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Role of cancer stem cells and microRNA in resistance to chemotherapy in patients with ovarian cancer

  • A. Markowska1,*,
  • S. Sajdak2

1Department of Perinatology and Gynecology, Poznan University of Medical Sciences, Poznan, Poland

2Department of Gynecological Surgery, Poznan University of Medical Sciences, Poznan, Poland

DOI: 10.12892/ejgo3412.2017 Vol.38,Issue 2,April 2017 pp.181-183

Published: 10 April 2017

*Corresponding Author(s): A. Markowska E-mail: nnamarkowska@vp.pl

Abstract

Despite the introduction of “the golden standard” in chemotherapy for ovarian cancer (taxanes/platinum), a relapse of the disease is noted in 80% of women treated in this manner. Studies on ovarian cancer stem cells (CSCs) and attempts at treatment using salinomycin, isolated from Streptomyces albus and endotoxin of Clostridium perfringens, are promising, in particular because CSC markers have been identified. Resistance of ovarian cancer cells to paclitaxel and cisplatin is associated with a reduced expression of miR-30c, miR-130, and miR335, which results in activation of M-CSF, the known factor of resistance to cytostatic drugs. In clear cell ovarian cancer, a reduced expression of miR-449 was detected, which may lead to overexpression of MET phenotype, typical for chemoresistant ovarian cancer. MicroRNAs remain in investigations, but their involvement in the control of genes linked to the development of the cancer and its progression seems to offer the promise of a targeted therapy.

Keywords

Ovarian cancer; Cancer stem cells; MicroRNA; Resistance to chemotherapy.

Cite and Share

A. Markowska,S. Sajdak. Role of cancer stem cells and microRNA in resistance to chemotherapy in patients with ovarian cancer. European Journal of Gynaecological Oncology. 2017. 38(2);181-183.

References

[1] Niero E.L., Rocha-Sales B., Lauand C., Cortez D.A., de Souze M.M., Rozende-Teixeira P.: “The multiple facets of drug resistance: one history, different approaches”. J. Exp. Clin. Cancer Res., 2014, 33, 37.

[2] Visvader J.E., Lindeman G.J.: “Cancer Stem Cells: Current status and evolving complexities”. Cell Stem Cells, 2012, 10, 717.

[3] Shah M.M., Landen C.N.: “Ovarian cancer stem cells: are they real and why are they important?”. Gynecol. Oncol., 2014, 132, 483.

[4] Klonisch T., Wiechec E., Hombach-Klonisch S., Ande S.R., Wesselborg S., Schulze-Osthoff K., Los M.: “Cancer stem cell markers in common cancers - therapeutic implications”. Trends Mol. Med., 2008, 14, 450.

[5] Massard C., Deutsch E., Soria J.C.: “Tumour stem cell-targeted treatment: elimination or differentiation”. Ann. Oncol., 2006, 17, 1620.

[6] Boesch M., Zeimet A.G., Rumpold H., Gastl G., Sopper S., Wolf D.: “Drug transporter-mediated protection of cancer stem cells from ionophore antibiotics”. Stem Cells Transl. Med., 2015, 4, 1028.

[7] Tomao F., Papa A., Rossi L., Strudel., Vici P., Lo Russo G., Tomao S.: “Emerging role of cancer stem cells in the biology and treatment of ovarian cancer: basic knowledge and therapeutic possibilities for an innovative approach”. J. Exp. Clin. Cancer Res., 2013, 1, 32.

[8] Takebe N., Harris P.J., Warren R.Q., Ivy S.P.: “Targeting cancer stem cells by inhibiting Wnt, Notch, and Hedgehog pathways”. Nat. Rev. Clin. Oncol., 2011, 8, 97.

[9] Zeng J., Ruan J., Luo L., Shi J., Cui Q., Yang J.: “Molecular portraits of heterogeneity related to cancer stem cells in human ovarian cancer”. Int. J. Gynecol. Cancer, 2014, 24, 29.

[10] Abubaker K., Luwor R.B., Escalona R., McNally O., Quinn M.A., Thompson E.W.: “Targeted disruption of the JAK2/STAT3 pathway in combination with systemic administration of paclitaxel inhibits the priming of ovarian cancer stem cells leading to a reduced tumor burden”. Front. Oncol., 2014, 4, 75.

[11] Bapat S.A.: “Focus on stem cells in human reproduction. Human ovarian cancer stem cells”. Reproduction, 2010, 140, 33.

[12] Yu-Zh., Liu T., Zhao YH., Huang Y.Y., Gao Y.T.: “Cisplatin targets the stromal cell-derived factor-1-CXC chemokine receptor type 4 axis to suppress metastasis and invasion of ovarian cancer-initiating cells”. Tumor Biol., 2014, 35, 4637.

