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Journal article

Hypoxia and HIF pathway in cancer and the placenta

Abstract:
In this review we note that the placenta and cancer both develop in microenvironments in which there are gradients of oxygen availability. Whilst fundamentally different in that placental development is organised and physiological whilst cancer is chaotic and pathological, there are similarities in their respective capacities to proliferate, invade adjacent tissues, generate a blood supply and avoid rejection by the immune system. We provide a brief description of the hypoxia-inducible factor (HIF) pathway and indicate the ways by which HIF activity can be regulated to achieve oxygen homeostasis. We then exemplify the potential role of the HIF pathway in contributing to those functions shared between the placenta and cancer through effects on cellular proliferation, cell death, angiogenesis, blood vessel co-option, vascular mimicry, cell adhesion molecules, secretion of matrix metalloproteinases, antigen presentation mechanisms and immunosuppressive factors. We advocate future studies to explore these similarities and differences in the hope of improving our understanding of both systems and hence treatments of placental disorders and cancer.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.placenta.2017.03.010

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Societies, Other & Subsidiary Companies
Department:
Kellogg College
Oxford college:
Kellogg College
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Oxford Ludwig Institute
Role:
Author



Publisher:
Elsevier
Journal:
Placenta More from this journal
Volume:
56
Pages:
8-13
Publication date:
2017-03-01
Acceptance date:
2017-03-14
DOI:
EISSN:
1532-3102
ISSN:
0143-4004


Language:
English
Keywords:
Pubs id:
pubs:687814
UUID:
uuid:d7af423f-3579-42ea-91d2-94d4b396578e
Local pid:
pubs:687814
Source identifiers:
687814
Deposit date:
2017-04-13

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