermethylation at conserved tissue-specific CpG island shores. Nat Genet 41:178–186PubMedPubMedCentralCrossRef
14.
Zurück zum Zitat Chekhun VF, Kulik GI, Yurchenko OV (2006) Role of DNA hypomethylation in the development of the resistance to doxorubicin in human MCF-7 breast adenocarcinoma cells. Cancer Lett 231:87–93PubMedCrossRef Chekhun VF, Kulik GI, Yurchenko OV (2006) Role of DNA hypomethylation in the development of the resistance to doxorubicin in human MCF-7 breast adenocarcinoma cells. Cancer Lett 231:87–93PubMedCrossRef
15.
Zurück zum Zitat Dejeux E, Rønneberg JA, Solvang H, Bukholm I, Geisler S, Aas T (2010) Research DNA methylation profiling in doxorubicin treated primary locally advanced breast tumours identifies novel genes associated with survival and treatment response. Mol Cancer 9:68PubMedPubMedCentralCrossRef Dejeux E, Rønneberg JA, Solvang H, Bukholm I, Geisler S, Aas T (2010) Research DNA methylation profiling in doxorubicin treated primary locally advanced breast tumours identifies novel genes associated with survival and treatment response. Mol Cancer 9:68PubMedPubMedCentralCrossRef
16.
Zurück zum Zitat Tsang WP, Kwok TT (2007) Riboregulator H19 induction of MDR1-associated drug resistance in human hepatocellular carcinoma cells. Oncogene 26:4877–4881PubMedCrossRef Tsang WP, Kwok TT (2007) Riboregulator H19 induction of MDR1-associated drug resistance in human hepatocellular carcinoma cells. Oncogene 26:4877–4881PubMedCrossRef
17.
Zurück zum Zitat Turner JG, Gump JL, Zhang C, Cook JM, Marchion D, Hazlehurst L (2006) ABCG2 expression, function, and promoter methylation in human multiple myeloma. Blood 108:3881–3889PubMedPubMedCentralCrossRef Turner JG, Gump JL, Zhang C, Cook JM, Marchion D, Hazlehurst L (2006) ABCG2 expression, function, and promoter methylation in human multiple myeloma. Blood 108:3881–3889PubMedPubMedCentralCrossRef
18.
Zurück zum Zitat Litman T, Brangi M, Hudson E, Fetsch P, Abati A, Ross DD (2000) The multidrug-resistant phenotype associated with overexpression of the new ABC half-transporter, MXR (ABCG2). J Cell Sci 113:2011–2021PubMed Litman T, Brangi M, Hudson E, Fetsch P, Abati A, Ross DD (2000) The multidrug-resistant phenotype associated with overexpression of the new ABC half-transporter, MXR (ABCG2). J Cell Sci 113:2011–2021PubMed
19.
Zurück zum Zitat Gagnon JF, Bernard O, Villeneuve L, Têtu B, Guillemette C (2006) Irinotecan inactivation is modulated by epigenetic silencing of UGT1A1 in Colon Cancer. Clin Cancer Res 12:1850–1858PubMedCrossRef Gagnon JF, Bernard O, Villeneuve L, Têtu B, Guillemette C (2006) Irinotecan inactivation is modulated by epigenetic silencing of UGT1A1 in Colon Cancer. Clin Cancer Res 12:1850–1858PubMedCrossRef
20.
Zurück zum Zitat Kim SJ, Kang HS, Jung SY, Min SY, Lee S, Kim SW (2010) Methylation patterns of genes coding for drug-metabolizing enzymes in tamoxifen-resistant breast cancer tissues. J Mol Med 88:1123–1131PubMedCrossRef Kim SJ, Kang HS, Jung SY, Min SY, Lee S, Kim SW (2010) Methylation patterns of genes coding for drug-metabolizing enzymes in tamoxifen-resistant breast cancer tissues. J Mol Med 88:1123–1131PubMedCrossRef
21.
Zurück zum Zitat Nakamichi I, Tomita Y, Zhang B, Sugiyama H, Kanakura Y, Fukuhara S (2007) Correlation between promoter hypermethylation of GSTP1 and response to chemotherapy in diffuse large B cell lymphoma. Ann Hematol 86:557–564PubMedCrossRef Nakamichi I, Tomita Y, Zhang B, Sugiyama H, Kanakura Y, Fukuhara S (2007) Correlation between promoter hypermethylation of GSTP1 and response to chemotherapy in diffuse large B cell lymphoma. Ann Hematol 86:557–564PubMedCrossRef
22.
Zurück zum Zitat Sieuwerts AM, Lyng MB, Meijer-van Gelder ME, de Weerd V, Sweep FC, Foekens JA (2014) Evaluation of the ability of adjuvant tamoxifen-benefit gene signatures to predict outcome of hormone-naive estrogen receptor- positive breast cancer patients treated with tamoxifen in the advanced setting. Mol Oncol 8:1679–1689PubMedCrossRef Sieuwerts AM, Lyng MB, Meijer-van Gelder ME, de Weerd V, Sweep FC, Foekens JA (2014) Evaluation of the ability of adjuvant tamoxifen-benefit gene signatures to predict outcome of hormone-naive estrogen receptor- positive breast cancer patients treated with tamoxifen in the advanced setting. Mol Oncol 8:1679–1689PubMedCrossRef
23.
Zurück zum Zitat Chen Y, Tang Y, Guo C (2012) Nuclear receptors in the multidrug resistance through the regulation of drug-metabolizing enzymes and drug transporters. Biochem Pharmacol 83:1112–1126PubMedPubMedCentralCrossRef Chen Y, Tang Y, Guo C (2012) Nuclear receptors in the multidrug resistance through the regulation of drug-metabolizing enzymes and drug transporters. Biochem Pharmacol 83:1112–1126PubMedPubMedCentralCrossRef
24.
Zurück zum Zitat Raynal C, Pascussi JM, Leguelinel G (2010) Pregnane X receptor (PXR) expression in colorectal cancer cells restricts irinotecan chemosensitivity through enhanced SN-38 glucuronidation. Mol Cancer 9:46PubMedPubMedCentralCrossRef Raynal C, Pascussi JM, Leguelinel G (2010) Pregnane X receptor (PXR) expression in colorectal cancer cells restricts irinotecan chemosensitivity through enhanced SN-38 glucuronidation. Mol Cancer 9:46PubMedPubMedCentralCrossRef
25.
Zurück zum Zitat Grawenda AM, O’Neill E (2015) Clinical utility of RASSF1A methylation in human malignancies. Br J Cancer 113:372–381PubMedCrossRef Grawenda AM, O’Neill E (2015) Clinical utility of RASSF1A methylation in human malignancies. Br J Cancer 113:372–381PubMedCrossRef
26.
Zurück zum Zitat Fiegl H, Millinger S, Mueller-Holzner E, Marth C, Ensinger C, Berger A (2005) Circulating tumor-specific DNA: a marker for monitoring efficacy of adjuvant therapy in cancer patients. Cancer Res 65:1141–1145PubMedCrossRef Fiegl H, Millinger S, Mueller-Holzner E, Marth C, Ensinger C, Berger A (2005) Circulating tumor-specific DNA: a marker for monitoring efficacy of adjuvant therapy in cancer patients. Cancer Res 65:1141–1145PubMedCrossRef
27.
