1. Academic Validation
  2. Natural product-based inhibitors of hypoxia-inducible factor-1 (HIF-1)

Natural product-based inhibitors of hypoxia-inducible factor-1 (HIF-1)

  • Curr Drug Targets. 2006 Mar;7(3):355-69. doi: 10.2174/138945006776054979.
Dale G Nagle 1 Yu-Dong Zhou
Affiliations

Affiliation

  • 1 Department of Pharmacognosy, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS 38677-1848, USA. dnagle@olemiss.edu
Abstract

The transcription factor hypoxia-inducible factor-1 (HIF-1) regulates the expression of more than 70 genes involved in cellular adaptation and survival under hypoxic stress. Activation of HIF-1 is associated with numerous physiological and pathological processes that include tumorigenesis, vascular remodeling, inflammation, and hypoxia/ischemia-related tissue damage. Clinical studies suggested that HIF-1 activation correlates directly with advanced disease stages and treatment resistance among Cancer patients. Preclinical studies support the inhibition of HIF-1 as a major molecular target for antitumor drug discovery. Considerable effort is underway, in government laboratories, industry and academia, to identify therapeutically useful small molecule HIF-1 inhibitors. Natural Products (low molecular weight organic compounds produced by Plants, microbes, and Animals) continue to play a major role in modern antitumor drug discovery. Most of the compounds discovered to inhibit HIF-1 are Natural Products or synthetic compounds with structures that are based on natural product leads. Natural Products have also served a vital role as molecular probes to elucidate the pathways that regulate HIF-1 activity. Natural Products and natural product-derived compounds that inhibit HIF-1 are summarized in LIGHT of their biological source, chemical class, and effect on HIF-1 and HIF-mediated gene regulation. When known, the mechanism(s) of action of HIF-1 inhibitors are described. Many of the substances found to inhibit HIF-1 are non-druggable compounds that are too cytotoxic to serve as drug leads. The application of high-throughput screening methods, complementary molecular-targeted assays, and structurally diverse chemical libraries hold promise for the discovery of therapeutically useful HIF-1 inhibitors.

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