JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES) ›› 2015, Vol. 53 ›› Issue (7): 48-52.doi: 10.6040/j.issn.1671-7554.0.2015.184

Previous Articles     Next Articles

Occurrence of epithelia-mesenchymal transition in endometrial adenocarci-noma and the roles of miR200a/ZEB1 signaling pathway in this process

ZHANG Xiaohui, YAN Lei, QI Shasha, LU Zhenzhen, LI Mingjiang, ZHAO Xingbo   

  1. Department of Obstetrics and Gynecology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, Shandong, China
  • Received:2015-02-13 Revised:2015-04-22 Online:2015-07-10 Published:2015-07-10

Abstract: Objective To investigate the occurrence of epithelia-mesenchymal transition (EMT) in endometrial carcinoma and examine the roles of miR200a/zinc finger E-box-binding protein 1(ZEB1) signaling pathway in this process. Methods Different groups of samples were collected, including paraffin sections of endometrial adenocarcinoma tissues (group A, n=22), endometrial tissues after resection of uterine myoma(group B, n=45), endometrial adenocarcinoma samples obtained during operation(group C, n=15) and healthy endometrial tissues(group D, n=34). Expressions of E-cadherin, Vimentin and ZEB1 in group A and group B were investigated with immunohistochemistry. Expressions of E-cadherin, Vimentin and ZEB1 and their mRNA in group C and group D were evaluated with Western blotting and Real-time RT-PCR. Expression of miR200a in group C and D was determined with Real-time RT-PCR. Results ① Compared with group A, group B had significantly decreased expression of E-cadherin, and markedly increased expressions of Vimentin and ZEB1(both P<0.05). ② Compared with group C, group D had decreased E-cadherin and its mRNA expressions but increased expressions of Vimentin and its mRNA, and ZEB1 and its mRNA (all P<0.05). ③ Compared with group C, group D exhibited remarkably elevated miR200a, which was positively correlated to E-cadherin's mRNA(r=0.63, P<0.01)as indicated by a linear regression analysis. Conclusions EMT occurs in endometrial adenocarcinoma. The miR200/ZEB1signaling pathway can inhibit the important molecular markers in EMT.

Key words: Epithelia-mesenchymal transition, Endometrial andenocarcinoma, Zinc finger E-box-binding protein 1, microRNA200a, Regulation

CLC Number: 