Zurück zum Zitat Gil EY, Jo UH, Jeong H, Whang YM, Woo OH, Cho KR (2012) Promoter methylation of RASSF1A modulates the effect of the microtubule-targeting agent docetaxel in breast cancer. Int J Oncol 41:611–620PubMed Gil EY, Jo UH, Jeong H, Whang YM, Woo OH, Cho KR (2012) Promoter methylation of RASSF1A modulates the effect of the microtubule-targeting agent docetaxel in breast cancer. Int J Oncol 41:611–620PubMed
28.
Zurück zum Zitat Fischer JR, Ohnmacht U, Rieger N, Zemaitis M, Stoffregen C, Manegold C (2007) Prognostic significance of RASSF1A promoter methylation on survival of non-small cell lung cancer patients treated with gemcitabine. Lung Cancer 56:115–123PubMedCrossRef Fischer JR, Ohnmacht U, Rieger N, Zemaitis M, Stoffregen C, Manegold C (2007) Prognostic significance of RASSF1A promoter methylation on survival of non-small cell lung cancer patients treated with gemcitabine. Lung Cancer 56:115–123PubMedCrossRef
29.
Zurück zum Zitat Donson AM, Addo-Yobo SO, Handler MH, Gore L, Foreman NK (2007) MGMT promoter methylation correlates with survival benefit and sensitivity to temozolomide in pediatric glioblastoma. Pediatr Blood Cancer 48:403–407PubMedCrossRef Donson AM, Addo-Yobo SO, Handler MH, Gore L, Foreman NK (2007) MGMT promoter methylation correlates with survival benefit and sensitivity to temozolomide in pediatric glioblastoma. Pediatr Blood Cancer 48:403–407PubMedCrossRef
30.
Zurück zum Zitat Pegg AE (2000) Repair of O6-alkylguanine by alkyltransferases. Mut Res/Rev Mut Res 462:83–100CrossRef Pegg AE (2000) Repair of O6-alkylguanine by alkyltransferases. Mut Res/Rev Mut Res 462:83–100CrossRef
31.
Zurück zum Zitat Von Deimling A, Korshunov A, Hartmann C (2011) The next generation of glioma biomarkers: MGMT methylation, BRAF fusions and IDH1 mutations. Brain Pathol 21:74–87CrossRef Von Deimling A, Korshunov A, Hartmann C (2011) The next generation of glioma biomarkers: MGMT methylation, BRAF fusions and IDH1 mutations. Brain Pathol 21:74–87CrossRef
32.
Zurück zum Zitat Paz MF, Yaya-Tur R, Rojas-Marcos I, Reynes G, Pollan M, Aguirre-Cruz L (2004) CpG island hypermethylation of the DNA repair enzyme methyltransferase predicts response to temozolomide in primary gliomas. Clin Cancer Res 10:4933–4938PubMedCrossRef Paz MF, Yaya-Tur R, Rojas-Marcos I, Reynes G, Pollan M, Aguirre-Cruz L (2004) CpG island hypermethylation of the DNA repair enzyme methyltransferase predicts response to temozolomide in primary gliomas. Clin Cancer Res 10:4933–4938PubMedCrossRef
33.
Zurück zum Zitat Hegi ME, Diserens AC, Godard S, Dietrich PY, Regli L, Ostermann S (2004) Clinical trial substantiates the predictive value of O-6-methylguanine-DNA methyltransferase promoter methylation in glioblastoma patients treated with temozolomide. Clin Cancer Res 10:1871–1874PubMedCrossRef Hegi ME, Diserens AC, Godard S, Dietrich PY, Regli L, Ostermann S (2004) Clinical trial substantiates the predictive value of O-6-methylguanine-DNA methyltransferase promoter methylation in glioblastoma patients treated with temozolomide. Clin Cancer Res 10:1871–1874PubMedCrossRef
34.
Zurück zum Zitat Hegi ME, Diserens AC, Gorlia T, Hamou MF, de Tribolet N, Weller M (2005) MGMT gene silencing and benefit from temozolomide in glioblastoma. N Engl J Med 352:997–1003PubMedCrossRef Hegi ME, Diserens AC, Gorlia T, Hamou MF, de Tribolet N, Weller M (2005) MGMT gene silencing and benefit from temozolomide in glioblastoma. N Engl J Med 352:997–1003PubMedCrossRef
35.
Zurück zum Zitat Everhard S, Kaloshi G, Crinière E, Benouaich-Amiel A, Lejeune J, Marie Y (2006) MGMT methylation: a marker of response to temozolomide in low-grade gliomas. Ann Neurol 60:740–743PubMedCrossRef Everhard S, Kaloshi G, Crinière E, Benouaich-Amiel A, Lejeune J, Marie Y (2006) MGMT methylation: a marker of response to temozolomide in low-grade gliomas. Ann Neurol 60:740–743PubMedCrossRef
36.
Zurück zum Zitat Gerstner ER, Yip S, Wang DL, Louis DN, Iafrate AJ, Batchelor TT (2009) Batchelor, MGMT methylation is a prognostic biomarker in elderly patients with newly diagnosed glioblastoma. Neurology 73:1509–1510PubMedPubMedCentralCrossRef Gerstner ER, Yip S, Wang DL, Louis DN, Iafrate AJ, Batchelor TT (2009) Batchelor, MGMT methylation is a prognostic biomarker in elderly patients with newly diagnosed glioblastoma. Neurology 73:1509–1510PubMedPubMedCentralCrossRef
37.
Zurück zum Zitat Tuominen R, Jewell R, van den Oord JJ, Wolter P, Stierner U, Lindholm C (2015) MGMT promoter methylation is associated with temozolomide response and prolonged progression-free survival in disseminated cutaneous melanoma. Int J Cancer 136:2844–2853PubMedCrossRef Tuominen R, Jewell R, van den Oord JJ, Wolter P, Stierner U, Lindholm C (2015) MGMT promoter methylation is associated with temozolomide response and prolonged progression-free survival in disseminated cutaneous melanoma. Int J Cancer 136:2844–2853PubMedCrossRef
38.
Zurück zum Zitat Agrelo R, Cheng WH, Setien F, Ropero S, Espada J, Fraga MF (2006) Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer. Proc Natl Acad Sci 103:8822–8827PubMedPubMedCentralCrossRef Agrelo R, Cheng WH, Setien F, Ropero S, Espada J, Fraga MF (2006) Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer. Proc Natl Acad Sci 103:8822–8827PubMedPubMedCentralCrossRef
39.
Zurück zum Zitat Scartozzi M, Bearzi I, Mandolesi A, Giampieri R, Faloppi L, Galizia E (2011) Epidermal growth factor receptor (EGFR) gene promoter methylation and cetuximab treatment in colorectal cancer patients. Br J Cancer 104:1786–1790PubMedPubMedCentralCrossRef Scartozzi M, Bearzi I, Mandolesi A, Giampieri R, Faloppi L, Galizia E (2011) Epidermal growth factor receptor (EGFR) gene promoter methylation and cetuximab treatment in colorectal cancer patients. Br J Cancer 104:1786–1790PubMedPubMedCentralCrossRef
40.
