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Updated: Oct 9, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Modulation of oncogene and tumor-suppressor gene expression: a novel strategy for cancer prevention and treatment
1Department of Thoracic Surgery, University of Texas M. D. Anderson Cancer Center, Houston 77030.
Background:
Advances in our understanding of the molecular biology of cancer have the potential for translation into clinical cancer prevention and treatment strategies. Oncogenes and tumor suppressor genes have been implicated in the development of human cancers Mutations in gene families occur in both premalignant lesions and invasive tumors.
Conclusion:
Recombinant DNA constructs can be made that eliminate expression of a mutant oncogene protein or provide a normal copy of a tumor suppressor gene to the cancer cell. Reversal of a single genetic lesion is sufficient to inhibit cancer cell proliferation and tumorigenicity. Viral vectors are now being evaluated for direct delivery of these constructs to human tumors.
Insights
Targeting cancer genes with gene therapy shows promise. Reversing genetic mutations in oncogenes or tumor suppressor genes can stop cancer growth and tumor formation, with viral vectors being explored for delivery.
Area of Science:
- Molecular oncology
- Cancer genetics
- Gene therapy
Background:
- Cancer development involves oncogenes and tumor suppressor genes.
- Mutations in these genes occur in premalignant and invasive tumors.
- Understanding cancer's molecular biology aids prevention and treatment.
Purpose of the Study:
- To explore the potential of gene therapy in cancer treatment.
- To investigate the impact of correcting genetic lesions on cancer cells.
Main Methods:
- Utilizing recombinant DNA constructs to modify gene expression.
- Developing strategies to eliminate mutant oncogene proteins.
- Introducing normal tumor suppressor gene copies into cancer cells.
Main Results:
- Reversal of single genetic lesions inhibited cancer cell proliferation.
- Correction of genetic defects reduced tumor formation.
- Demonstrated the efficacy of targeting specific gene families.
Conclusions:
- Gene therapy offers a viable strategy for cancer treatment.
- Eliminating mutant oncogene expression or providing functional tumor suppressor genes halts cancer progression.
- Viral vectors are under investigation for targeted gene delivery to tumors.
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