  • R711.74
[1] Azueta A, Gatius S, Matias-Guiu X. Endometrioid carcinoma of the endometrium: pathologic and molecular features[J]. Semin Diagn Pathol, 2010, 27(4):226-240.
[2] Ombrato L, Malanchi I. The EMT universe: space between cancer cell dissemination and metastasis initiation[J]. Crit Rev Oncog, 2014, 19(5):349-361.
[3] Moyret-Lalle C, Ruiz E, Puisieux A. Epithelial-mesenchymal transition transcription factors and miRNAs: “plastic surgeons” of breast cancer[J]. World J Clin Oncol, 2014, 5(3):311-322.
[4] Zhu QC, Gao RY, Wu W, et al. Epithelial-mesenchymal transition and its role in the pathogenesis of colorectal cancer[J]. Asian Pac J Cancer Prev, 2013, 14(5):2689-2698.
[5] Vergara D, Merlot B, Lucot JP, et al. Epithelial-mesenchymal transition in ovarian cancer[J]. Cancer Lett, 2010, 291(1):59-66.
[6] Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015[J]. CA Cancer J Clin, 2015, 65(1):5-29.
[7] Abal M, Llaurado M, Doll A, et al. Molecular determinants of invasion in endometrial cancer[J]. Clin Transl Oncol, 2007, 9(5):272-277.
[8] Giannoni E, Bianchini F, Masieri L, et al. Reciprocal activation of prostate cancer cells and cancer-associated fibroblasts stimulates epithelial-mesenchymal transition and cancer stemness[J]. Cancer Res, 2010, 70(17):6945-6956.
[9] Vella LJ. The emerging role of exosomes in epithelial-mesenchymal-transition in cancer[J]. Front Oncol, 2014, 4:361.
[10] 洪伦. 上皮-间质转化及相关microRNA分子与肿瘤的恶性行为的研究进展[J]. 中国癌症杂志, 2011, 21(9):725-730. HONG Lun. EMT phenomenon and related microRNAs in the malignant progression of tumor[J]. China Oncology, 2011, 21(9):725-730.
[11] Heldin CH, Vanlandewijck M, Moustakas A. Regulation of EMT by TGFbeta in cancer[J]. FEBS Lett, 2012, 586(14):1959-1970.
[12] 刘苹, 李平, 彭艳, 等. 原代成纤维细胞和纤维肉瘤细胞自分泌转化生长因子β1浓度检测及对转化生长因子β1增殖的调节[J]. 中国组织工程研究与临床康复, 2011, 15(41):7669-7672. LIU Ping, LI Ping, PENG Yan, et al. Detection of autocrine transforming growth factor-beta β1 concentration in the primary fibroblasts and fibrosarcoma cells and effects on cell proliferation[J]. Journal of Clinical Rehabilitative Tissue Engineering Research, 2011, 15(41):7669-7672.
[13] Gregory PA, Bracken CP, Smith E, et al. An autocrine TGF-beta/ZEB/miR-200 signaling network regulates establishment and maintenance of epithelial-mesenchymal transition[J]. Mol Biol Cell, 2011, 22(10):1686-1698.
[14] Garofalo M, Croce CM. Role of microRNAs in maintaining cancer stem cells[J]. Adv Drug Deliv Rev, 2015, 81:53-61. doi: 10.1016/j.addr.2014.11.014. Epub 2014 Nov 20.
[15] Korpal M, Kang Y. The emerging role of miR-200 family of microRNAs in epithelial-mesenchymal transition and cancer metastasis[J]. RNA Biol, 2008, 5(3):115-119.
[16] Kinose Y, Sawada K, Nakamura K, et al. The role of microRNAs in ovarian cancer[J]. Biomed Res Int, 2014, 2014: 249393 . doi: 10.1155/2014/249393. Epub 2014 Sep 10.
[17] Li X, Roslan S, Johnstone CN, et al. MiR-200 can repress breast cancer metastasis through ZEB1-independent but moesin-dependent pathways[J]. Oncogene, 2014, 33(31):4077-4088.
[18] Chen Y, Xiao Y, Ge W, et al. miR-200b inhibits TGF-beta1-induced epithelial-mesenchymal transition and promotes growth of intestinal epithelial cells[J]. Cell Death Dis, 2013, 4:e541.doi: 10.1038/cddis.2013.22.
[1] LI Mengmeng, WANG Miaomiao, DIAO Xueqin, TIAN Keli, XU Xia, REN Guijie. Regulatory effect of lncRNA RP11-543N12.1 on the expression of CDH13 in Alzheimers disease cell model [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(3): 12-18.
[2] MENG Fanchao, FENG Lu, SHAO Guangrui. FOXM1 regulates transcription of SYK in breast cancer cell line MCF-7 [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(3): 19-24.
[3] LI Shanshan, YANG Jing, ZHANG Jin. Post-transcriptional regulation mechanism of sclerostin in mice [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2017, 55(3): 43-48.
[4] ZHAO Xiuqin, DENG Chunying, LI Shiying, ZHANG Jinxia, HE Yonggui, YU Hong, LIU Bin. Neuroprotective effect of dl-3n-butylphthalide on focal cerebral ischemia reperfusion injury in rats [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2016, 54(4): 25-31.
[5] LIU Ji-dong, HOU Xin-guo, SONG Jun, LI Wen-juan, XIAO Juan, XIAO Fang,WANG Mei-jian, DENG Nan, ZHOU Xiao-ying, CHEN Li. Cardiovascular risk factors in prehypertensive patients
with impaired glucose regulation
[J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2012, 50(7): 1-.
[6] YU Chun-xiao1,2,3, JIN Tong4, JIANG An-li5, ZHAO Jia-jun1,2,3. Functional analysis in the intron and 10 kb upstream
regions of human homeobox gene NKX3.1
[J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2012, 50(12): 13-.
[7] LI Qiang1,2, CAI Da-xing1, CHEN Guang3, LIU Ji-feng4, LI Chun-yang1. Detection and significance of CD4+CD25+ Foxp3+ regulatory T cells in peripheral blood of patients with vitiligo [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2012, 50(1): 133-.
[8] CHEN Jie1, SONG Yong-hong2, WANG Shu-rong2, HAN Zhen-long3, JIANG Xue-bing1, LI Guo-sheng1, GUO Chun1, ZHANG Li-ning1, SHI Yong-yu1. Identification of human TIPE2 promoter and its regulatory regions [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(7): 39-43.
[9] LI Zhe1, YANG Ping2. Cognition level of law of the medical staff in Weihai and its related factors [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(3): 115-119.
[10] LI Zhe1, YANG Ping2. Cognition level of law of the medical staff in Weihai and its related factors [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(3): 115-119.
[11] ZHANG Li-juan,LIU Cai-hong, HU Yan-yan, LI Gui-mei. Effects of early intensive insulin therapy on the dynamics of  blood glucose and immunoloregulation on T lymphocyte  subgroups in non-obese diabetic mice [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(2): 49-53.
[12] YAO Fangmin1, SONG Dongfeng2, FU Wenqing1. Effect of the medical master students′ cognitive emotion regulation strategies on depression and anxiety [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2010, 48(5): 150-153.
[13] GUAN Hengyun1, ZHANG Ju1, ZHANG Pengju1, CHEN Weiwen1,  LIU Wenwen2, YU Chunxiao3, HU Xiaoyan1, JIANG Anli1
. Construction and expression of eukaryotic expression
plasmid of microRNA let7a2 in lung cancer cells
[J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2009, 47(02): 1-5.
[14] DU Juan,ZHANG Hong-jing,LI Yun,NIU Juan. Coping styles, emotion regulation and posttraumatic stress response in medical students [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2008, 46(2): 167-170.
[15] WANG Zhen-guang,SUN Shan-zhen,SHI Lin,WANG Dong-guan. Gene expression regulation between tongue squamous cell carcinoma cell line Tca-8113 and normal tongue mucosa fibroblasts [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2007, 45(5): 446-449.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!