Zurück zum Zitat Ebert MP, Tänzer M, Balluff B, Burgermeister E, Kretzschmar AK, Hughes DJ (2012) TFAP2E–DKK4 and chemoresistance in colorectal cancer. N Engl J Med 366:44–53PubMedCrossRef Ebert MP, Tänzer M, Balluff B, Burgermeister E, Kretzschmar AK, Hughes DJ (2012) TFAP2E–DKK4 and chemoresistance in colorectal cancer. N Engl J Med 366:44–53PubMedCrossRef
41.
Zurück zum Zitat Hartmann O, Spyratos F, Harbeck N, Dietrich D, Fassbender A, Schmitt M (2009) DNA methylation markers predict outcome in node-positive, estrogen receptor-positive breast cancer with adjuvant anthracycline-based chemotherapy. Clin Cancer Res 15:315–323PubMedCrossRef Hartmann O, Spyratos F, Harbeck N, Dietrich D, Fassbender A, Schmitt M (2009) DNA methylation markers predict outcome in node-positive, estrogen receptor-positive breast cancer with adjuvant anthracycline-based chemotherapy. Clin Cancer Res 15:315–323PubMedCrossRef
42.
Zurück zum Zitat Iorns E, Turner NC, Elliott R, Syed N, Garrone O, Gasco M (2008) Identification of CDK10 as an important determinant of resistance to endocrine therapy for breast cancer. Cancer Cell 13:91–104PubMedCrossRef Iorns E, Turner NC, Elliott R, Syed N, Garrone O, Gasco M (2008) Identification of CDK10 as an important determinant of resistance to endocrine therapy for breast cancer. Cancer Cell 13:91–104PubMedCrossRef
43.
Zurück zum Zitat Widschwendter M, Siegmund KD, Müller HM, Fiegl H, Marth C, Müller-Holzner E (2004) Association of breast cancer DNA methylation profiles with hormone receptor status and response to tamoxifen. Cancer Res 64:3807–3813PubMedCrossRef Widschwendter M, Siegmund KD, Müller HM, Fiegl H, Marth C, Müller-Holzner E (2004) Association of breast cancer DNA methylation profiles with hormone receptor status and response to tamoxifen. Cancer Res 64:3807–3813PubMedCrossRef
44.
Zurück zum Zitat Chen B, Rao X, House MG, Nephew KP, Cullen KJ, Guo Z (2011) GPx3 promoter hypermethylation is a frequent event in human cancer and is associated with tumorigenesis and chemotherapy response. Cancer Lett 309:37–45PubMedCrossRef Chen B, Rao X, House MG, Nephew KP, Cullen KJ, Guo Z (2011) GPx3 promoter hypermethylation is a frequent event in human cancer and is associated with tumorigenesis and chemotherapy response. Cancer Lett 309:37–45PubMedCrossRef
45.
Zurück zum Zitat Ivanova T, Zouridis H, Wu Y, Cheng LL, Tan IB, Gopalakrishnan V (2013) Integrated epigenomics identifies BMP4 as a modulator of cisplatin sensitivity in gastric cancer. Gut 62:22–33PubMedCrossRef Ivanova T, Zouridis H, Wu Y, Cheng LL, Tan IB, Gopalakrishnan V (2013) Integrated epigenomics identifies BMP4 as a modulator of cisplatin sensitivity in gastric cancer. Gut 62:22–33PubMedCrossRef
46.
Zurück zum Zitat Sun S, Sun P, Wang C, Sun T (2014) Downregulation of microRNA-155 accelerates cell growth and invasion by targeting c-myc in human gastric carcinoma cells. Oncol Rep 32:951–956PubMed Sun S, Sun P, Wang C, Sun T (2014) Downregulation of microRNA-155 accelerates cell growth and invasion by targeting c-myc in human gastric carcinoma cells. Oncol Rep 32:951–956PubMed
47.
Zurück zum Zitat Nana-Sinkam SP, Croce CM (2012) Clinical applications for microRNAs in cancer. Clin Pharmacol Ther 93:98–104PubMedCrossRef Nana-Sinkam SP, Croce CM (2012) Clinical applications for microRNAs in cancer. Clin Pharmacol Ther 93:98–104PubMedCrossRef
48.
Zurück zum Zitat Allen KE, Weiss GJ (2010) Resistance may not be futile: microRNA biomarkers for chemoresistance and potential therapeutics. Mol Cancer Ther 9:3126–3136PubMedCrossRef Allen KE, Weiss GJ (2010) Resistance may not be futile: microRNA biomarkers for chemoresistance and potential therapeutics. Mol Cancer Ther 9:3126–3136PubMedCrossRef
49.
Zurück zum Zitat Volinia S, Calin GA, Liu CG, Ambs S, Cimmino A, Petrocca F (2006) A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 103:2257–2261PubMedPubMedCentralCrossRef Volinia S, Calin GA, Liu CG, Ambs S, Cimmino A, Petrocca F (2006) A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 103:2257–2261PubMedPubMedCentralCrossRef
50.
Zurück zum Zitat Ali S, Ahmad A, Banerjee S, Padhye S, Dominiak K, Schaffert JM (2010) Gemcitabine sensitivity can be induced in pancreatic cancer cells through modulation of miR-200 and miR-21 expression by curcumin or its analogue CDF. Cancer Res 70:3606–3617PubMedPubMedCentralCrossRef Ali S, Ahmad A, Banerjee S, Padhye S, Dominiak K, Schaffert JM (2010) Gemcitabine sensitivity can be induced in pancreatic cancer cells through modulation of miR-200 and miR-21 expression by curcumin or its analogue CDF. Cancer Res 70:3606–3617PubMedPubMedCentralCrossRef
51.
Zurück zum Zitat Giovannetti E, Funel N, Peters GJ, Del Chiaro M, Erozenci LA, Vasile E (2010) MicroRNA-21 in pancreatic cancer: correlation with clinical outcome and pharmacologic aspects underlying its role in the modulation of gemcitabine activity. Cancer Res 70:4528–4538PubMedCrossRef Giovannetti E, Funel N, Peters GJ, Del Chiaro M, Erozenci LA, Vasile E (2010) MicroRNA-21 in pancreatic cancer: correlation with clinical outcome and pharmacologic aspects underlying its role in the modulation of gemcitabine activity. Cancer Res 70:4528–4538PubMedCrossRef
52.
Zurück zum Zitat Gong C, Yao Y, Wang Y, Liu B, Wu W, Chen J (2011) Up-regulation of miR-21 mediates resistance to trastuzumab therapy for breast cancer. J Biol Chem 286:19127–19137PubMedPubMedCentralCrossRef Gong C, Yao Y, Wang Y, Liu B, Wu W, Chen J (2011) Up-regulation of miR-21 mediates resistance to trastuzumab therapy for breast cancer. J Biol Chem 286:19127–19137PubMedPubMedCentralCrossRef
53.
Zurück zum Zitat Echevarría-Vargas IM, Valiyeva F, Vivas-Mejía PE (2014) Upregulation of miR-21 in cisplatin resistant ovarian cancer via JNK-1/c-Jun pathway. PLoS One 9:e97094PubMedPubMedCentralCrossRef Echevarría-Vargas IM, Valiyeva F, Vivas-Mejía PE (2014) Upregulation of miR-21 in cisplatin resistant ovarian cancer via JNK-1/c-Jun pathway. PLoS One 9:e97094PubMedPubMedCentralCrossRef
54.
