| Literature DB >> 31981591 |
Yiyi Zhang1, Lijun Sun2, Yanwu Sun1, Ying Chen3, Xiaojie Wang1, Meifang Xu4, Pan Chi1, Zongbin Xu5, Xingrong Lu6.
Abstract
CES-2 (carboxylesterase-2) belongs to the carboxylesterase gene family, which plays crucial roles in lipid mobilization and chemosensitivity to irinotecan. However, its role in chemosensitivity to oxaliplatin (L-OHP) remains unclear. Herein, L-OHP-resistant cells (HCT-116L and RKOL) were established by increasing the concentration of L-OHP. The results showed that CES2 expression was upregulated in L-OHP-resistant tissues and cells lines (both P < 0.01). Low expression of CES2 correlated with a better survival, and the results were further confirmed in the R2 platform: a biologist friendly web-based genomics analysis and visualization application. Downregulation of CES2 suppressed cell proliferation, induced apoptosis and reversed L-OHP resistance by medicating the PI3K signaling pathway in L-OHP-resistant cells. However, both PI3K inhibitor (LY294002) and activator (IGF-1) could not medicate CES2 expression. These findings indicated that CES2 may be utilized as a novel biomarker and therapeutic target for L-OHP resistance in CRC treatment.Entities:
Keywords: Carboxylesterase-2; Chemotherapy resistance; Colorectal cancer; Oxaliplatin; PI3K signaling pathway
Year: 2020 PMID: 31981591 DOI: 10.1016/j.yexcr.2020.111856
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905