Establishment of two oxaliplatin-resistant gallbladder cancer cell lines and comprehensive analysis of dysregulated genes

Author:

Guo Haijun1,Zhi Yunqing2,Wang Kaijing3,Li Na4,Yu Danlei4,Ji Zhonghua5,Chen Bo6

Affiliation:

1. Department of Emergency Surgery, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital , Shanghai 201318 , China

2. Department of Assisted Reproductive Medicine, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine , Shanghai 201204 , China

3. Department of Hepatobiliary Surgery, Shanghai East Hospital, Tongji University School of Medicine , Shanghai 200120 , China

4. Department of Nursing, Shanghai East Hospital, Tongji University School of Medicine , Shanghai 200120 , China

5. Department of Anesthesia, Shanghai East Hospital, Tongji University School of Medicine , 150 Jimo Road , Shanghai 200120 , China

6. Department of Hepatobiliary Surgery, Shanghai East Hospital, Tongji University School of Medicine , 150 Jimo Road , Shanghai 200120 , China

Abstract

Abstract Acquired resistance to chemotherapeutic drugs in gallbladder cancer (GBC) results in therapy failure. This study is aimed to establish oxaliplatin (OXA)-resistant GBC cell lines and uncover their gene expression profiles. First, two OXA-resistant GBC cell lines (GBC-SD/OXA and SGC996/OXA) were established by gradually increasing the drug concentration, and the resistance index was 4–5. The two resistant cell lines showed slower proliferation and higher stemness, colony formation, and migration abilities. Epithelial mesenchymal transformation and increased levels of P-glycoprotein were also detected. Next RNA-sequence analysis identified 4,675 dysregulated genes (DGs) in resistant cells, and most of the 12 randomly selected DGs were verified to be consistent with the sequence results. Kyoto Encyclopedia of Genes and Genomes analysis indicated that several DGs were involved in resistance- and phenotype-related pathways, of which the activations of PD-L1 and ERK1/2 were both verified in resistant cell lines. In conclusion, this study is the first to report the gene expression profile of OXA-resistant GBC cells and provides a useful database for target development.

Publisher

Walter de Gruyter GmbH

Subject

General Medicine

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