Zurück zum Zitat Chan JK, Blansit K, Kiet T (2014) The inhibition of miR-21 promotes apoptosis and chemosensitivity in ovarian cancer. Gynecol Oncol 132:739–744PubMedCrossRef Chan JK, Blansit K, Kiet T (2014) The inhibition of miR-21 promotes apoptosis and chemosensitivity in ovarian cancer. Gynecol Oncol 132:739–744PubMedCrossRef
55.
Zurück zum Zitat Schetter AJ, Leung SY, Sohn JJ, Zanetti KA, Bowman ED, Yanaihara N (2008) MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma. JAMA 299:425–436PubMedPubMedCentral Schetter AJ, Leung SY, Sohn JJ, Zanetti KA, Bowman ED, Yanaihara N (2008) MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma. JAMA 299:425–436PubMedPubMedCentral
56.
Zurück zum Zitat Donahue TR, Nguyen AH, Moughan J, Li L, Tatishchev S, Toste P (2014) Stromal MicroRNA-21 levels predict response to 5-fluorouracil in patients with pancreatic cancer. J Surg Oncol 110:952–959PubMedPubMedCentralCrossRef Donahue TR, Nguyen AH, Moughan J, Li L, Tatishchev S, Toste P (2014) Stromal MicroRNA-21 levels predict response to 5-fluorouracil in patients with pancreatic cancer. J Surg Oncol 110:952–959PubMedPubMedCentralCrossRef
57.
Zurück zum Zitat Kurashige J, Kamohara H, Watanabe M, Tanaka Y, Kinoshita K, Saito S (2012) Serum microRNA-21 is a novel biomarker in patients with esophageal squamous cell carcinoma. J Surg Oncol 106:188–192PubMedCrossRef Kurashige J, Kamohara H, Watanabe M, Tanaka Y, Kinoshita K, Saito S (2012) Serum microRNA-21 is a novel biomarker in patients with esophageal squamous cell carcinoma. J Surg Oncol 106:188–192PubMedCrossRef
58.
Zurück zum Zitat Hamano R, Miyata H, Yamasaki M, Kurokawa Y, Hara J, Moon JH (2011) Overexpression of miR-200c induces chemoresistance in esophageal cancers mediated through activation of the Akt signaling pathway. Clin Cancer Res 17:3029–3038PubMedCrossRef Hamano R, Miyata H, Yamasaki M, Kurokawa Y, Hara J, Moon JH (2011) Overexpression of miR-200c induces chemoresistance in esophageal cancers mediated through activation of the Akt signaling pathway. Clin Cancer Res 17:3029–3038PubMedCrossRef
59.
Zurück zum Zitat Cochrane DR, Spoelstra NS, Howe EN, Nordeen SK, Richer JK (2009) MicroRNA-200c mitigates invasiveness and restores sensitivity to microtubule-targeting chemotherapeutic agents. Mol Cancer Ther 8:1055–1066PubMedPubMedCentralCrossRef Cochrane DR, Spoelstra NS, Howe EN, Nordeen SK, Richer JK (2009) MicroRNA-200c mitigates invasiveness and restores sensitivity to microtubule-targeting chemotherapeutic agents. Mol Cancer Ther 8:1055–1066PubMedPubMedCentralCrossRef
60.
Zurück zum Zitat Cittelly DM, Dimitrova I, Howe EN, Cochrane DR, Jean A, Spoelstra NS (2012) Restoration of miR-200c to ovarian cancer reduces tumor burden and increases sensitivity to paclitaxel. Mol Cancer Ther 11:2556–2565PubMedPubMedCentralCrossRef Cittelly DM, Dimitrova I, Howe EN, Cochrane DR, Jean A, Spoelstra NS (2012) Restoration of miR-200c to ovarian cancer reduces tumor burden and increases sensitivity to paclitaxel. Mol Cancer Ther 11:2556–2565PubMedPubMedCentralCrossRef
61.
Zurück zum Zitat Leskelä S, Leandro-García LJ, Mendiola M, Barriuso J, Inglada-Pérez L, Muñoz I (2011) The miR-200 family controls β-tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients. Endocr Relat Cancer 18:85–95PubMedCrossRef Leskelä S, Leandro-García LJ, Mendiola M, Barriuso J, Inglada-Pérez L, Muñoz I (2011) The miR-200 family controls β-tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients. Endocr Relat Cancer 18:85–95PubMedCrossRef
62.
Zurück zum Zitat Chen Y, Sun Y, Chen L, Xu X, Zhang X, Wang B (2013) MiRNA-200c increases the sensitivity of breast cancer cells to doxorubicin through the suppression of E-cadherin-mediated PTEN/Akt signaling. Mol Med Rep 7:1579–1584PubMed Chen Y, Sun Y, Chen L, Xu X, Zhang X, Wang B (2013) MiRNA-200c increases the sensitivity of breast cancer cells to doxorubicin through the suppression of E-cadherin-mediated PTEN/Akt signaling. Mol Med Rep 7:1579–1584PubMed
63.
Zurück zum Zitat Kovalchuk O, Filkowski J, Meservy J (2008) Involvement of microRNA-451 in resistance of the MCF-7 breast cancer cells to chemotherapeutic drug doxorubicin. Mol Cancer Ther 7:2152–2159PubMedCrossRef Kovalchuk O, Filkowski J, Meservy J (2008) Involvement of microRNA-451 in resistance of the MCF-7 breast cancer cells to chemotherapeutic drug doxorubicin. Mol Cancer Ther 7:2152–2159PubMedCrossRef
64.
Zurück zum Zitat Tryndyak VP, Beland FA, Pogribny IP (2010) E-cadherin transcriptional down-regulation by epigenetic and microRNA-200 family alterations is related to mesenchymal and drug-resistant phenotypes in human breast cancer cells. Int J Cancer 126:2575–2583PubMed Tryndyak VP, Beland FA, Pogribny IP (2010) E-cadherin transcriptional down-regulation by epigenetic and microRNA-200 family alterations is related to mesenchymal and drug-resistant phenotypes in human breast cancer cells. Int J Cancer 126:2575–2583PubMed
65.
Zurück zum Zitat Chen J, Tian W, Cai H, He H, Deng Y (2012) Down-regulation of microRNA-200c is associated with drug resistance in human breast cancer. Med Oncol 29:2527–2534PubMedCrossRef Chen J, Tian W, Cai H, He H, Deng Y (2012) Down-regulation of microRNA-200c is associated with drug resistance in human breast cancer. Med Oncol 29:2527–2534PubMedCrossRef
66.
Zurück zum Zitat Alencar AJ, Malumbres R, Kozloski GA, Advani R, Talreja N, Chinichian S (2011) MicroRNAs are independent predictors of outcome in diffuse large B-cell lymphoma patients treated with R-CHOP. Clin Cancer Res 17:4125–4135PubMedPubMedCentralCrossRef Alencar AJ, Malumbres R, Kozloski GA, Advani R, Talreja N, Chinichian S (2011) MicroRNAs are independent predictors of outcome in diffuse large B-cell lymphoma patients treated with R-CHOP. Clin Cancer Res 17:4125–4135PubMedPubMedCentralCrossRef
67.
