[Detection of drug resistant-genes in cisplatin-resistant colon carcinoma cells by RT-PCR assay. II]

T Funato1, T Tone, H Miyachi

  • 1Department of Clinical and Laboratory Medicine, Tohoku University School of Medicine, Sendai.

Rinsho Byori. the Japanese Journal of Clinical Pathology
|February 1, 1993
PubMed

Insights

The study found that oncogenes c-fos, c-Ha-ras, and c-myc mRNA levels increase in cisplatin-resistant colon cancer cells. Reverse transcription PCR (RT-PCR) can detect these changes for early identification of cisplatin resistance.

Area of Science:

  • Molecular biology
  • Cancer genetics
  • Oncogene research

Context:

  • The role of oncogenes in DNA synthesis is crucial.
  • Colon carcinoma cell lines provide a model for cancer research.
  • Cisplatin resistance is a significant challenge in cancer therapy.

Purpose:

  • To compare the expression of c-fos, c-Ha-ras, and c-myc oncogenes in cisplatin-sensitive and cisplatin-resistant human colon carcinoma cells.
  • To evaluate the utility of the reverse transcription PCR (RT-PCR) method for detecting oncogene expression changes related to cisplatin resistance.

Summary:

  • Expression of c-fos, c-Ha-ras, and c-myc oncogenes was significantly upregulated in cisplatin-resistant HCT8DDP cells compared to parent HCT8S cells.
  • Northern blotting analysis revealed fold increases in mRNA for these oncogenes in resistant cells.
  • Reverse transcription PCR (RT-PCR) proved effective in quantifying oncogene expression, even from minimal cell samples.

Impact:

  • The findings suggest that increased expression of these oncogenes is associated with cisplatin resistance in colon cancer.
  • RT-PCR assay shows potential as an early detection tool for identifying oncogenes linked to cisplatin resistance.
  • This research contributes to understanding mechanisms of drug resistance and developing targeted therapies.