期刊
NEOPLASIA
卷 20, 期 2, 页码 131-139出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.neo.2017.11.010
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资金
- NIH [R01CA73850, R01CA82237, R35CA209960, P30CA006973]
- NATIONAL CANCER INSTITUTE [R35CA209960, R01CA082337, R01CA136576] Funding Source: NIH RePORTER
Hypoxia inducible factors (HIFs) are transcription factors that mediate the response of cells to hypoxia. HIFs have wide-ranging effects on metabolism, the tumor microenvironment (TME) and the extracellular matrix (ECM). Here we investigated the silencing effects of two of the three known isoforms, HIF-1 alpha and HIF-2 alpha, on collagen 1 (Col1) fibers, which form a major component of the ECM of tumors. Using a loss-of-function approach for HIF-1 alpha or 2 alpha or both HIF-1 alpha and 2 alpha, we identified a relationship between HIFs and Col1 fibers in MDA-MB-231 tumors. Tumors derived from MDA-MB-231 cells with HIF-1 alpha or 2 alpha or both HIF-1 alpha and 2 alpha silenced contained higher percent fiber volume and lower inter-fiber distance compared to tumors derived from empty vector MDA-MB-231 cells. Depending upon the type of silencing, we observed changes in Col1 degrading enzymes, and enzymes involved in Col1 synthesis and deposition. Additionally, a reduction in lysyl oxidase protein expression in HIF-down-regulated tumors suggests that more non-cross-linked fibers were present. Collectively these results identify the role of HIFs in modifying the ECM and the TME and provide new insights into the effects of hypoxia on the tumor ECM.
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