Zurück zum Zitat Miller TE, Ghoshal K, Ramaswamy B, Roy S, Datta J, Shapiro CL (2008) MicroRNA-221/222 confers tamoxifen resistance in breast cancer by targeting p27Kip1. J Biol Chem 283:29897–29903PubMedPubMedCentralCrossRef Miller TE, Ghoshal K, Ramaswamy B, Roy S, Datta J, Shapiro CL (2008) MicroRNA-221/222 confers tamoxifen resistance in breast cancer by targeting p27Kip1. J Biol Chem 283:29897–29903PubMedPubMedCentralCrossRef
68.
Zurück zum Zitat Gan R, Yang Y, Yang X, Zhao L, Lu J, Meng QH (2014) Downregulation of miR-221/222 enhances sensitivity of breast cancer cells to tamoxifen through upregulation of TIMP3. Cancer Gene Ther 21:290–296PubMedCrossRef Gan R, Yang Y, Yang X, Zhao L, Lu J, Meng QH (2014) Downregulation of miR-221/222 enhances sensitivity of breast cancer cells to tamoxifen through upregulation of TIMP3. Cancer Gene Ther 21:290–296PubMedCrossRef
69.
Zurück zum Zitat Lu YZ, Roy S, Nuovo G, Ramaswamy B, Miller T, Shapiro C (2011) Anti-microRNA-222 (anti-miR-222) and -181B suppress growth of tamoxifen-resistant xenografts in mouse by targeting TIMP3 protein and modulating mitogenic signal. J Biol Chem 286:42292–42302PubMedPubMedCentralCrossRef Lu YZ, Roy S, Nuovo G, Ramaswamy B, Miller T, Shapiro C (2011) Anti-microRNA-222 (anti-miR-222) and -181B suppress growth of tamoxifen-resistant xenografts in mouse by targeting TIMP3 protein and modulating mitogenic signal. J Biol Chem 286:42292–42302PubMedPubMedCentralCrossRef
70.
Zurück zum Zitat Zhao JJ, Lin J, Yang H, Kong W, He L, Ma X (2008) MicroRNA-221/222 negatively regulates estrogen receptor α and is associated with tamoxifen resistance in breast cancer. J Biol Chem 283:31079–31086PubMedPubMedCentralCrossRef Zhao JJ, Lin J, Yang H, Kong W, He L, Ma X (2008) MicroRNA-221/222 negatively regulates estrogen receptor α and is associated with tamoxifen resistance in breast cancer. J Biol Chem 283:31079–31086PubMedPubMedCentralCrossRef
71.
Zurück zum Zitat Jung EJ, Santarpia L, Kim J, Esteva FJ, Moretti E, Buzdar AU (2012) Plasma microRNA 210 levels correlate with sensitivity to trastuzumab and tumor presence in breast cancer patients. Cancer 118:2603–2614PubMedCrossRef Jung EJ, Santarpia L, Kim J, Esteva FJ, Moretti E, Buzdar AU (2012) Plasma microRNA 210 levels correlate with sensitivity to trastuzumab and tumor presence in breast cancer patients. Cancer 118:2603–2614PubMedCrossRef
72.
Zurück zum Zitat Rothé F, Ignatiadis M, Chaboteaux C, Haibe-Kains B, Kheddoumi N, Majjaj S (2011) Global microRNA expression profiling identifies miR-210 associated with tumor proliferation, invasion and poor clinical outcome in breast cancer. PLoS One 6:20980CrossRef Rothé F, Ignatiadis M, Chaboteaux C, Haibe-Kains B, Kheddoumi N, Majjaj S (2011) Global microRNA expression profiling identifies miR-210 associated with tumor proliferation, invasion and poor clinical outcome in breast cancer. PLoS One 6:20980CrossRef
73.
Zurück zum Zitat Chen J, Wang W, Zhang Y, Chen Y, Hu T (2014) Predicting distant metastasis and chemoresistance using plasma miRNAs. Med Oncol 31:1–7 Chen J, Wang W, Zhang Y, Chen Y, Hu T (2014) Predicting distant metastasis and chemoresistance using plasma miRNAs. Med Oncol 31:1–7
74.
Zurück zum Zitat Mei Y, Gao C, Wang K, Cui L, Li W, Zhao X (2014) Effect of microRNA-210 on prognosis and response to chemotherapeutic drugs in pediatric acute lymphoblastic leukemia. Cancer Sci 105:463–472PubMedPubMedCentralCrossRef Mei Y, Gao C, Wang K, Cui L, Li W, Zhao X (2014) Effect of microRNA-210 on prognosis and response to chemotherapeutic drugs in pediatric acute lymphoblastic leukemia. Cancer Sci 105:463–472PubMedPubMedCentralCrossRef
75.
Zurück zum Zitat Zhang T, Wang Q, Zhao D, Cui Y, Cao B, Guo L (2011) The oncogenetic role of microRNA-31 as a potential biomarker in oesophageal squamous cell carcinoma. Clin Sci 121:437–447PubMedCrossRef Zhang T, Wang Q, Zhao D, Cui Y, Cao B, Guo L (2011) The oncogenetic role of microRNA-31 as a potential biomarker in oesophageal squamous cell carcinoma. Clin Sci 121:437–447PubMedCrossRef
76.
Zurück zum Zitat Bhatnagar N, Li X, Padi SK, Zhang Q, Tang MS, Guo B (2010) Downregulation of miR-205 and miR-31 confers resistance to chemotherapy-induced apoptosis in prostate cancer cells. Cell Death Dis 1:e105PubMedPubMedCentralCrossRef Bhatnagar N, Li X, Padi SK, Zhang Q, Tang MS, Guo B (2010) Downregulation of miR-205 and miR-31 confers resistance to chemotherapy-induced apoptosis in prostate cancer cells. Cell Death Dis 1:e105PubMedPubMedCentralCrossRef
77.
Zurück zum Zitat Mitamura T, Watari H, Wang L, Kanno H, Hassan MK, Miyazaki M (2013) Downregulation of miRNA-31 induces taxane resistance in ovarian cancer cells through increase of receptor tyrosine kinase MET. Oncogenesis 2:e40PubMedPubMedCentralCrossRef Mitamura T, Watari H, Wang L, Kanno H, Hassan MK, Miyazaki M (2013) Downregulation of miRNA-31 induces taxane resistance in ovarian cancer cells through increase of receptor tyrosine kinase MET. Oncogenesis 2:e40PubMedPubMedCentralCrossRef
78.
Zurück zum Zitat Dong Z, Zhong Z, Yang L, Wang S, Gong Z (2014) MicroRNA-31 inhibits cisplatin-induced apoptosis in non-small cell lung cancer cells by regulating the drug transporter ABCB9. Cancer Lett 343:249–257PubMedCrossRef Dong Z, Zhong Z, Yang L, Wang S, Gong Z (2014) MicroRNA-31 inhibits cisplatin-induced apoptosis in non-small cell lung cancer cells by regulating the drug transporter ABCB9. Cancer Lett 343:249–257PubMedCrossRef
79.
