Skip to main content
Erschienen in: Cellular Oncology 5/2017

20.06.2017 | Report

Changes in plasma miR-9, miR-16, miR-205 and miR-486 levels after non-small cell lung cancer resection

verfasst von: Maria Sromek, Maciej Glogowski, Magdalena Chechlinska, Mariusz Kulinczak, Lukasz Szafron, Klara Zakrzewska, Joanna Owczarek, Piotr Wisniewski, Robert Wlodarczyk, Lukasz Talarek, Maciej Turski, Jan Konrad Siwicki

Erschienen in: Cellular Oncology | Ausgabe 5/2017

Einloggen, um Zugang zu erhalten

Abstract

Purpose

The majority of non-small cell lung cancer (NSCLC) patients presents with an advanced-stage disease and, consequently, exhibits a poor overall survival rate. We aimed to assess changes in plasma miR-9, miR-16, miR-205 and miR-486 levels and their potential as biomarkers for the diagnosis and monitoring of NSCLC patients.

Methods

Plasma was collected from 50 healthy donors and from NSCLC patients before surgery (n = 61), 1 month after surgery (n = 37) and 1 year after surgery (n = 14). microRNA levels were quantified using qRT-PCR.

Results

We found in NSCLC patients before treatment, both with squamous cell carcinoma (SQCC) and adenocarcinoma (ADC), significantly higher plasma miR-16 and miR-486 levels than in healthy individuals. Pre-treatment miR-205 concentrations were found to be significantly higher in SQCC than in ADC patients, and only SQCC patients presented significantly higher circulating miR-205 levels than healthy donors. SQCC plasma miR-9 levels were not different from normal control levels, but in ADC they were found to be significantly decreased. A combination of plasma miR-16, miR-205 and miR-486 measurements was found to discriminate NSCLC patients from healthy persons, with a specificity of 95% and a sensitivity of 80%. Following tumor resection, we found that the miR-9 and miR-205 levels significantly decreased, even below the normal level, whereas the increased miR-486 level persisted up to one year after surgery, and the miR-16 level decreased to normal. After tumor resection, none of the miR levels tested was found to relate to recurrence.

