Skip to main content
Erschienen in: Cancer Chemotherapy and Pharmacology 5/2013

01.05.2013 | Original Article

Regulation of microtubule-associated protein tau (MAPT) by miR-34c-5p determines the chemosensitivity of gastric cancer to paclitaxel

verfasst von: Hao Wu, Min Huang, Mingjie Lu, Wei Zhu, Yongqian Shu, Peng Cao, Ping Liu

Erschienen in: Cancer Chemotherapy and Pharmacology | Ausgabe 5/2013

Einloggen, um Zugang zu erhalten

Abstract

Background

Human miR-34c has been reported to be associated with various human malignancies; however, it remains unknown whether miR-34c is involved in chemoresistance in gastric cancer. The aim of this study was to investigate the role of miR-34c in gastric cancer.

Materials and methods

The adenosine triphosphate-based tumor chemosensitivity assay was used to measure drug sensitivity in gastric cancer samples. The expression levels of miRNA were determined by reverse transcriptase polymerase chain reaction (PCR) and those of protein were by Western blot analysis. Luciferase activity assay was used to verify the target genes of miRNAs. MTT assay was used to test the drug-resistant phenotype changes in cancer cells via overregulation of miRNAs. The methylation status of neighboring CpG islands of miR-34c-5p was analyzed by Bisulfite Sequencing PCR and methylation-specific PCR.

Results

Quantitative real-time polymerase chain reaction demonstrated that expression of miR-34c-5p was downregulated in paclitaxel-resistant gastric cancer samples (p < 0.01). Cells derived from gastric cancer tissues with low miR-34c-5p expression and high microtubule-associated protein tau (MAPT) protein expression tended to have increased chemoresistance to paclitaxel in vitro. Luciferase activity assay confirmed that the 3′-UTR of MAPT mRNA contains a functional miR-34c-5p binding site. Overexpression of miR-34c-5p significantly downregulated MAPT protein expression and increased the chemosensitivity of paclitaxel-resistant gastric cancer cells. Further investigation demonstrated that differential methylation of CpG islands neighboring the miR-34c promoter regulated the expression of miR-34c-5p in gastric cancer cell lines.

