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Updated: Apr 3, 2026

Discovery of Driver Genes in Colorectal HT29-derived Cancer Stem-Like Tumorspheres
Published on: July 22, 2020
Gene and protein expression in the oxaliplatin-resistant HT29/L-OHP human colon cancer cell line
1Department of Gastrointestinal Surgery, The First Affiliated Hospital of Chongqing Medical University.
Abstract:
Oxaliplatin (L-OHP) is one of the most commonly used anticancer drugs in adjuvant treatment of colon cancer after complete resection of the primary tumor and treatment of metastatic colorectal cancer. Cancer cells eventually become resistant to L-OHP, which diminishes its curative effect. However, the mechanism of action of L-OHP remains unknown. In this study, an L-OHP-resistant human colon cancer cell line, HT29/L-OHP, was established by gradually increasing the dose of L-OHP in culture. The expression levels of the tumor susceptibility gene 101 (tsg101) and the TSG101 protein in HT29 and HT29/L-OHP cell lines were examined by reverse transcription-polymerase chain reaction and western blot analysis. In addition, the expression levels of several apoptosis-regulating protein markers were determined using immunohistochemistry-staining assays. We found that the expression of tsg101 mRNA and of TSG101 protein were significantly higher in the HT29/L-OHP cell line than in its parent, HT29 (P < 0.05). In addition, the expression of multiple apoptosis-regulating protein markers were significantly increased (P < 0.05) in the HT29/L-OHP cell line. These data suggest that these markers could be useful as predictive markers for evaluating and comparing the efficacy and molecular pharmacology of chemotherapeutics.
Insights
Oxaliplatin resistance in colon cancer cells is linked to increased expression of tumor susceptibility gene 101 (TSG101). This finding may help predict chemotherapy effectiveness.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Oxaliplatin (L-OHP) is a key chemotherapy agent for colorectal cancer.
- Acquired resistance to L-OHP limits its therapeutic efficacy.
- The molecular mechanisms underlying L-OHP resistance are not fully understood.
Purpose of the Study:
- To investigate the role of tumor susceptibility gene 101 (TSG101) in L-OHP resistance.
- To identify potential biomarkers for predicting L-OHP efficacy.
Main Methods:
- Established an L-OHP-resistant human colon cancer cell line (HT29/L-OHP).
- Analyzed TSG101 mRNA and protein expression using RT-PCR and Western blot.
- Assessed apoptosis-regulating protein markers via immunohistochemistry.
Main Results:
- TSG101 mRNA and protein levels were significantly elevated in HT29/L-OHP cells compared to parental HT29 cells.
- Expression of several apoptosis-regulating proteins was also significantly increased in resistant cells.
Conclusions:
- Increased TSG101 expression is associated with L-OHP resistance in colon cancer.
- TSG101 and apoptosis markers may serve as predictive biomarkers for L-OHP treatment efficacy.

