Variances in the Expression Profile of the EMT-Related Genes in Endometrial Cancer Lines In Vitro Study

被引:3
作者
Nowakowski, Robert [1 ,2 ]
Grabarek, Beniamin [1 ,2 ,3 ]
Burnat-Olech, Anna [1 ]
Boron, Dariusz [1 ,2 ,3 ]
Paul-Samojedny, Monika [4 ]
机构
[1] Univ Technol Katowice, Fac Med, Dept Histol Cytophysiol & Embryol, PL-41800 Zabrze, Poland
[2] Dist Hosp Chrzanow, PL-32500 Chrzanow, Poland
[3] Ludwik Rydygier Mem Specialized Hosp, Dept Gynecol & Obstet Gynecol Oncol, PL-31826 Krakow, Poland
[4] Med Univ Silesia, Div Lab Med, Sch Pharm, Dept Med Genet, Jednosci 8, PL-41200 Sosnowiec, Poland
关键词
Cisplatin; endometrial cancer; cell line; mRNA; miRNA; epithelial-mesenchymal transition; EPITHELIAL-MESENCHYMAL TRANSITION; TGF-BETA/SMAD; CISPLATIN; MICROBIOTA; RNA;
D O I
10.2174/1389201022666210702153919
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The aim of the study was to evaluate the variances in the expression pattern of mRNAs and miRNAs related to the EMT in the Ishikawa (histological grade 1; G1), EC-1A (histological grade 2; G2), and KLE (histological grade 3; G3) cell cultures under cisplatin treatment. Methods: Endometrial cancer cell lines were exposed to 75.22 mg (an average concentration of the drug used in patients with endometrial cancer) for 12.24 and 48 hours in comparison to the untreated cells (control). The molecular analysis included: extraction of total RNA, microarray analysis (mRNA and miRNA), RTqPCR, and the ELISA assay. Results: Out of 226 mRNAs associated with the EMT, the number of mRNAs differentially expressed in endometrial cancer cell cultures treated with cisplatin compared to a control culture was as follows: Ishikawa line -87 mRNAs; EC-1A -84 mRNAs; KLE -71 mRNAs (p<0.05). The greatest changes in the Ishikawa line treated with the drug compared to the control were noticed for mRNA STAT1 TGF131, SMAD3, FOXO8, whereas in EC-1A they were mRNA TGF131, BAMBI, SMAD4, and in KLE mRNA COL1A1, FOXO8, TGF131. The analysis also showed that miR-106a, miR-30d, miR-300 are common for all cell lines used in this experiment. Conclusion: Cisplatin changes the expression profile of genes associated with EMT in endometrial cancer cell lines. It seems that the expression pattern of TGF131 might be a promising, supplementary molecular marker of the effectiveness of cisplatin therapy. The analysis showed that miR-30d, miR-300, and miR-106a are involved in the regulation of the expression of EMT-related genes.
引用
收藏
页码:594 / 608
页数:15
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