Conclusions

DNA methylation, dysregulation of miR-34c-5p, and MAPT expression are critical factors in the chemoresistance of gastric cancer to paclitaxel.
Literatur
1.
Zurück zum Zitat Jemal A, Bray F, Center MM, Ferlay J, Ward E et al (2011) Global cancer statistics. CA Cancer J Clin 61:69–90PubMedCrossRef Jemal A, Bray F, Center MM, Ferlay J, Ward E et al (2011) Global cancer statistics. CA Cancer J Clin 61:69–90PubMedCrossRef
2.
Zurück zum Zitat Ajani JA, Barthel JS, Bekaii-Saab T, Bentrem DJ, D’Amico TA et al (2010) NCCN gastric cancer panel. Gastric cancer. J Natl Compr Canc Netw 8:378–409PubMed Ajani JA, Barthel JS, Bekaii-Saab T, Bentrem DJ, D’Amico TA et al (2010) NCCN gastric cancer panel. Gastric cancer. J Natl Compr Canc Netw 8:378–409PubMed
3.
Zurück zum Zitat Ajani JA, Moiseyenko VM, Tjulandin S, Majlis A, Constenla M et al (2007) Quality of life with docetaxel plus cisplatin and fluorouracil compared with cisplatin and fluorouracil from a phase III trial for advanced gastric or gastroesophageal adenocarcinoma: the V-325 Study Group. J Clin Oncol 25:3210–3216PubMedCrossRef Ajani JA, Moiseyenko VM, Tjulandin S, Majlis A, Constenla M et al (2007) Quality of life with docetaxel plus cisplatin and fluorouracil compared with cisplatin and fluorouracil from a phase III trial for advanced gastric or gastroesophageal adenocarcinoma: the V-325 Study Group. J Clin Oncol 25:3210–3216PubMedCrossRef
4.
Zurück zum Zitat Takeyoshi I, Makita F, Tanahashi Y, Iwazaki S, Ogawa T et al (2011) A phase II study of weekly paclitaxel and doxifluridine combination chemotherapy for advanced/recurrent gastric cancer. Anticancer Res 31:287–291PubMed Takeyoshi I, Makita F, Tanahashi Y, Iwazaki S, Ogawa T et al (2011) A phase II study of weekly paclitaxel and doxifluridine combination chemotherapy for advanced/recurrent gastric cancer. Anticancer Res 31:287–291PubMed
5.
Zurück zum Zitat Ludwig AH, Kupryjañczyk J (2006) Does MDR-1 G2677T/A polymorphism really associate with ovarian cancer response to paclitaxel chemotherapy? Clin Cancer Res 12:6204PubMedCrossRef Ludwig AH, Kupryjañczyk J (2006) Does MDR-1 G2677T/A polymorphism really associate with ovarian cancer response to paclitaxel chemotherapy? Clin Cancer Res 12:6204PubMedCrossRef
6.
Zurück zum Zitat Gao J, Lu M, Yu JW, Li YY, Shen L (2011) Thymidine phosphorylase/β-tubulin III expressions predict the response in Chinese advanced gastric cancer patients receiving first-line capecitabine plus paclitaxel. BMC Cancer 11:177PubMedCrossRef Gao J, Lu M, Yu JW, Li YY, Shen L (2011) Thymidine phosphorylase/β-tubulin III expressions predict the response in Chinese advanced gastric cancer patients receiving first-line capecitabine plus paclitaxel. BMC Cancer 11:177PubMedCrossRef
7.
Zurück zum Zitat Yusuf RZ, Duan Z, Lamendola DE, Penson RT, Seiden MV (2003) Paclitaxel resistance: molecular mechanisms and pharmacologic manipulation. Curr Cancer Drug Targets 3:1–19PubMedCrossRef Yusuf RZ, Duan Z, Lamendola DE, Penson RT, Seiden MV (2003) Paclitaxel resistance: molecular mechanisms and pharmacologic manipulation. Curr Cancer Drug Targets 3:1–19PubMedCrossRef
8.
Zurück zum Zitat Wagner P, Wang B, Clark E, Lee H, Rouzier R, Pusztai L (2005) Microtubule-associated protein (MAP)-Tau: a novel mediator of paclitaxel sensitivity in vitro and in vivo. Cell Cycle 4:1149–1152PubMedCrossRef Wagner P, Wang B, Clark E, Lee H, Rouzier R, Pusztai L (2005) Microtubule-associated protein (MAP)-Tau: a novel mediator of paclitaxel sensitivity in vitro and in vivo. Cell Cycle 4:1149–1152PubMedCrossRef
9.
