Targeting p53 in Cancer

ISSN: 1875-5992 (Online)
ISSN: 1871-5206 (Print)


Volume 16, 12 Issues, 2016


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Anti-Cancer Agents in Medicinal Chemistry

Formerly: Current Medicinal Chemistry - Anti-Cancer Agents

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  • 27th of 59 in Chemistry, Medicinal

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Editor-in-Chief:
Michelle Prudhomme
Universite Blaise Pascal - C.N.R.S
Aubiere Cedex
France


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Targeting p53 in Cancer



Anti-Cancer Agents in Medicinal Chemistry, 1(2): 151-161.

Author(s): Patrick Chene.

Affiliation: Novartis, K125 420, CH-4002Basel Switzerland.

Abstract

The loss of p53 function is a very important event in cancer. The absence of a functional p53 in tumours favours cancer development, and it has been suggested that it also influences the efficacy of both chemotherapy and radiotherapy. The p53 pathway is therefore the subject of intense research, both in academia and in industry, to identify new compounds targeting tumours with an altered p53. Different strategies are currently under investigation. They can be divided into two groups: biological and chemical strategies. The biological strategies utilise the immune system to eliminate the tumours overexpressing p53 mutants. Alternatively they use vectors delivering a functional p53 gene in tumours or engineered viruses, which selectively target p53-defective cells. The chemical strategies are based on the design of compounds that stabilise or activate the p53 mutant proteins, inhibit the interaction between p53 and hdm2, or act on the p53-binding chaperone proteins. In this review, the current progress in these different approaches will be analysed.

Keywords:

targeting, cancer, gene replacement therapy, Immunotherapy, engineered viruese, targeting mutants, antioxidants.



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Article Details

Volume: 1
Issue Number: 2
First Page: 151
Last Page: 161
Page Count: 11
DOI: 10.2174/1568011013354741
Price: $58
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