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Hypoxia is a physiological cue that impacts diverse physiological processes, including energy metabolism, autophagy, cell motility, angiogenesis, and erythropoiesis. One of the key cell-autonomous effects of hypoxia is as a modulator of cell proliferation. For most cell types, hypoxia induces decreased cell proliferation, since an increased number of cells, with a consequent increase in O 2 demand, would only exacerbate hypoxic stress. However, certain cell populations maintain cell proliferation in the face of hypoxia. This is a common pathological hallmark of cancers, but can also serve a physiological function, as in the maintenance of stem cell populations that reside in a hypoxic niche. This review will discuss major molecular mechanisms by which hypoxia regulates cell proliferation in different cell populations, with a particular focus on the role of hypoxia-inducible factors.
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Maimon E. Hubbi
Gregg L. Semenza
AJP Cell Physiology
Johns Hopkins University
Johns Hopkins Medicine
The University of Texas Southwestern Medical Center
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Hubbi et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69dcc13a89c4deb67d359825 — DOI: https://doi.org/10.1152/ajpcell.00279.2015
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