Conclusions

Our data indicate that miR-9, miR-16, miR-205 and miR-486 may serve as NSCLC biomarkers. The observed cancer-related pre- and post-operative changes in their plasma levels may not only reflect the presence of a primary cancer, but also of a systemic response to cancer.
Literatur
1.
Zurück zum Zitat S.D. Alipoor, I.M. Adcock, J. Garssen, E. Mortaz, M. Varahram, M. Mirsaeidi, A. Velayati, The roles of miRNAs as potential biomarkers in lung diseases. Eur. J. Pharmacol. 791, 395–404 (2016)CrossRefPubMed S.D. Alipoor, I.M. Adcock, J. Garssen, E. Mortaz, M. Varahram, M. Mirsaeidi, A. Velayati, The roles of miRNAs as potential biomarkers in lung diseases. Eur. J. Pharmacol. 791, 395–404 (2016)CrossRefPubMed
2.
Zurück zum Zitat E. Prodromaki, A. Korpetinou, E. Giannopoulou, E. Vlotinou, M. Chatziathanasiadou, N.I. Papachristou, C.D. Scopa, H. Papadaki, H.P. Kalofonos, D.J. Papachristou, Expression of the microRNA regulators Drosha, dicer and Ago2 in non-small cell lung carcinomas. Cell. Oncol. 38, 307–317 (2015)CrossRef E. Prodromaki, A. Korpetinou, E. Giannopoulou, E. Vlotinou, M. Chatziathanasiadou, N.I. Papachristou, C.D. Scopa, H. Papadaki, H.P. Kalofonos, D.J. Papachristou, Expression of the microRNA regulators Drosha, dicer and Ago2 in non-small cell lung carcinomas. Cell. Oncol. 38, 307–317 (2015)CrossRef
3.
Zurück zum Zitat D. Li, D.Q. Li, D. Liu, X.J. Tang, MiR-613 induces cell cycle arrest by targeting CDK4 in non-small cell lung cancer. Cell. Oncol. 39, 139–147 (2016)CrossRef D. Li, D.Q. Li, D. Liu, X.J. Tang, MiR-613 induces cell cycle arrest by targeting CDK4 in non-small cell lung cancer. Cell. Oncol. 39, 139–147 (2016)CrossRef
4.
Zurück zum Zitat N. Bandi, S. Zbinden, M. Gugger, M. Arnold, V. Kocher, L. Hasan, A. Kappeler, T. Brunner, E. Vassella, miR-15a and miR-16 are implicated in cell cycle regulation in a Rb-dependent manner and are frequently deleted or down-regulated in non-small cell lung cancer. Cancer Res. 69, 5553–5559 (2009)CrossRefPubMed N. Bandi, S. Zbinden, M. Gugger, M. Arnold, V. Kocher, L. Hasan, A. Kappeler, T. Brunner, E. Vassella, miR-15a and miR-16 are implicated in cell cycle regulation in a Rb-dependent manner and are frequently deleted or down-regulated in non-small cell lung cancer. Cancer Res. 69, 5553–5559 (2009)CrossRefPubMed
5.
Zurück zum Zitat A. Navarro, T. Diaz, E. Gallardo, N. Vinolas, R.M. Marrades, B. Gel, M. Campayo, A. Quera, E. Bandres, J. Garcia-Foncillas, J. Ramirez, M. Monzo, Prognostic implications of miR-16 expression levels in resected non-small-cell lung cancer. J. Surg. Oncol. 103, 411–415 (2011)CrossRefPubMed A. Navarro, T. Diaz, E. Gallardo, N. Vinolas, R.M. Marrades, B. Gel, M. Campayo, A. Quera, E. Bandres, J. Garcia-Foncillas, J. Ramirez, M. Monzo, Prognostic implications of miR-16 expression levels in resected non-small-cell lung cancer. J. Surg. Oncol. 103, 411–415 (2011)CrossRefPubMed
6.
Zurück zum Zitat Y. Ke, W. Zhao, J. Xiong, R. Cao, Downregulation of miR-16 promotes growth and motility by targeting HDGF in non-small cell lung cancer cells. FEBS Lett. 587, 3153–3157 (2013)CrossRefPubMed Y. Ke, W. Zhao, J. Xiong, R. Cao, Downregulation of miR-16 promotes growth and motility by targeting HDGF in non-small cell lung cancer cells. FEBS Lett. 587, 3153–3157 (2013)CrossRefPubMed
7.
Zurück zum Zitat M. Crawford, K. Batte, L. Yu, X. Wu, G.J. Nuovo, C.B. Marsh, G.A. Otterson, S.P. Nana-Sinkam, MicroRNA 133B targets pro-survival molecules MCL-1 and BCL2L2 in lung cancer. Biochem. Biophys. Res. Commun. 388, 483–489 (2009)CrossRefPubMedPubMedCentral M. Crawford, K. Batte, L. Yu, X. Wu, G.J. Nuovo, C.B. Marsh, G.A. Otterson, S.P. Nana-Sinkam, MicroRNA 133B targets pro-survival molecules MCL-1 and BCL2L2 in lung cancer. Biochem. Biophys. Res. Commun. 388, 483–489 (2009)CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat U. Vosa, T. Vooder, R. Kolde, K. Fischer, K. Valk, N. Tonisson, R. Roosipuu, J. Vilo, A. Metspalu, T. Annilo, Identification of miR-374a as a prognostic marker for survival in patients with early-stage nonsmall cell lung cancer. Genes Chromosom. Cancer 50, 812–822 (2011)CrossRefPubMed U. Vosa, T. Vooder, R. Kolde, K. Fischer, K. Valk, N. Tonisson, R. Roosipuu, J. Vilo, A. Metspalu, T. Annilo, Identification of miR-374a as a prognostic marker for survival in patients with early-stage nonsmall cell lung cancer. Genes Chromosom. Cancer 50, 812–822 (2011)CrossRefPubMed
