lncRNA-CCAT2 Reduces the Drug Resistance of Ovarian Cancer Cells

Author:

Zhou Jianyun1,Wang Xiumei1,Han Yun2,Chu Qiaoxiang1,Zheng Yanli2

Affiliation:

1. Department of Gynecology, Haian People’s Hospital Affiliated to Nantong University, Nantong, Jiangsu, 226600, China

2. Department of Gynecology, The Second Affiliated Hospital of Nantong University (Nantong First People’s Hospital), Nantong, Jiangsu, 226006, China

Abstract

This study assesses lncRNA-CCAT2’s role in reducing the drug resistance of ovarian cancer cell lines. Cisplatin-resistant SKOV-3/DDP cells were established and assigned into CC group (transfected with lncRNA CCAT2 siRNA-NC) and CA group (transfected with lncRNA CCAT2 siRNA) followed by analysis of cell proliferation, apoptosis, expression of CCAT2, ERK1/2, Sp1 and relationship between CCAT2 and ERK1/2 and Sp1. CCAT2 expression in SKOV-3/DDP was higher than IOSE80 and SKOV-3 (P < 0.001). ERK1/2 expression in SKOV-3 and SKOV-3/DDP was 0.67±0.09, 1.97±0.40 (t = 14.18, P < 0.001). Sp1 level in SKOV-3 and SKOV-3/DDP was 0.49±0.05, 1.07±0.11 (P = 21.47, P < 0.001). Transfection of CCAT2 reduced cell fluorescence activity of ERK1/2 and Sp1 (P < 0.001). Cell proliferation in CC group and CA group had no difference at 0 h (P > 0.001) and the inhibition of cell proliferation was found at 24 h (P < 0.001). CC group (5.13±0.51) had lower cell apoptosis rate than CA group (20.52±2.24) (t = 29.96, P < 0.001) but higher ERK1/2 and Sp1 protein level CC group than CA group (P < 0.001). In conclusion, transfection of lncRNA-CCAT2 inhibits SKOV-3/DDP proliferation by targeting ERK1/2-Sp1 signaling pathway, promotes apoptosis and reduces drug resistance.

Publisher

American Scientific Publishers

Subject

Biomedical Engineering,Medicine (miscellaneous),Bioengineering,Biotechnology

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