Zurück zum Zitat Wang CJ, Stratmann J, Zhou ZG, Sun XF (2010) Suppression of microRNA-31 increases sensitivity to 5-FU at an early stage, and affects cell migration and invasion in HCT-116 colon cancer cells. BMC Cancer 10:616PubMedPubMedCentralCrossRef Wang CJ, Stratmann J, Zhou ZG, Sun XF (2010) Suppression of microRNA-31 increases sensitivity to 5-FU at an early stage, and affects cell migration and invasion in HCT-116 colon cancer cells. BMC Cancer 10:616PubMedPubMedCentralCrossRef
80.
81.
Zurück zum Zitat Dawson MA, Kouzarides T (2012) Cancer epigenetics: from mechanism to therapy. Cell 150:12–27PubMedCrossRef Dawson MA, Kouzarides T (2012) Cancer epigenetics: from mechanism to therapy. Cell 150:12–27PubMedCrossRef
83.
Zurück zum Zitat Hu S, Yu L, Li Z, Shen Y, Wang J, Cai J (2010) Overexpression of EZH2 contributes to acquired cisplatin resistance in ovarian cancer cells in vitro and in vivo. Cancer Biol Ther 10:788–795PubMedCrossRef Hu S, Yu L, Li Z, Shen Y, Wang J, Cai J (2010) Overexpression of EZH2 contributes to acquired cisplatin resistance in ovarian cancer cells in vitro and in vivo. Cancer Biol Ther 10:788–795PubMedCrossRef
84.
Zurück zum Zitat Cai MY, Tong ZT, Zhu W, Wen ZZ, Rao HL, Kong LL (2011) H3K27me3 protein is a promising predictive biomarker of patients’ survival and chemoradioresistance in human nasopharyngeal carcinoma. Mol Med 17:1137PubMedPubMedCentral Cai MY, Tong ZT, Zhu W, Wen ZZ, Rao HL, Kong LL (2011) H3K27me3 protein is a promising predictive biomarker of patients’ survival and chemoradioresistance in human nasopharyngeal carcinoma. Mol Med 17:1137PubMedPubMedCentral
85.
Zurück zum Zitat He LR, Liu MZ, Li BK, Rao HL, Liao YJ, Guan XY (2009) Prognostic impact of H3K27me3 expression on locoregional progression after chemoradiotherapy in esophageal squamous cell carcinoma. BMC Cancer 9:461PubMedPubMedCentralCrossRef He LR, Liu MZ, Li BK, Rao HL, Liao YJ, Guan XY (2009) Prognostic impact of H3K27me3 expression on locoregional progression after chemoradiotherapy in esophageal squamous cell carcinoma. BMC Cancer 9:461PubMedPubMedCentralCrossRef
86.
Zurück zum Zitat Abbosh PH, Montgomery JS, Starkey JA, Novotny M, Zuhowski EG, Egorin MJ (2006) Dominant-negative histone H3 lysine 27 mutant derepresses silenced tumor suppressor genes and reverses the drug-resistant phenotype in cancer cells. Cancer Res 66:5582–5591PubMedCrossRef Abbosh PH, Montgomery JS, Starkey JA, Novotny M, Zuhowski EG, Egorin MJ (2006) Dominant-negative histone H3 lysine 27 mutant derepresses silenced tumor suppressor genes and reverses the drug-resistant phenotype in cancer cells. Cancer Res 66:5582–5591PubMedCrossRef
87.
Zurück zum Zitat Manuyakorn A, Paulus R, Farrell J, Dawson NA, Tze S, Cellular Cheung-Lau G (2010) Histone modification patterns predict prognosis and treatment response in resectable pancreatic adenocarcinoma: results from RTOG 9704. J Clin Oncol 28:1358–1365PubMedPubMedCentralCrossRef Manuyakorn A, Paulus R, Farrell J, Dawson NA, Tze S, Cellular Cheung-Lau G (2010) Histone modification patterns predict prognosis and treatment response in resectable pancreatic adenocarcinoma: results from RTOG 9704. J Clin Oncol 28:1358–1365PubMedPubMedCentralCrossRef
88.
Zurück zum Zitat Watanabe T, Morinaga S, Akaike M, Numata M, Tamagawa H, Yamamoto N (2012) The cellular level of histone H3 lysine 4 dimethylation correlates with response to adjuvant gemcitabine in Japanese pancreatic cancer patients treated with surgery. Eur J Surg Oncol (EJSO) 38:1051–1057CrossRef Watanabe T, Morinaga S, Akaike M, Numata M, Tamagawa H, Yamamoto N (2012) The cellular level of histone H3 lysine 4 dimethylation correlates with response to adjuvant gemcitabine in Japanese pancreatic cancer patients treated with surgery. Eur J Surg Oncol (EJSO) 38:1051–1057CrossRef
89.
Zurück zum Zitat Sakamoto K, Imamura T, Yano M, Yoshida H, Fujiki A, Hirashima Y, Hosoi H (2014) Sensitivity of MLL-rearranged AML cells to all-trans retinoic acid is associated with the level of H3K4me2 in the RARα promoter region. Blood Cancer J 4:e205PubMedPubMedCentralCrossRef Sakamoto K, Imamura T, Yano M, Yoshida H, Fujiki A, Hirashima Y, Hosoi H (2014) Sensitivity of MLL-rearranged AML cells to all-trans retinoic acid is associated with the level of H3K4me2 in the RARα promoter region. Blood Cancer J 4:e205PubMedPubMedCentralCrossRef
90.
Zurück zum Zitat Hou J, Wu J, Dombkowski A, Zhang K, Holowatyj A, Boerner JL (2012) Genomic amplification and a role in drug-resistance for the KDM5A histone demethylase in breast cancer. Am J Transl Res 4:247PubMedPubMedCentral Hou J, Wu J, Dombkowski A, Zhang K, Holowatyj A, Boerner JL (2012) Genomic amplification and a role in drug-resistance for the KDM5A histone demethylase in breast cancer. Am J Transl Res 4:247PubMedPubMedCentral
91.
Zurück zum Zitat Toth M, Boros IM, Balint E (2012) Elevated level of lysine 9-acetylated histone H3 at the MDR1 promoter in multidrug-resistant cells. Cancer Sci 103:659–669PubMedCrossRef Toth M, Boros IM, Balint E (2012) Elevated level of lysine 9-acetylated histone H3 at the MDR1 promoter in multidrug-resistant cells. Cancer Sci 103:659–669PubMedCrossRef
92.
Zurück zum Zitat Kitange GJ, Mladek AC, Carlson BL, Schroeder MA, Pokorny JL, Cen L (2012) Inhibition of histone deacetylation potentiates the evolution of acquired temozolomide resistance linked to MGMT upregulation in glioblastoma xenografts. Clin Cancer Res 18:4070–4079PubMedPubMedCentralCrossRef Kitange GJ, Mladek AC, Carlson BL, Schroeder MA, Pokorny JL, Cen L (2012) Inhibition of histone deacetylation potentiates the evolution of acquired temozolomide resistance linked to MGMT upregulation in glioblastoma xenografts. Clin Cancer Res 18:4070–4079PubMedPubMedCentralCrossRef
93.