9.
Zurück zum Zitat J. Ma, K. Mannoor, L. Gao, A. Tan, M.A. Guarnera, M. Zhan, A. Shetty, S.A. Stass, L. Xing, F. Jiang, Characterization of microRNA transcriptome in lung cancer by next-generation deep sequencing. Mol. Oncol. 8, 1208–1219 (2014)CrossRefPubMedPubMedCentral J. Ma, K. Mannoor, L. Gao, A. Tan, M.A. Guarnera, M. Zhan, A. Shetty, S.A. Stass, L. Xing, F. Jiang, Characterization of microRNA transcriptome in lung cancer by next-generation deep sequencing. Mol. Oncol. 8, 1208–1219 (2014)CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat R. Mitra, M.D. Edmonds, J. Sun, M. Zhao, H. Yu, C.M. Eischen, Z. Zhao, Reproducible combinatorial regulatory networks elucidate novel oncogenic microRNAs in non-small cell lung cancer. RNA 20, 1356–1368 (2014)CrossRefPubMedPubMedCentral R. Mitra, M.D. Edmonds, J. Sun, M. Zhao, H. Yu, C.M. Eischen, Z. Zhao, Reproducible combinatorial regulatory networks elucidate novel oncogenic microRNAs in non-small cell lung cancer. RNA 20, 1356–1368 (2014)CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Y. Peng, Y. Dai, C. Hitchcock, X. Yang, E.S. Kassis, L. Liu, Z. Luo, H.L. Sun, R. Cui, H. Wei, T. Kim, T.J. Lee, Y.J. Jeon, G.J. Nuovo, S. Volinia, Q. He, J. Yu, P. Nana-Sinkam, C.M. Croce, Insulin growth factor signaling is regulated by microRNA-486, an underexpressed microRNA in lung cancer. Proc. Natl. Acad. Sci. U. S. A. 110, 15043–15048 (2013)CrossRefPubMedPubMedCentral Y. Peng, Y. Dai, C. Hitchcock, X. Yang, E.S. Kassis, L. Liu, Z. Luo, H.L. Sun, R. Cui, H. Wei, T. Kim, T.J. Lee, Y.J. Jeon, G.J. Nuovo, S. Volinia, Q. He, J. Yu, P. Nana-Sinkam, C.M. Croce, Insulin growth factor signaling is regulated by microRNA-486, an underexpressed microRNA in lung cancer. Proc. Natl. Acad. Sci. U. S. A. 110, 15043–15048 (2013)CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat M. Boeri, C. Verri, D. Conte, L. Roz, P. Modena, F. Facchinetti, E. Calabro, C.M. Croce, U. Pastorino, G. Sozzi, MicroRNA signatures in tissues and plasma predict development and prognosis of computed tomography detected lung cancer. Proc. Natl. Acad. Sci. U. S. A. 108, 3713–3718 (2011)CrossRefPubMedPubMedCentral M. Boeri, C. Verri, D. Conte, L. Roz, P. Modena, F. Facchinetti, E. Calabro, C.M. Croce, U. Pastorino, G. Sozzi, MicroRNA signatures in tissues and plasma predict development and prognosis of computed tomography detected lung cancer. Proc. Natl. Acad. Sci. U. S. A. 108, 3713–3718 (2011)CrossRefPubMedPubMedCentral
13.
Zurück zum Zitat C.C. Solomides, B.J. Evans, J.M. Navenot, R. Vadigepalli, S.C. Peiper, Z.X. Wang, MicroRNA profiling in lung cancer reveals new molecular markers for diagnosis. Acta Cytol. 56, 645–654 (2012)CrossRefPubMed C.C. Solomides, B.J. Evans, J.M. Navenot, R. Vadigepalli, S.C. Peiper, Z.X. Wang, MicroRNA profiling in lung cancer reveals new molecular markers for diagnosis. Acta Cytol. 56, 645–654 (2012)CrossRefPubMed
14.
