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Updated: Jul 10, 2026

Method for Novel Anti-Cancer Drug Development using Tumor Explants of Surgical Specimens
Published on: July 29, 2011
American Association for Cancer Research 1998: promises and prospects for the next century
1Rhône-Poulenc Rorer, Centre de Recherche de Vitry-Alfortville, F 94403 Vitry-sur-Seine Cedex, France.
Abstract:
The American Association for Cancer Research (AACR) meeting of this year highlighted the progress made with farnesyl transferase inhibitors; two compounds have now entered Phase I clinical trials: R 115777 (Janssen) and SCH 66336 (Schering Plough) and several others are nearing clinical testing. Several new protein kinase inhibitors from Warner Lambert and Novartis were also discussed. Angiogenesis (as well as apoptosis) also featured, with many pharmaceutical companies and academic institutions having programmes in this area of cancer research. The most promising second generation compounds are angiostatin/endostatin and inhibitors of tyrosine protein kinase from the vascular endothelial growth factor (VEGF) receptor, including SU 5416 which is in clinical trials.
Insights
Cancer research advances include farnesyl transferase inhibitors and protein kinase inhibitors entering clinical trials. Promising angiogenesis inhibitors targeting vascular endothelial growth factor (VEGF) receptors are also in development.
Area of Science:
- Oncology
- Pharmacology
Background:
- The American Association for Cancer Research (AACR) meeting showcased advancements in cancer therapy development.
- Key areas of focus included farnesyl transferase inhibitors and protein kinase inhibitors.
Purpose of the Study:
- To summarize recent progress in cancer drug development presented at the AACR meeting.
- To highlight promising therapeutic targets and compounds in preclinical and clinical development.
Main Methods:
- Review of presentations and discussions from the AACR meeting.
- Identification of key drug classes and specific compounds under investigation.
Main Results:
- Two farnesyl transferase inhibitors (R 115777 and SCH 66336) have advanced to Phase I clinical trials.
- Several other farnesyl transferase inhibitors and new protein kinase inhibitors are nearing clinical testing.
- Angiogenesis inhibitors, including angiostatin/endostatin and vascular endothelial growth factor (VEGF) receptor tyrosine kinase inhibitors like SU 5416, show significant promise and are in clinical trials.
Conclusions:
- Significant progress is being made in the development of novel cancer therapeutics.
- Targeting farnesyl transferase, protein kinases, and angiogenesis pathways represents key strategies in current cancer research.
- Clinical trials are validating the therapeutic potential of these emerging cancer drug candidates.
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