Zurück zum Zitat Chang J, Varghese DS, Gillam MC, Peyton M, Modi B, Schiltz RL (2011) Differential response of cancer cells to HDAC inhibitors trichostatin A and depsipeptide. Br J Cancer 106:116–125PubMedPubMedCentralCrossRef Chang J, Varghese DS, Gillam MC, Peyton M, Modi B, Schiltz RL (2011) Differential response of cancer cells to HDAC inhibitors trichostatin A and depsipeptide. Br J Cancer 106:116–125PubMedPubMedCentralCrossRef
94.
Zurück zum Zitat McDonald KL, Rapkins RW, Olivier J (2013) The T genotype of the MGMT C> T (rs16906252) enhancer single-nucleotide polymorphism (SNP) is associated with promoter methylation and longer survival in glioblastoma patients. Eur J Cancer 49:360–368PubMedCrossRef McDonald KL, Rapkins RW, Olivier J (2013) The T genotype of the MGMT C> T (rs16906252) enhancer single-nucleotide polymorphism (SNP) is associated with promoter methylation and longer survival in glioblastoma patients. Eur J Cancer 49:360–368PubMedCrossRef
95.
Zurück zum Zitat Rapkins RW, Wang F, Nguyen HTN (2015) The MGMT promoter SNP rs16906252 is a risk factor for MGMT methylation in glioblastoma and is predictive of response to temozolomide. Neuro-oncology 17:1589–1598PubMedCrossRef Rapkins RW, Wang F, Nguyen HTN (2015) The MGMT promoter SNP rs16906252 is a risk factor for MGMT methylation in glioblastoma and is predictive of response to temozolomide. Neuro-oncology 17:1589–1598PubMedCrossRef
96.
Zurück zum Zitat Deng Y, Bai H, Hu H (2015) Rs11671784 G/A variation in miR-27a decreases chemo-sensitivity of bladder cancer by decreasing miR-27a and increasing the target RUNX-1 expression. Biochem Biophys Res Commun 458:321–327PubMedCrossRef Deng Y, Bai H, Hu H (2015) Rs11671784 G/A variation in miR-27a decreases chemo-sensitivity of bladder cancer by decreasing miR-27a and increasing the target RUNX-1 expression. Biochem Biophys Res Commun 458:321–327PubMedCrossRef
97.
Zurück zum Zitat Marschner N, Arnold D, Engel E, Hutzschenreuter U, Rauh J, Freier W (2008) Genetic variants of miRNA sequences and non-small cell lung cancer survival. J Clin Investig 118:2600 Marschner N, Arnold D, Engel E, Hutzschenreuter U, Rauh J, Freier W (2008) Genetic variants of miRNA sequences and non-small cell lung cancer survival. J Clin Investig 118:2600
98.
Zurück zum Zitat Zhan X, Wu W, Han B (2012) Has-miR-196a2 functional SNP is associated with severe toxicity after platinum-based chemotherapy of advanced nonsmall cell lung cancer patients in a Chinese population. J Clin Lab Anal 26:441–446PubMedCrossRef Zhan X, Wu W, Han B (2012) Has-miR-196a2 functional SNP is associated with severe toxicity after platinum-based chemotherapy of advanced nonsmall cell lung cancer patients in a Chinese population. J Clin Lab Anal 26:441–446PubMedCrossRef
99.
Zurück zum Zitat Boni V, Zarate R, Villa JC (2011) Role of primary miRNA polymorphic variants in metastatic colon cancer patients treated with 5-fluorouracil and irinotecan. Pharmacogenomics J 11:429–436PubMedCrossRef Boni V, Zarate R, Villa JC (2011) Role of primary miRNA polymorphic variants in metastatic colon cancer patients treated with 5-fluorouracil and irinotecan. Pharmacogenomics J 11:429–436PubMedCrossRef
100.
Zurück zum Zitat Thomadaki H, Talieri M, Scorilas A (2006) Treatment of MCF-7 cells with taxol and etoposide induces distinct alterations in the expression of apoptosis-related genes BCL2, BCL2L12, BAX, CASPASE-9 and FAS. Biol Chem 387:1081–1086PubMedCrossRef Thomadaki H, Talieri M, Scorilas A (2006) Treatment of MCF-7 cells with taxol and etoposide induces distinct alterations in the expression of apoptosis-related genes BCL2, BCL2L12, BAX, CASPASE-9 and FAS. Biol Chem 387:1081–1086PubMedCrossRef
101.
Zurück zum Zitat Wang T, Huang B, Guo R (2015) A let-7b binding site SNP in the 3′-UTR of the Bcl-xL gene enhances resistance to 5-fluorouracil and doxorubicin in breast cancer cells. Oncol Lett 9:1907–1911PubMedPubMedCentral Wang T, Huang B, Guo R (2015) A let-7b binding site SNP in the 3′-UTR of the Bcl-xL gene enhances resistance to 5-fluorouracil and doxorubicin in breast cancer cells. Oncol Lett 9:1907–1911PubMedPubMedCentral
102.
Zurück zum Zitat McDonald KL, Aw G, Kleihues P (2012) Role of biomarkers in the clinical management of glioblastomas: what are the barriers and how can we overcome them? Front Neurol 3:188PubMedPubMedCentral McDonald KL, Aw G, Kleihues P (2012) Role of biomarkers in the clinical management of glioblastomas: what are the barriers and how can we overcome them? Front Neurol 3:188PubMedPubMedCentral
103.
Zurück zum Zitat MDxHealth (2012) MDxHealth signs worldwide development and commercialization agreement with Merck KGaA for MGMT diagnostic test 5 July 2012 MDxHealth (2012) MDxHealth signs worldwide development and commercialization agreement with Merck KGaA for MGMT diagnostic test 5 July 2012
104.
Zurück zum Zitat Imanaka Y, Tsuchiya S, Sato F, Shimada Y, Shimizu K, Tsujimoto G (2011) MicroRNA-141 confers resistance to cisplatin-induced apoptosis by targeting YAP1 in human esophageal squamous cell carcinoma. J Hum Genet 56:270–276PubMedCrossRef Imanaka Y, Tsuchiya S, Sato F, Shimada Y, Shimizu K, Tsujimoto G (2011) MicroRNA-141 confers resistance to cisplatin-induced apoptosis by targeting YAP1 in human esophageal squamous cell carcinoma. J Hum Genet 56:270–276PubMedCrossRef
105.
Zurück zum Zitat Fu X, Tian J, Zhang L, Chen Y, Hao Q (2012) Involvement of microRNA-93, a new regulator of PTEN/Akt signaling pathway, in regulation of chemotherapeutic drug cisplatin chemosensitivity in ovarian cancer cells. FEBS Lett 586:1279–1286PubMedCrossRef Fu X, Tian J, Zhang L, Chen Y, Hao Q (2012) Involvement of microRNA-93, a new regulator of PTEN/Akt signaling pathway, in regulation of chemotherapeutic drug cisplatin chemosensitivity in ovarian cancer cells. FEBS Lett 586:1279–1286PubMedCrossRef
106.
Zurück zum Zitat Zhao Z, Zhang L, Yao Q, Tao Z (2015) MiR-15b regulates cisplatin resistance and metastasis by targeting PEBP4 in human lung adenocarcinoma cells. Cancer Gene Ther 22:108–114PubMedCrossRef Zhao Z, Zhang L, Yao Q, Tao Z (2015) MiR-15b regulates cisplatin resistance and metastasis by targeting PEBP4 in human lung adenocarcinoma cells. Cancer Gene Ther 22:108–114PubMedCrossRef
107.