Zurück zum Zitat Y. Shao, Y.Q. Shen, Y.L. Li, C. Liang, B.J. Zhang, S.D. Lu, Y.Y. He, P. Wang, Q.L. Sun, Y.X. Jin, Z.L. Ma, Direct repression of the oncogene CDK4 by the tumor suppressor miR-486-5p in non-small cell lung cancer. Oncotarget 7, 34011–34021 (2016)CrossRefPubMedPubMedCentral Y. Shao, Y.Q. Shen, Y.L. Li, C. Liang, B.J. Zhang, S.D. Lu, Y.Y. He, P. Wang, Q.L. Sun, Y.X. Jin, Z.L. Ma, Direct repression of the oncogene CDK4 by the tumor suppressor miR-486-5p in non-small cell lung cancer. Oncotarget 7, 34011–34021 (2016)CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat D. Lebanony, H. Benjamin, S. Gilad, M. Ezagouri, A. Dov, K. Ashkenazi, N. Gefen, S. Izraeli, G. Rechavi, H. Pass, D. Nonaka, J. Li, Y. Spector, N. Rosenfeld, A. Chajut, D. Cohen, R. Aharonov, M. Mansukhani, Diagnostic assay based on hsa-miR-205 expression distinguishes squamous from nonsquamous non-small-cell lung carcinoma. J. Clin. Oncol. 27, 2030–2037 (2009)CrossRefPubMed D. Lebanony, H. Benjamin, S. Gilad, M. Ezagouri, A. Dov, K. Ashkenazi, N. Gefen, S. Izraeli, G. Rechavi, H. Pass, D. Nonaka, J. Li, Y. Spector, N. Rosenfeld, A. Chajut, D. Cohen, R. Aharonov, M. Mansukhani, Diagnostic assay based on hsa-miR-205 expression distinguishes squamous from nonsquamous non-small-cell lung carcinoma. J. Clin. Oncol. 27, 2030–2037 (2009)CrossRefPubMed
16.
Zurück zum Zitat J. Hamamoto, K. Soejima, S. Yoda, K. Naoki, S. Nakayama, R. Satomi, H. Terai, S. Ikemura, T. Sato, H. Yasuda, Y. Hayashi, M. Sakamoto, T. Takebayashi, T. Betsuyaku, Identification of microRNAs differentially expressed between lung squamous cell carcinoma and lung adenocarcinoma. Mol. Med. Rep. 8, 456–462 (2013)CrossRefPubMed J. Hamamoto, K. Soejima, S. Yoda, K. Naoki, S. Nakayama, R. Satomi, H. Terai, S. Ikemura, T. Sato, H. Yasuda, Y. Hayashi, M. Sakamoto, T. Takebayashi, T. Betsuyaku, Identification of microRNAs differentially expressed between lung squamous cell carcinoma and lung adenocarcinoma. Mol. Med. Rep. 8, 456–462 (2013)CrossRefPubMed
17.
Zurück zum Zitat A. Fassina, R. Cappellesso, M. Fassan, Classification of non-small cell lung carcinoma in transthoracic needle specimens using microRNA expression profiling. Chest 140, 1305–1311 (2011)CrossRefPubMed A. Fassina, R. Cappellesso, M. Fassan, Classification of non-small cell lung carcinoma in transthoracic needle specimens using microRNA expression profiling. Chest 140, 1305–1311 (2011)CrossRefPubMed
18.
Zurück zum Zitat L.M. Sholl, D.L. Aisner, T.C. Allen, M.B. Beasley, P.T. Cagle, V.L. Capelozzi, S. Dacic, L.P. Hariri, K.M. Kerr, S. Lantuejoul, M. Mino-Kenudson, K. Raparia, N. Rekhtman, S. Roy-Chowdhuri, E. Thunnissen, M. Tsao, M. Vivero, Y. Yatabe, Liquid biopsy in lung ancer: a perspective from members of the pulmonary pathology society. Arch. Pathol. Lab. Med. 140, 825–829 (2016)CrossRefPubMed L.M. Sholl, D.L. Aisner, T.C. Allen, M.B. Beasley, P.T. Cagle, V.L. Capelozzi, S. Dacic, L.P. Hariri, K.M. Kerr, S. Lantuejoul, M. Mino-Kenudson, K. Raparia, N. Rekhtman, S. Roy-Chowdhuri, E. Thunnissen, M. Tsao, M. Vivero, Y. Yatabe, Liquid biopsy in lung ancer: a perspective from members of the pulmonary pathology society. Arch. Pathol. Lab. Med. 140, 825–829 (2016)CrossRefPubMed
19.
Zurück zum Zitat V.N. Aushev, I.B. Zborovskaya, K.K. Laktionov, N. Girard, M.P. Cros, Z. Herceg, V. Krutovskikh, Comparisons of microRNA patterns in plasma before and after tumor removal reveal new biomarkers of lung squamous cell carcinoma. PLoS One 8, e78649 (2013)CrossRefPubMedPubMedCentral V.N. Aushev, I.B. Zborovskaya, K.K. Laktionov, N. Girard, M.P. Cros, Z. Herceg, V. Krutovskikh, Comparisons of microRNA patterns in plasma before and after tumor removal reveal new biomarkers of lung squamous cell carcinoma. PLoS One 8, e78649 (2013)CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat E. Brambilla, W.D. Travis, A.P. Burke, A. Marx, A.G. Nicholson, WHO classification of tumours of the lung, pleura, thymus and heart (International Agency for Research on Cancer 2015, Lyon) E. Brambilla, W.D. Travis, A.P. Burke, A. Marx, A.G. Nicholson, WHO classification of tumours of the lung, pleura, thymus and heart (International Agency for Research on Cancer 2015, Lyon)
21.
22.
