HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Ribosomal proteins S13 and L23 promote multidrug resistance in gastric cancer cells by suppressing drug-induced apoptosis.

Abstract
Ribosomal proteins (RP) S13 and RPL23 were previously identified as two upregulated genes in a multidrug-resistant gastric cancer cell line SGC7901/VCR compared to its parental cell SGC7901 by differential display PCR. The aim of this study was to explore the roles of RPS13 and RPL23 in multidrug resistance (MDR) in gastric cancer cells. RPS13 and RPL23 were genetically overexpressed in SGC7901 cells, respectively. Either RPS13 or RPL23 enhanced resistance of SGC7901 cells to vincristine, adriamycin, and 5-fludrouracil. RPL23 also enhanced resistance of SGC7901 cells to cisplatin. Overexpression of either RPS13 or RPL23 did not alter the population doubling time, [3H]leucine incorporation, and intracellular adriamycin accumulation of SGC7901 cells. However, either RPS13 or RPL23 could protect SGC7901 cells from undergoing vincristine-induced apoptosis. Western blot analysis revealed that both RPS13 and RPL23 significantly increased the expression level of Bcl-2 and Bcl-2/Bax ratio in SGC7901 cells. In addition, overexpression of RPL23 enhanced glutathione S-transferase (GST) activity and intracellular glutathione content in SGC7901 cells. Together, this work demonstrates that either RPS13 or RPL23 can promote MDR in gastric cancer cells by suppressing drug-induced apoptosis, and that RPL23 may also promote MDR in gastric cancer cells through regulation of glutathione S-transferase-mediated drug-detoxifying system.
AuthorsYongquan Shi, Huihong Zhai, Xin Wang, Zheyi Han, Changjiang Liu, Mei Lan, Jingping Du, Changcun Guo, Yumei Zhang, Kaichun Wu, Daiming Fan
JournalExperimental cell research (Exp Cell Res) Vol. 296 Issue 2 Pg. 337-46 (Jun 10 2004) ISSN: 0014-4827 [Print] United States
PMID15149863 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • BAX protein, human
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • RPS13 protein, human
  • Ribosomal Proteins
  • bcl-2-Associated X Protein
  • ribosomal protein L17
  • Vincristine
  • Glutathione Transferase
Topics
  • Apoptosis (drug effects)
  • Cell Division
  • Cell Line, Tumor
  • Drug Resistance, Multiple
  • Glutathione Transferase (metabolism)
  • Humans
  • Neoplasm Proteins (physiology)
  • Proto-Oncogene Proteins (analysis)
  • Proto-Oncogene Proteins c-bcl-2 (analysis)
  • Ribosomal Proteins (genetics, physiology)
  • Stomach Neoplasms (pathology)
  • Transfection
  • Vincristine (pharmacology)
  • bcl-2-Associated X Protein

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: