4.6 Article

In vivo and in vitro effects of a HIF-1α inhibitor, RX-0047

Journal

JOURNAL OF CELLULAR BIOCHEMISTRY
Volume 104, Issue 3, Pages 985-994

Publisher

WILEY
DOI: 10.1002/jcb.21681

Keywords

hypoxia; HIF-1 alpha; RX-0047; cancer; bioluminescence imaging

Funding

  1. NCI NIH HHS [P20 CA86354, P20 CA086354, P50 CA070907, CA70907] Funding Source: Medline

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HIF-1 alpha plays a major role in activating gene transcription and is important for maintaining homeostasis under hypoxic conditions. Since tumors are often in a hypoxic state, HIF-1 alpha is a potential target for the development of novel cancer therapeutics. This study was performed to determine the antitumoral efficacy of an antisense HIF-1 alpha inhibitor, RX-0047 on different human cancer cell lines (MDA-MB 231, HME50-T, PC-3, Panc-1 and A549) in vitro. A549 lung cancer and PC-3 prostate cancer cells containing a luciferase gene reporter were used for in vivo xenograft animal models. Progressive tumor development was quantified using live animal BLI (bioluminescence imaging) in addition to ex vivo imaging and histology. All cell lines tested were sensitive to inhibition of cell growth with 10 nM and higher ranges of RX-0047, additionally RX-0047 sensitizes cells to ionizing radiation treatments. Finally, RX-0047 (30 mg/kg) inhibited the formation of human lung metastasis in xenograft mouse models and reduced tumor size in flank models.

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