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

Open Med (Wars)

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

Published: September 2023

AI Article Synopsis

  • This study investigates acquired resistance to oxaliplatin (OXA), a chemotherapeutic drug, in gallbladder cancer (GBC) by creating OXA-resistant GBC cell lines.
  • Two OXA-resistant cell lines exhibited slower growth rates and enhanced abilities in stemness, colony formation, and migration, along with notable changes in gene expression.
  • The research identifies key dysregulated genes and pathways, particularly highlighting the role of PD-L1 and ERK1/2 in drug resistance, providing a foundation for future targeted therapies.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541806PMC
http://dx.doi.org/10.1515/med-2023-0690DOI Listing

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