Zurück zum Zitat Li QQ, Cao XX, Xu JD, Chen Q, Wang WJ et al (2009) The role of P-glycoprotein/cellular prion protein interaction in multidrug-resistant breast cancer cells treated with paclitaxel. Cell Mol Life Sci 66:504–515PubMedCrossRef Li QQ, Cao XX, Xu JD, Chen Q, Wang WJ et al (2009) The role of P-glycoprotein/cellular prion protein interaction in multidrug-resistant breast cancer cells treated with paclitaxel. Cell Mol Life Sci 66:504–515PubMedCrossRef
10.
Zurück zum Zitat Ouzier R, Rajan R, Wagner P, Hess KR, Gold DL et al (2005) Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci USA 102:8315–8320CrossRef Ouzier R, Rajan R, Wagner P, Hess KR, Gold DL et al (2005) Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci USA 102:8315–8320CrossRef
11.
Zurück zum Zitat Smoter M, Bodnar L, Duchnowska R, Stec R, Grala B et al (2011) The role of Tau protein in resistance to paclitaxel. Cancer Chemother Pharmacol 68:553–557PubMedCrossRef Smoter M, Bodnar L, Duchnowska R, Stec R, Grala B et al (2011) The role of Tau protein in resistance to paclitaxel. Cancer Chemother Pharmacol 68:553–557PubMedCrossRef
12.
Zurück zum Zitat Drechsel DN, Hyman AA, Cobb MH, Kirschner MW (1992) Modulation of the dynamic instability of tubulin assembly by the microtubule-associated protein tau. Mol Biol Cell 3:1141–1154PubMed Drechsel DN, Hyman AA, Cobb MH, Kirschner MW (1992) Modulation of the dynamic instability of tubulin assembly by the microtubule-associated protein tau. Mol Biol Cell 3:1141–1154PubMed
13.
Zurück zum Zitat Mimori K, Sadanaga N, Yoshikawa Y, Ishikawa K, Hashimoto M et al (2006) Reduced tau expression in gastric cancer can identify candidates for successful paclitaxel treatment. Br J Cancer 94:1894–1897PubMedCrossRef Mimori K, Sadanaga N, Yoshikawa Y, Ishikawa K, Hashimoto M et al (2006) Reduced tau expression in gastric cancer can identify candidates for successful paclitaxel treatment. Br J Cancer 94:1894–1897PubMedCrossRef
14.
Zurück zum Zitat Zheng T, Wang J, Chen X, Liu L (2010) Role of microRNA in anticancer drug resistance. Int J Cancer 126:2–10PubMedCrossRef Zheng T, Wang J, Chen X, Liu L (2010) Role of microRNA in anticancer drug resistance. Int J Cancer 126:2–10PubMedCrossRef
15.
Zurück zum Zitat Hummel R, Hussey DJ, Haier J (2010) MicroRNAs: predictors and modifiers of chemo- and radiotherapy in different tumour types. Eur J Cancer 46:298–311PubMedCrossRef Hummel R, Hussey DJ, Haier J (2010) MicroRNAs: predictors and modifiers of chemo- and radiotherapy in different tumour types. Eur J Cancer 46:298–311PubMedCrossRef
16.
17.
Zurück zum Zitat Lee Rosalind C, Feinbaum Rhonda L, Ambros Victor (1993) The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell 75:843–854PubMedCrossRef Lee Rosalind C, Feinbaum Rhonda L, Ambros Victor (1993) The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell 75:843–854PubMedCrossRef
18.
Zurück zum Zitat Sarkar Fazlul H, Li Yiwei, Wang Zhiwei, Kong Dejuan et al (2010) Implication of microRNAs in drug resistance for designing novel cancer therapy. Drug Resist Updat 13:57–66PubMedCrossRef Sarkar Fazlul H, Li Yiwei, Wang Zhiwei, Kong Dejuan et al (2010) Implication of microRNAs in drug resistance for designing novel cancer therapy. Drug Resist Updat 13:57–66PubMedCrossRef
19.
Zurück zum Zitat Holleman A, Chung I, Olsen RR, Kwak B, Mizokami A et al (2011) miR-135a contributes to paclitaxel resistance in tumor cells both in vitro and in vivo. Oncogene 30:4386–4398PubMedCrossRef Holleman A, Chung I, Olsen RR, Kwak B, Mizokami A et al (2011) miR-135a contributes to paclitaxel resistance in tumor cells both in vitro and in vivo. Oncogene 30:4386–4398PubMedCrossRef
20.
Zurück zum Zitat Brabletz T (2012) MiR-34 and SNAIL: another double-negative feedback loop controlling cellular plasticity/EMT governed by p53. Cell Cycle 11:215–216PubMedCrossRef Brabletz T (2012) MiR-34 and SNAIL: another double-negative feedback loop controlling cellular plasticity/EMT governed by p53. Cell Cycle 11:215–216PubMedCrossRef
