Interactions between microRNA-200 family and Sestrin proteins in endometrial cancer cell lines and their significance to anoikis

被引:30
作者
Kozak, Joanna [1 ]
Wdowiak, Paulina [1 ]
Maciejewski, Ryszard [1 ]
Torres, Anna [1 ]
机构
[1] Med Univ Lublin, Dept Normal Anat, PL-20090 Lublin, Poland
关键词
Endometrial cancer; Sestrin; miR-141; miR-200a; Luciferase reporter assay; Anoikis; AUTOPHAGIC DEGRADATION; EXPRESSION; STRESS; TARGET; KEAP1; NRF2;
D O I
10.1007/s11010-019-03547-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the present study, we intend to determine whether Sestrin proteins 1, 2, and 3 (SESN1-3) are targets of microRNA-200 family (miR-200) in endometrial cancer (EC) Ishikawa, AN3CA, KLE, and RL 95-2 cell lines and to investigate how these potential interactions influence anoikis resistance of EC cell lines. The luciferase reporter assay, qRT-PCR, and western blotting assays were used to verify whether SESN1-3 are direct targets of miR-200. Moreover, the anoikis assay and transient transfections of miR-200 mimics or inhibitors into EC cell lines were performed to evaluate the modulatory role of miR-200 and SESN proteins on anoikis resistance. We demonstrated that SESN2 protein is a direct target of mir-141 in KLE and RL-95-2 EC cell lines and the functional interaction of miR-141 and SESN2 protein has a downstream effect on anoikis resistance and SESN2 expression level in Ishikawa and AN3CA cell lines. Moreover, we have shown that SESN3 protein is a direct target of miR-200b, miR-200c, and miR-429 in Ishikawa, AN3CA, and KLE cell lines. Our results show that manipulation of miR-200b, miR-200c, and miR-429 expression patterns also has an influence on anoikis resistance in EC cell lines. In conclusion, we identified new interactions between miR-200 and the oxidative stress response SESN proteins that affect anoikis resistance in human EC cells.
引用
收藏
页码:21 / 34
页数:14
相关论文
共 42 条
[1]  
Aldred S. F., 2011, JOVE-J VIS EXP, V55, P3343, DOI DOI 10.3791/
[2]   Sestrins Activate Nrf2 by Promoting p62-Dependent Autophagic Degradation of Keap1 and Prevent Oxidative Liver Damage [J].
Bae, Soo Han ;
Sung, Su Haeng ;
Oh, Sue Young ;
Lim, Jung Mi ;
Lee, Se Kyoung ;
Park, Young Nyun ;
Lee, Hye Eun ;
Kang, Dongmin ;
Rhee, Sue Goo .
CELL METABOLISM, 2013, 17 (01) :73-84
[3]   Advances in the Management of Recurrent Endometrial Cancer [J].
Bradford, Leslie S. ;
Rauh-Hain, Jose Alejandro ;
Schorge, John ;
Birrer, Michael J. ;
Dizon, Don S. .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2015, 38 (02) :206-212
[4]   Stressin' Sestrins take an aging fight [J].
Budanou, Andrei V. ;
Lee, Jun Hee ;
Karin, Michael .
EMBO MOLECULAR MEDICINE, 2010, 2 (10) :388-400
[5]   p53 target genes Sestrin1 and Sestrin2 connect genotoxic stress and mTOR signaling [J].
Budanov, Andrei V. ;
Karin, Michael .
CELL, 2008, 134 (03) :451-460
[6]   Regeneration of peroxiredoxins by p53-regulated sestrins, homologs of bacterial AhpD [J].
Budanov, AV ;
Sablina, AA ;
Feinstein, E ;
Koonin, EV ;
Chumakov, PM .
SCIENCE, 2004, 304 (5670) :596-600
[7]   Identification of a novel stress-responsive gene Hi95 involved in regulation of cell viability [J].
Budanov, AV ;
Shoshani, T ;
Faerman, A ;
Zelin, E ;
Kamer, I ;
Kalinski, H ;
Gorodin, S ;
Fishman, A ;
Chajut, A ;
Einat, P ;
Skaliter, R ;
Gudkov, AV ;
Chumakov, PM ;
Feinstein, E .
ONCOGENE, 2002, 21 (39) :6017-6031
[8]   Discordant protein and mRNA expression in lung adenocarcinomas [J].
Chen, GA ;
Gharib, TG ;
Huang, CC ;
Taylor, JMG ;
Misek, DE ;
Kardia, SLR ;
Giordano, TJ ;
Iannettoni, MD ;
Orringer, MB ;
Hanash, SM ;
Beer, DG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (04) :304-313
[9]   The Functions of MicroRNA-200 Family in Ovarian Cancer: Beyond Epithelial-Mesenchymal Transition [J].
Choi, Pui-Wah ;
Ng, Shu-Wing .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (06)
[10]   MicroRNA-200b Is Overexpressed in Endometrial Adenocarcinomas and Enhances MMP2 Activity by Downregulating TIMP2 in Human Endometrial Cancer Cell Line HEC-1A Cells [J].
Dai, Yinmei ;
Xia, Wei ;
Song, Tao ;
Su, Xueting ;
Li, Jie ;
Li, Shaohua ;
Chen, Ying ;
Wang, Wei ;
Ding, Hongmei ;
Liu, Xuemei ;
Li, Hui ;
Zhao, Qiang ;
Shao, Ningsheng .
NUCLEIC ACID THERAPEUTICS, 2013, 23 (01) :29-34