Zurück zum Zitat W. Li, Y. Wang, Q. Zhang, L. Tang, X. Liu, Y. Dai, L. Xiao, S. Huang, L. Chen, Z. Guo, J. Lu, K. Yuan, MicroRNA-486 as a biomarker for early diagnosis and recurrence of non-small cell lung cancer. PLoS One 10, e0134220 (2015)CrossRefPubMedPubMedCentral W. Li, Y. Wang, Q. Zhang, L. Tang, X. Liu, Y. Dai, L. Xiao, S. Huang, L. Chen, Z. Guo, J. Lu, K. Yuan, MicroRNA-486 as a biomarker for early diagnosis and recurrence of non-small cell lung cancer. PLoS One 10, e0134220 (2015)CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat X. Wang, X. Zhi, Y. Zhang, G. An, G. Feng, Role of plasma MicroRNAs in the early diagnosis of non-small-cell lung cancers: a case-control study. J. Thorac. Dis. 8, 1645–1652 (2016)CrossRefPubMedPubMedCentral X. Wang, X. Zhi, Y. Zhang, G. An, G. Feng, Role of plasma MicroRNAs in the early diagnosis of non-small-cell lung cancers: a case-control study. J. Thorac. Dis. 8, 1645–1652 (2016)CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat P. Mozzoni, I. Banda, M. Goldoni, M. Corradi, M. Tiseo, O. Acampa, V. Balestra, L. Ampollini, A. Casalini, P. Carbognani, A. Mutti, Plasma and EBC microRNAs as early biomarkers of non-small-cell lung cancer. Biomarkers 18, 679–686 (2013)CrossRefPubMed P. Mozzoni, I. Banda, M. Goldoni, M. Corradi, M. Tiseo, O. Acampa, V. Balestra, L. Ampollini, A. Casalini, P. Carbognani, A. Mutti, Plasma and EBC microRNAs as early biomarkers of non-small-cell lung cancer. Biomarkers 18, 679–686 (2013)CrossRefPubMed
26.
Zurück zum Zitat W. Wang, M. Corrigan-Cummins, E.A. Barber, L.M. Saleh, A. Zingone, A. Ghafoor, R. Costello, Y. Zhang, R.J. Kurlander, N. Korde, A.M. Roccaro, I.M. Ghobrial, O. Landgren, K.R. Calvo, Aberrant levels of miRNAs in bone marrow microenvironment and peripheral blood of myeloma patients and disease progression. J. Mol. Diagn. 17, 669–678 (2015)CrossRefPubMedPubMedCentral W. Wang, M. Corrigan-Cummins, E.A. Barber, L.M. Saleh, A. Zingone, A. Ghafoor, R. Costello, Y. Zhang, R.J. Kurlander, N. Korde, A.M. Roccaro, I.M. Ghobrial, O. Landgren, K.R. Calvo, Aberrant levels of miRNAs in bone marrow microenvironment and peripheral blood of myeloma patients and disease progression. J. Mol. Diagn. 17, 669–678 (2015)CrossRefPubMedPubMedCentral
27.
Zurück zum Zitat V.J. Cookson, M.A. Bentley, B.V. Hogan, K. Horgan, B.E. Hayward, L.D. Hazelwood, T.A. Hughes, Circulating microRNA profiles reflect the presence of breast tumours but not the profiles of microRNAs within the tumours. Cell. Oncol. 35, 301–308 (2012)CrossRef V.J. Cookson, M.A. Bentley, B.V. Hogan, K. Horgan, B.E. Hayward, L.D. Hazelwood, T.A. Hughes, Circulating microRNA profiles reflect the presence of breast tumours but not the profiles of microRNAs within the tumours. Cell. Oncol. 35, 301–308 (2012)CrossRef
28.
Zurück zum Zitat R.P. Panganiban, Y. Wang, J. Howrylak, V.M. Chinchilli, T.J. Craig, A. August, F.T. Ishmael, Circulating microRNAs as biomarkers in patients with allergic rhinitis and asthma. J. Allergy Clin. Immunol. 137, 1423–1432 (2016)CrossRefPubMed R.P. Panganiban, Y. Wang, J. Howrylak, V.M. Chinchilli, T.J. Craig, A. August, F.T. Ishmael, Circulating microRNAs as biomarkers in patients with allergic rhinitis and asthma. J. Allergy Clin. Immunol. 137, 1423–1432 (2016)CrossRefPubMed
29.
Zurück zum Zitat A. Warth, T. Muley, E. Herpel, M. Meister, F.J. Herth, P. Schirmacher, W. Weichert, H. Hoffmann, P.A. Schnabel, Large-scale comparative analyses of immunomarkers for diagnostic subtyping of non-small-cell lung cancer biopsies. Histopathology 61, 1017–1025 (2012)CrossRefPubMed A. Warth, T. Muley, E. Herpel, M. Meister, F.J. Herth, P. Schirmacher, W. Weichert, H. Hoffmann, P.A. Schnabel, Large-scale comparative analyses of immunomarkers for diagnostic subtyping of non-small-cell lung cancer biopsies. Histopathology 61, 1017–1025 (2012)CrossRefPubMed
30.
