Long non-coding RNA tumor suppressor candidate 7 advances chemotherapy sensitivity of endometrial carcinoma through targeted silencing of miR-23b.

作者: Chao Shang , Bin Lang , Cheng Ngok Ao , Lirong Meng

DOI: 10.1177/1010428317707883

关键词:

摘要: Endometrial carcinoma is the most common malignant tumor of female genital tract worldwide. TUSC7 (tumor suppressor candidate 7) an antisense long non-coding RNA and downregulated acts as a potential in several tumors. In this study, low expression was confirmed endometrial tissues associated with high pathological stages carcinoma, which revealed that might be involved tumorigenesis progression carcinoma. Moreover, cell lines resistant to CDDP Taxol lower than sensitive lines, indicated level positively correlated response patients chemotherapy Taxol. upregulation inhibited proliferation, blocked cells at G1 phase, advanced apoptosis sensitivity HEC1A/CR line. Furthermore, miR-23b upregulated negatively TUSC7. pull-down assay could specifically silence line; target gene MiR-23b mostly reversed TUSC7-induced regulatory effects on summary, underexpressed especially chemotherapy-resistant acted inhibit growth well advance through targeted silencing miR-23b, provide new therapeutic

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