Hypoxia-Inducible Factors in Cancer

Author:

Kim Laura C.1,Simon M. Celeste1ORCID

Affiliation:

1. Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Abstract

Abstract Low oxygen concentrations (hypoxia) are detrimental to most species on Earth; thus, cells have evolved with adaptations allowing them to withstand transient hypoxia. As with other survival pathways, cancer cells have co-opted these mechanisms to keep up with the metabolic demands of rapid growth and proliferation in harsh tumor microenvironments. The most well-studied oxygen response pathway involves hypoxia-inducible factors (HIF) and their regulation by the von Hippel–Lindau protein (pVHL) and the prolyl hydroxylases (PHD1-3). This study from Zhong and colleagues, published in Cancer Research in 1999, was the first to show increased HIF1α expression in several cancer types and in metastases, suggesting a role for HIFs in disease progression. Since publication, significant progress has been made in the understanding of tumor hypoxia responses and efforts to target this pathway as a therapeutic strategy for patients with cancer are underway. See related article by Zhong and colleagues, Cancer Res 1999;59:5830–5

Funder

NCI

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Reference10 articles.

1. Overexpression of hypoxia-inducible factor 1α in common human cancers and their metastases;Zhong;Cancer Res,1999

2. Cellular adaptation to hypoxia through hypoxia inducible factors and beyond;Lee;Nat Rev Mol Cell Biol,2020

3. HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression;Keith;Nat Rev Cancer,2012

4. The contribution of VHL substrate binding and HIF1-α to the phenotype of VHL loss in renal cell carcinoma;Maranchie;Cancer Cell,2002

5. Genetic and functional studies implicate HIF1α as a 14q kidney cancer suppressor gene;Shen;Cancer Discov,2011

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3