Zurück zum Zitat A.V. Kossenkov, A. Vachani, C. Chang, C. Nichols, S. Billouin, W. Horng, W.N. Rom, S.M. Albelda, M.K. Showe, L.C. Showe, Resection of non-small cell lung cancers reverses tumor-induced gene expression changes in the peripheral immune system. Clin. Cancer Res. 17, 5867–5877 (2011)CrossRefPubMedPubMedCentral A.V. Kossenkov, A. Vachani, C. Chang, C. Nichols, S. Billouin, W. Horng, W.N. Rom, S.M. Albelda, M.K. Showe, L.C. Showe, Resection of non-small cell lung cancers reverses tumor-induced gene expression changes in the peripheral immune system. Clin. Cancer Res. 17, 5867–5877 (2011)CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat D. Subotic, D. Mandaric, G. Radosavljevic, J. Stojsic, M. Gajic, Lung function changes and complications after lobectomy for lung cancer in septuagenarians. Ann. Thorac. Med. 4, 54–59 (2009)CrossRefPubMedPubMedCentral D. Subotic, D. Mandaric, G. Radosavljevic, J. Stojsic, M. Gajic, Lung function changes and complications after lobectomy for lung cancer in septuagenarians. Ann. Thorac. Med. 4, 54–59 (2009)CrossRefPubMedPubMedCentral
32.
Zurück zum Zitat C.G. Xu, M.F. Yang, J.X. Fan, W. Wang, MiR-30a and miR-205 are downregulated in hypoxia and modulate radiosensitivity of prostate cancer cells by inhibiting autophagy via TP53INP1. Eur. Rev. Med. Pharmacol. Sci. 20, 1501–1508 (2016)PubMed C.G. Xu, M.F. Yang, J.X. Fan, W. Wang, MiR-30a and miR-205 are downregulated in hypoxia and modulate radiosensitivity of prostate cancer cells by inhibiting autophagy via TP53INP1. Eur. Rev. Med. Pharmacol. Sci. 20, 1501–1508 (2016)PubMed
33.
Zurück zum Zitat X.F. Shi, H. Wang, F.J. Xiao, Y. Yin, Q.Q. Xu, R.L. Ge, L.S. Wang, MiRNA-486 regulates angiogenic activity and survival of mesenchymal stem cells under hypoxia through modulating Akt signal. Biochem. Biophys. Res. Commun. 470, 670–677 (2016)CrossRefPubMed X.F. Shi, H. Wang, F.J. Xiao, Y. Yin, Q.Q. Xu, R.L. Ge, L.S. Wang, MiRNA-486 regulates angiogenic activity and survival of mesenchymal stem cells under hypoxia through modulating Akt signal. Biochem. Biophys. Res. Commun. 470, 670–677 (2016)CrossRefPubMed
35.
Zurück zum Zitat H. Konishi, D. Ichikawa, S. Komatsu, A. Shiozaki, M. Tsujiura, H. Takeshita, R. Morimura, H. Nagata, T. Arita, T. Kawaguchi, S. Hirashima, H. Fujiwara, K. Okamoto, E. Otsuji, Detection of gastric cancer-associated microRNAs on microRNA microarray comparing pre- and post-operative plasma. Br. J. Cancer 106, 740–747 (2012)CrossRefPubMedPubMedCentral H. Konishi, D. Ichikawa, S. Komatsu, A. Shiozaki, M. Tsujiura, H. Takeshita, R. Morimura, H. Nagata, T. Arita, T. Kawaguchi, S. Hirashima, H. Fujiwara, K. Okamoto, E. Otsuji, Detection of gastric cancer-associated microRNAs on microRNA microarray comparing pre- and post-operative plasma. Br. J. Cancer 106, 740–747 (2012)CrossRefPubMedPubMedCentral
36.
Zurück zum Zitat X. Chen, L. Zhu, Z. Ma, G. Sun, X. Luo, M. Li, S. Zhai, P. Li, X. Wang, Oncogenic miR-9 is a target of erlotinib in NSCLCs. Sci. Report. 5, 17031 (2015)CrossRef X. Chen, L. Zhu, Z. Ma, G. Sun, X. Luo, M. Li, S. Zhai, P. Li, X. Wang, Oncogenic miR-9 is a target of erlotinib in NSCLCs. Sci. Report. 5, 17031 (2015)CrossRef
37.
Zurück zum Zitat G. Chen, J. Wang, Q. Cui, Could circulating miRNAs contribute to cancer therapy? Trends Mol. Med. 19, 71–73 (2013)CrossRefPubMed G. Chen, J. Wang, Q. Cui, Could circulating miRNAs contribute to cancer therapy? Trends Mol. Med. 19, 71–73 (2013)CrossRefPubMed
38.
Zurück zum Zitat K.W. Witwer, Circulating microRNA biomarker studies: pitfalls and potential solutions. Clin. Chem. 61, 56–63 (2015)CrossRefPubMed K.W. Witwer, Circulating microRNA biomarker studies: pitfalls and potential solutions. Clin. Chem. 61, 56–63 (2015)CrossRefPubMed
Metadaten
Titel
Changes in plasma miR-9, miR-16, miR-205 and miR-486 levels after non-small cell lung cancer resection
verfasst von
Maria Sromek
Maciej Glogowski
Magdalena Chechlinska
Mariusz Kulinczak
Lukasz Szafron
Klara Zakrzewska
Joanna Owczarek
Piotr Wisniewski
Robert Wlodarczyk
Lukasz Talarek
Maciej Turski
Jan Konrad Siwicki
Publikationsdatum
20.06.2017
Verlag
Springer Netherlands
Erschienen in
Cellular Oncology / Ausgabe 5/2017
Print ISSN: 2211-3428
Elektronische ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-017-0334-8

