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Knockdown of IGF- I R by antisense oligodeoxynucleotide auguments sensitivity of T24 bladder cancer cells to mitomycin

  • Weizmann Institute of Science

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

AIM: To investigate whether insulin-like growth factor I receptor (IGF- I R) was involved in drug resistance of bladder cancer cells. METHODS: RT-PCR was used to detect the mRNA expression of IGF- I, IGF- II, and IGF- I R in T24 cells and normal urothelial cells. Flow cytometry and MTT tests were used to assess the effect of antisense oligodeoxynucleotide (ODN) on drug sensitivities and apoptosis of T24 cells to mitomycin (MMC). Western blot was used to analyze the effect of ODN on expression of IGF- I R protein. RESULTS: mRNA of IGF- I, IGF- II, and IGF- I R were strongly expressed in serum-free cultured T24 cell line, whereas normal urothelial cells did not express these factors/receptors or only in trace levels; knockdown of IGF- I R by antisense ODN greatly inhibited the growth of bladder cancer cells and enhanced sensitivity and apoptosis of T24 cells to MMC. CONCLUSION: These results suggested that blockage of IGF- I R signaling might potentially contribute to the treatment of bladder cancer cells which were insensitive to chemotherapy.

Original languageEnglish
Pages (from-to)841-846
Number of pages6
JournalActa Pharmacologica Sinica
Volume22
Issue number9
StatePublished - 2001
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Autocrine
  • Bladder neoplasms
  • Drug resistance
  • Insulin-like growth factor I
  • Receptors

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