21.
Zurück zum Zitat Cannell IG, Bushell M (2010) Regulation of Myc by miR-34c: a mechanism to prevent genomic instability? Cell Cycle 9:2726–2730PubMedCrossRef Cannell IG, Bushell M (2010) Regulation of Myc by miR-34c: a mechanism to prevent genomic instability? Cell Cycle 9:2726–2730PubMedCrossRef
22.
Zurück zum Zitat Hagman Z, Larne O, Edsjö A, Bjartell A, Ehrnström RA et al (2010) miR-34c is downregulated in prostate cancer and exerts tumor suppressive functions. Int J Cancer 127:2768–2776PubMedCrossRef Hagman Z, Larne O, Edsjö A, Bjartell A, Ehrnström RA et al (2010) miR-34c is downregulated in prostate cancer and exerts tumor suppressive functions. Int J Cancer 127:2768–2776PubMedCrossRef
23.
Zurück zum Zitat Catuogno S, Cerchia L, Romano G, Pognonec P, Condorelli G et al (2012) miR-34c may protect lung cancer cells from paclitaxel-induced apoptosis. Oncogene 27. doi:10.1038/onc.2012.51 Catuogno S, Cerchia L, Romano G, Pognonec P, Condorelli G et al (2012) miR-34c may protect lung cancer cells from paclitaxel-induced apoptosis. Oncogene 27. doi:10.​1038/​onc.​2012.​51
24.
Zurück zum Zitat Kurbacher CM, Cree IA (2005) Chemosensitivity testing using microplate adenosine triphosphate-based luminescence measurements. Methods Mol Med 110:101–120PubMed Kurbacher CM, Cree IA (2005) Chemosensitivity testing using microplate adenosine triphosphate-based luminescence measurements. Methods Mol Med 110:101–120PubMed
25.
Zurück zum Zitat Benes V, Castoldi M (2010) Expression profiling of microRNA using real-time quantitative PCR, how to use it and what is available. Methods 50:244–249PubMedCrossRef Benes V, Castoldi M (2010) Expression profiling of microRNA using real-time quantitative PCR, how to use it and what is available. Methods 50:244–249PubMedCrossRef
26.
Zurück zum Zitat Witkos TM, Koscianska E, Krzyzosiak WJ (2011) Practical aspects of microRNA target prediction. Curr Mol Med 11:93–109PubMedCrossRef Witkos TM, Koscianska E, Krzyzosiak WJ (2011) Practical aspects of microRNA target prediction. Curr Mol Med 11:93–109PubMedCrossRef
27.
Zurück zum Zitat Guntur VP, Waldrep JC, Guo JJ, Selting K, Dhand R (2010) Increasing p53 protein sensitizes non-small cell lung cancer to paclitaxel and cisplatin in vitro. Anticancer Res 30:3557–3564PubMed Guntur VP, Waldrep JC, Guo JJ, Selting K, Dhand R (2010) Increasing p53 protein sensitizes non-small cell lung cancer to paclitaxel and cisplatin in vitro. Anticancer Res 30:3557–3564PubMed
28.
Zurück zum Zitat Sharma N, Ramachandran S, Bowers M, Yegappan M, Brown R et al (2000) Multiple factors other than p53 influence colon cancer sensitivity to paclitaxel. Cancer Chemother Pharmacol 46:329–337PubMedCrossRef Sharma N, Ramachandran S, Bowers M, Yegappan M, Brown R et al (2000) Multiple factors other than p53 influence colon cancer sensitivity to paclitaxel. Cancer Chemother Pharmacol 46:329–337PubMedCrossRef
29.
Zurück zum Zitat Ikeda H, Taira N, Hara F, Fujita T, Yamamoto H (2010) The estrogen receptor influences microtubule-associated protein tau (MAPT) expression and the selective estrogen receptor inhibitor fulvestrant downregulates MAPT and increases the sensitivity to taxane in breast cancer cells. Breast Cancer Res 12:R43PubMedCrossRef Ikeda H, Taira N, Hara F, Fujita T, Yamamoto H (2010) The estrogen receptor influences microtubule-associated protein tau (MAPT) expression and the selective estrogen receptor inhibitor fulvestrant downregulates MAPT and increases the sensitivity to taxane in breast cancer cells. Breast Cancer Res 12:R43PubMedCrossRef
30.
Zurück zum Zitat Morris PG, Fornier MN (2008) Microtubule active agents: beyond the taxane frontier. Clin Cancer Res 14:7167–7172PubMedCrossRef Morris PG, Fornier MN (2008) Microtubule active agents: beyond the taxane frontier. Clin Cancer Res 14:7167–7172PubMedCrossRef
31.
Zurück zum Zitat Rouzier R, Rajan R, Wagner P, Hess KR, Gold DL et al (2005) Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci USA 102:8315–8320PubMedCrossRef Rouzier R, Rajan R, Wagner P, Hess KR, Gold DL et al (2005) Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci USA 102:8315–8320PubMedCrossRef
32.
Zurück zum Zitat Yang S, Li Y, Gao J, Zhang T, Li S, Luo A, Chen H, Ding F, Wang X, Liu Z (2012) MicroRNA-34 suppresses breast cancer invasion and metastasis by directly targeting Fra-1. Oncogene doi:10.1038/onc.2012.432 Yang S, Li Y, Gao J, Zhang T, Li S, Luo A, Chen H, Ding F, Wang X, Liu Z (2012) MicroRNA-34 suppresses breast cancer invasion and metastasis by directly targeting Fra-1. Oncogene doi:10.​1038/​onc.​2012.​432
33.
Zurück zum Zitat He C, Xiong J, Xu X, Lu W, Liu L (2009) Functional elucidation of MiR-34 in osteosarcoma cells and primary tumor samples. Biochem Biophys Res Commun 388:35–40PubMedCrossRef He C, Xiong J, Xu X, Lu W, Liu L (2009) Functional elucidation of MiR-34 in osteosarcoma cells and primary tumor samples. Biochem Biophys Res Commun 388:35–40PubMedCrossRef
34.
Zurück zum Zitat Agirre X, Martínez-Climent JA, Odero MD, Prósper F (2012) Epigenetic regulation of miRNA genes in acute leukemia. Leukemia 26:395–403PubMedCrossRef Agirre X, Martínez-Climent JA, Odero MD, Prósper F (2012) Epigenetic regulation of miRNA genes in acute leukemia. Leukemia 26:395–403PubMedCrossRef
35.
Zurück zum Zitat Hata A, Davis BN (2011) Regulation of pri-miRNA processing through Smads. Adv Exp Med Biol 700:15–27PubMedCrossRef Hata A, Davis BN (2011) Regulation of pri-miRNA processing through Smads. Adv Exp Med Biol 700:15–27PubMedCrossRef
36.
Zurück zum Zitat Kim NH, Kim HS, Kim NG, Lee I, Choi HS (2011) p53 and microRNA-34 are suppressors of canonical Wnt signaling. Sci Signal. 4:ra71PubMedCrossRef Kim NH, Kim HS, Kim NG, Lee I, Choi HS (2011) p53 and microRNA-34 are suppressors of canonical Wnt signaling. Sci Signal. 4:ra71PubMedCrossRef
37.
Zurück zum Zitat Wong MY, Yu Y, Walsh WR, Yang JL (2011) microRNA-34 family and treatment of cancers with mutant or wild-type p53. Int J Oncol 38:1189–1195PubMedCrossRef Wong MY, Yu Y, Walsh WR, Yang JL (2011) microRNA-34 family and treatment of cancers with mutant or wild-type p53. Int J Oncol 38:1189–1195PubMedCrossRef
38.
Zurück zum Zitat Kubo T, Toyooka S, Tsukuda K, Sakaguchi M, Fukazawa T et al (2011) Epigenetic silencing of microRNA-34b/c plays an important role in the pathogenesis of malignant pleural mesothelioma. Clin Cancer Res 17:4965–4974PubMedCrossRef Kubo T, Toyooka S, Tsukuda K, Sakaguchi M, Fukazawa T et al (2011) Epigenetic silencing of microRNA-34b/c plays an important role in the pathogenesis of malignant pleural mesothelioma. Clin Cancer Res 17:4965–4974PubMedCrossRef
Metadaten
Titel
Regulation of microtubule-associated protein tau (MAPT) by miR-34c-5p determines the chemosensitivity of gastric cancer to paclitaxel
verfasst von
Hao Wu
Min Huang
Mingjie Lu
Wei Zhu
Yongqian Shu
Peng Cao
Ping Liu
Publikationsdatum
01.05.2013
Verlag
Springer-Verlag
Erschienen in
Cancer Chemotherapy and Pharmacology / Ausgabe 5/2013
Print ISSN: 0344-5704
Elektronische ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-013-2108-y

Weitere Artikel der Ausgabe 5/2013

Cancer Chemotherapy and Pharmacology 5/2013 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

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