Weitere Artikel der Ausgabe 5/2017

Cellular Oncology 5/2017 Zur Ausgabe

Neu im Fachgebiet Pathologie

Molekularpathologische Untersuchungen im Wandel der Zeit

Open Access Biomarker Leitthema

Um auch an kleinen Gewebeproben zuverlässige und reproduzierbare Ergebnisse zu gewährleisten ist eine strenge Qualitätskontrolle in jedem Schritt des Arbeitsablaufs erforderlich. Eine nicht ordnungsgemäße Prüfung oder Behandlung des …

Vergleichende Pathologie in der onkologischen Forschung

Pathologie Leitthema

Die vergleichende experimentelle Pathologie („comparative experimental pathology“) ist ein Fachbereich an der Schnittstelle von Human- und Veterinärmedizin. Sie widmet sich der vergleichenden Erforschung von Gemeinsamkeiten und Unterschieden von …

Gastrointestinale Stromatumoren

Open Access GIST CME-Artikel

Gastrointestinale Stromatumoren (GIST) stellen seit über 20 Jahren ein Paradigma für die zielgerichtete Therapie mit Tyrosinkinaseinhibitoren dar. Eine elementare Voraussetzung für eine mögliche neoadjuvante oder adjuvante Behandlung bei …

Personalisierte Medizin in der Onkologie

Aufgrund des erheblichen technologischen Fortschritts in der molekularen und genetischen Diagnostik sowie zunehmender Erkenntnisse über die molekulare Pathogenese von Krankheiten hat in den letzten zwei Jahrzehnten ein grundlegender …