|
|
Research progress of miR-200c in thyroid cancer |
ZHANG Yan WU Chenguang |
Department of Endocrinology, People′s Hospital Affiliated to Jiangsu University, Jiangsu Province, Zhenjiang 212002, China |
|
|
Abstract miRNA is a kind of endogenous, non-coding small molecule RNA, which is highly conserved and related to the occurrence and development of various human tumors including thyroid cancer. Compared with differentiated thyroid cancer, the prognosis of undifferentiated thyroid cancer is worse, which may be associated with a higher proportion of cancer stem cells. miR-200c, as a novel tumor suppressor, can inhibit the proliferation of thyroid cancer cells and promote their apoptosis. Moreover, miR-200c can modulate epithelial-mesenchymal transition through transforming growth factor-β (TGF-β) pathway and epidermal growth factor receptor (EGFR) pathway. Recent researches have found that epithelial-mesenchymal transition induces the formation of cancer stem cell. Hence, miR-200c may serve as a potential molecular target for biological treatment of refractory thyroid cancer. The research progress in the relationship between miR-200c and thyroid cancer is reviewed in this paper.
|
|
|
|
|
[1] 董芬,张彪,单广良.中国甲状腺癌的流行现状和影响因素[J].中国癌症杂志,2016,26(1):47-52.
[2] 杨雷,王宁.甲状腺癌流行病学研究进展[J].中华预防医学杂志,2014,48(8):744-748.
[3] 李墨林,贾婷婷,白晗,等.MiRNA与甲状腺癌发生、发展关系的研究进展[J].临床与实验病理学杂志,2015,31(7):794-798.
[4] Li Y,Li S,Zhang Y,et al. Inhibition of papillary thyroid carcinoma growth by miR-200c via suppressing XIAP expression [J]. Inter J Clin Exp Med,2017,10(2):2932-2938.
[5] Feng ZM,Qiu J,Chen XW,et al. Essential role of miR-200c in regulating self-renewal of breast cancer stem cells and their counterparts of mammary epithelium [J]. BMC Cancer,2015,15:645.
[6] Karimi DF,Amini R,Saidijam M,et al. miR-200c,a tumor suppressor that modulate the expression of cancer stem cells markers and epithelial-mesenchymal transition in colorectal cancer [J]. J Cell Biochem,2018,119(7):6288-6295.
[7] Feng X,Wang Z,Fillmore R,et al. MiR-200,a new star miRNA in human cancer [J]. Cancer Lett,2014,344(2):166-173.
[8] Pichler M,Ress AL,Winter E,et al. MiR-200a regulates epithelial to mesenchymal transition-related gene expression and determines prognosis in colorectal cancer patients [J]. Br J Cancer,2014,110(6):1614-1621.
[9] Sulaiman SA,Mutalib NSA,Jamal R. miR-200c Regulation of Metastases in Ovarian Cancer:Potential Role in Epithelial and Mesenchymal Transition [J]. Front Pharmacol,2016,7:271.
[10] Yao Y,Hu J,Shen Z,et al. MiR-200b expression in breast cancer:a prognostic marker and act on cell proliferation and apoptosis by targeting Sp1 [J]. J Cell Mol Med,2015, 19(4):760-769.
[11] Braun J,Hoang VCH,Huttelmaier S. Downregulation of miRNAs directs the EMT and invasive potential of anaplastic thyroid carcinomas [J]. Oncogene,2010,29(29):4237-4244.
[12] Qin Y,Chen W,Liu B,et al. MiR-200c Inhibits the Tumor Progression of Glioma via Targeting Moesin [J]. Theranostics, 2017,7(6):1663-1673.
[13] Petra Obexer MJA. X-Linked Inhibitor of Apoptosis Protein-A Critical Death Resistance Regulator and Therapeutic Target for Personalized Cancer Therapy [J]. Front Oncol,2014,4:197.
[14] Xue L,Su D,Li D,et al. miR-200 Regulates Epithelial-Mesenchymal Transition in Anaplastic Thyroid Cancer via EGF/EGFR Signaling [J]. Cell Biochem Biophys,2013,24(2):85-91.
[15] Sundararajan V,Gengenbacher N,Stemmler MP,et al. The ZEB1/miR-200c feedback loop regulates invasion via actin interacting proteins MYLK and TKS5 [J]. Oncotarget,2015,6(29):27 083-27 096.
[16] Fang Y,Yu S,Braley-Mullen H. TGF-β Promotes Proliferation of Thyroid Epithelial Cells in IFN-γ-/- Mice by Down-Regulation of p21 and p27 via AKT Pathway [J]. Am J Pathol,2012,180(2):650-660.
[17] Baquero P,Jiménezmora E,Santos A,et al. TGFβ induces epithelial-mesenchymal transition of thyroid cancer cells by both the BRAF/MEK/ERK and Src/FAK pathways [J]. Mol Carcinog,2016,55(11):1639-1654.
[18] Koo T,Cho BJ,Kim DH,et al. MiRNA-200c increases radiosensitivity of human cancer cells with activated EGFR-associated signaling [J]. Oncotarget,2017,8(39):65 457-65 468.
[19] Thiery JP,Acloque H,Huang RY,et al. Epithelial-mesenchymal transitions in development and disease [J]. Cell,2009,139(5);871-890.
[20] Hardin H,Zhang R,Helein H,et al. The evolving concept of cancer stem-like cells in thyroid cancer and other solid tumors [J]. Lab Invest,2017,97(10);1142-1151.
[21] Heiden KB,Williamson AJ,Doscas ME,et al. The sonic hedgehog signaling pathway maintains the cancer stem cell self-renewal of anaplastic thyroid cancer by inducing snail expression [J]. J Clin Endocrinol Metab,2014, 99(11):E2178.
[22] Guo Z,Hardin H,Lloyd RV. Cancer stem-like cells and thyroid cancer [J]. Endocr Relat Cancer,2014,21(5):T285-T300.
[23] Shibue T,Weinberg RA. EMT,CSCs,and drug resistance:the mechanistic link and clinical implications [J]. Nat Rev Clin Oncol,2017,14(10):611-629.
[24] Lan L,Luo Y,Cui D,et al. Epithelial-mesenchymal transition triggers cancer stem cell generation in human thyroid cancer cells [J]. Int J Oncol,2013,43(1):113-120.
[25] 叶丽姿.分化型甲状腺癌的药物治疗进展[J].医学研究生学报,2018,31(5):544-549.
[26] Chen D,Zhang Y,Wang J,et al. MiRNA-200c overexpression inhibits tumorigenicity and metastasis of CD117+CD44+ ovarian cancer stem cells by regulating epithelial-mesenchymal transition [J]. J Ovarian Res,2013,6(1):50.
[27] Jana K,Pfefferle AD,Ivana P,et al. Expression of miR-200c in claudin-low breast cancer alters stem cell functionality,enhances chemosensitivity and reduces metastatic potential [J]. Oncogene,2015,34(49):5997-6006. |
|
|
|