Zurück zum Zitat Nordentoft I, Birkenkamp-Demtroder K, Agerbæk M, Theodorescu D, Ostenfeld MS, Hartmann A (2012) MiRNAs associated with chemo-sensitivity in cell lines and in advanced bladder cancer. BMC Med Genomics 5:40PubMedPubMedCentralCrossRef Nordentoft I, Birkenkamp-Demtroder K, Agerbæk M, Theodorescu D, Ostenfeld MS, Hartmann A (2012) MiRNAs associated with chemo-sensitivity in cell lines and in advanced bladder cancer. BMC Med Genomics 5:40PubMedPubMedCentralCrossRef
108.
Zurück zum Zitat De Cecco L, Berardi M, Sommariva M, Cataldo A, Canevari S, Mezzanzanica D (2013) Increased sensitivity to chemotherapy induced by CpG-ODN treatment is mediated by microRNA modulation. PLoS One 8:e58849PubMedPubMedCentralCrossRef De Cecco L, Berardi M, Sommariva M, Cataldo A, Canevari S, Mezzanzanica D (2013) Increased sensitivity to chemotherapy induced by CpG-ODN treatment is mediated by microRNA modulation. PLoS One 8:e58849PubMedPubMedCentralCrossRef
109.
Zurück zum Zitat Li B, Chen H, Wu N (2014) Deregulation of miR-128 in ovarian cancer promotes cisplatin resistance. Int J Gynecol Cancer 24(8):1381–1388PubMedCrossRef Li B, Chen H, Wu N (2014) Deregulation of miR-128 in ovarian cancer promotes cisplatin resistance. Int J Gynecol Cancer 24(8):1381–1388PubMedCrossRef
110.
Zurück zum Zitat Zhu W, Xu H, Zhu D, Zhi H, Wang T, Wang J (2012) MiR-200bc/429 cluster modulates multidrug resistance of human cancer cell lines by targeting BCL2 and XIAP. Cancer Chemother Pharmacol 69:723–731PubMedCrossRef Zhu W, Xu H, Zhu D, Zhi H, Wang T, Wang J (2012) MiR-200bc/429 cluster modulates multidrug resistance of human cancer cell lines by targeting BCL2 and XIAP. Cancer Chemother Pharmacol 69:723–731PubMedCrossRef
111.
Zurück zum Zitat Xia L, Zhang D, Du R, Pan Y, Zhao L, Sun S (2008) MiR-15b and miR-16 modulate multidrug resistance by targeting BCL2 in human gastric cancer cells. Int J Cancer 123:372–379PubMedCrossRef Xia L, Zhang D, Du R, Pan Y, Zhao L, Sun S (2008) MiR-15b and miR-16 modulate multidrug resistance by targeting BCL2 in human gastric cancer cells. Int J Cancer 123:372–379PubMedCrossRef
112.
Zurück zum Zitat Zhu Y, Yu F, Jiao Y, Feng J, Tang W, Yao H (2012) MiR-34a predicts survival of Ewing’s sarcoma patients and directly influences cell chemo-sensitivity and malignancy. J Pathol 226:796–805CrossRef Zhu Y, Yu F, Jiao Y, Feng J, Tang W, Yao H (2012) MiR-34a predicts survival of Ewing’s sarcoma patients and directly influences cell chemo-sensitivity and malignancy. J Pathol 226:796–805CrossRef
113.
Zurück zum Zitat Zhu Y, Yu F, Jiao Y, Feng J, Tang W, Yao H (2011) Reduced miR-128 in breast tumor–initiating cells induces chemotherapeutic resistance via Bmi-1 and ABCC5. Clin Cancer Res 17:7105–7115PubMedCrossRef Zhu Y, Yu F, Jiao Y, Feng J, Tang W, Yao H (2011) Reduced miR-128 in breast tumor–initiating cells induces chemotherapeutic resistance via Bmi-1 and ABCC5. Clin Cancer Res 17:7105–7115PubMedCrossRef
114.
Zurück zum Zitat Tormo E, Pineda B, Serna E, Guijarro A, Ribas G, Fores J (2015) MicroRNA profile in response to doxorubicin treatment in breast cancer. J Cell Biochem 116:2061–2073PubMedCrossRef Tormo E, Pineda B, Serna E, Guijarro A, Ribas G, Fores J (2015) MicroRNA profile in response to doxorubicin treatment in breast cancer. J Cell Biochem 116:2061–2073PubMedCrossRef
115.
Zurück zum Zitat Yao YS, Qiu WS, Yao RY (2015) MiR-141 confers docetaxel chemoresistance of breast cancer cells via regulation of EIF4E expression. Oncol Rep 33:2504–2512PubMed Yao YS, Qiu WS, Yao RY (2015) MiR-141 confers docetaxel chemoresistance of breast cancer cells via regulation of EIF4E expression. Oncol Rep 33:2504–2512PubMed
116.
Zurück zum Zitat Butrym A, Rybka J, Baczyńska D, Tukiendorf A, Kuliczkowski K, Mazur G (2015) Expression of microRNA-331 can be used as a predictor for response to therapy and survival in acute myeloid leukemia patients. Biomark Med 9:1–8CrossRef Butrym A, Rybka J, Baczyńska D, Tukiendorf A, Kuliczkowski K, Mazur G (2015) Expression of microRNA-331 can be used as a predictor for response to therapy and survival in acute myeloid leukemia patients. Biomark Med 9:1–8CrossRef
117.
Zurück zum Zitat Xue J, Chi Y, Chen Y, Huang S, Ye X, Niu J (2015) MiRNA-621 sensitizes breast cancer to chemotherapy by suppressing FBXO11 and enhancing p53 activity. Oncogene 96:1–11 Xue J, Chi Y, Chen Y, Huang S, Ye X, Niu J (2015) MiRNA-621 sensitizes breast cancer to chemotherapy by suppressing FBXO11 and enhancing p53 activity. Oncogene 96:1–11
118.
Zurück zum Zitat Akçakaya P, Caramuta S, Åhlen J, Ghaderi M, Berglund E, Östman A (2014) MicroRNA expression signatures of gastrointestinal stromal tumours: associations with imatinib resistance and patient outcome. Br J Cancer 111:2091–2102PubMedPubMedCentralCrossRef Akçakaya P, Caramuta S, Åhlen J, Ghaderi M, Berglund E, Östman A (2014) MicroRNA expression signatures of gastrointestinal stromal tumours: associations with imatinib resistance and patient outcome. Br J Cancer 111:2091–2102PubMedPubMedCentralCrossRef
Metadaten
Titel
Epigenetic alternations and cancer chemotherapy response
verfasst von
Jin-Feng Lv
Lei Hu
Wei Zhuo
Cong-Min Zhang
Hong-Hao Zhou
Lan Fan
Publikationsdatum
26.12.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Cancer Chemotherapy and Pharmacology / Ausgabe 4/2016
Print ISSN: 0344-5704
Elektronische ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-015-2951-0

Weitere Artikel der Ausgabe 4/2016

Cancer Chemotherapy and Pharmacology 4/2016 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.