[13] Bourguignon L.Y., Peyrollier K., Xia W., Gilad B.: “Hyaluronan-CD44 interaction activates stem cell marker Nanog, Stat-3-mediated MDR1 gene expression, and ankyrin-regulated multidrug efflux in breast and ovarian tumor cells”. J. Biol. Chem., 2008, 283, 17635.

[14] He Q.Z., Luo X.Z., Zhou Q., Wang K., Li S.X., Li Y.: “Expression of nestin in ovarian serous cancer and its clinicopathologic significance”. Eur Rev. Med. Pharmacol. Sci., 2013, 17, 2896.

[15] Craveiro V., Yang-Hartwich Y., Holmberg Je., Pizzonia J., Sumi M.J., Griffin B.: “Phenotypic modifications in ovarian cancer stem cells following paclitaxel treatment”. Cancer Med., 2013, 2, 751.

[16] Prud‘homme G.J.: “Cancer stem cells and novel targets for antitumor strategies”. Curr. Pharm. Des., 2012, 18, 2838

[17] Parajuli B., Shin SJ., Kwon SH., Cha SD., Chung R., Park WJ.: “Salinomycin induces apoptosis via death receptor-5 up-regulation in cisplatin- resistant ovarian cancer cell”. Anticancer Res., 2013, 33(4), 1457.

[18] Casagrande F., Cocco E., Bellone S., Richter C.E., Bellone M., Todeschini P.: “Eradication of chemotherapy-resistant CD44+ human ovarian cancer stem cells in mice by intraperitoneal administration of Clostridium perfringens enterotoxin”. Cancer, 2011, 117, 5519.

[19] Blower P.E., Chung J.H., Verducci J.S., Lin S., Park J.K., Dai Z.: “MicroRNAs modulate the chemosensitivity of tumor cells”. Mol. Cancer Ther., 2008, 7, 1.

[20] Humphries B., Yang C.: “The microRNA-200 family: small molecules with novel roles in cancer development, progression and therapy”. Oncotarget, 2015, 6, 6472.

[21] Feng B., Wang R., Chen LB.: “Review of miR-200b and cancer chemosensivity”. Biomed. Pharmacother., 2012, 66, 397.

[22] Li B., Chen H., Wu N., Zhang W.J., Shang L.X.: “Deregulation of miR-128 in ovarian cancer promotes cisplatin resistance”. Int. J. Gynecol. Cancer, 2014, 24, 1381.

[23] Zong C., Wang J., Shi T.M.: “MicroRNA 130b enhances drug resistance in human ovarian cancer cells”. Tumour Biol., 2014, 35, 12151.

[24] Sorrentino A., Liu C.G., Addario A., Peschle C., Ferlini C.: “Role of microRNAs in drug-resistant ovarian cancer cells”. Gynecol Oncol., 2008, 111(3), 478.

[25] Jang S.G., Yoo C.W., Park S.Y., Kang S., Kim H.K.: “Low expression of miR-449 in gynecologic clear cell carcinoma”. Int. J. Gynecol. Cancer, 2014, 24, 1558.

[26] Haruta S., Furukawa N., Yoshizawa Y., Tsunemi T., Nagai A., Kawaguschi R.: “Molecular genetics and epidemiology of epithelial ovarian cancer (Review)”. Oncol Rep., 2011, 26, 1347.

[27] Weiner-Gorzel K., Dempsey E., Milewska M., McGoldrick A., Toh V., Walsch A.: “Overexpression of the microRNA miR-433 promotes resistance to paclitaxel through the induction of cellular senescence in ovarian cancer cells”. Cancer Med., 2015, 4, 745.

[28] He J., Yu J.J., Xu Q., Wang L., Zheng J.Z., Liu L.Z., Jiang B.M.: “Downregulation of ATG14 by EGR1-MIR152 sensitizes ovarian cancer cells to cisplatin-induced apoptosis by inhibiting cyto-protective autophagy”. Autophagy, 2015, 11, 373.

[29] Mathew R., Withe E.: “Autophagy, stress, and cancer metabolism: what doesn't kill you makes you stronger”. Cold Spring Harb. Symp. Quant. Biol., 2011, 76, 389.

[30] Frisch S.M., Francis H.: “Disruption of epithelial cell-matrix interactions induces apoptosis”. J. Cell. Biol., 1994, 124, 619.

[31] Cittelly D.M., Dimitrova I., Howe E.N., Cochrane D.R., Jean A.: “Restoration of miR-200c to ovarian cancer reduces tumor burden and increases sensitivity to paclitaxel”. Mol Cancer Ther., 2012, 11, 2556

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