Hypoxic control of metastasis

Author:

Rankin Erinn B.12,Giaccia Amato J.1

Affiliation:

1. Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University Medical Center, Stanford, CA 94305-5152, USA.

2. Department of Obstetrics and Gynecology, Stanford University Medical Center, Stanford, CA 94305-5152, USA.

Abstract

Metastatic disease is the leading cause of cancer-related deaths and involves critical interactions between tumor cells and the microenvironment. Hypoxia is a potent microenvironmental factor promoting metastatic progression. Clinically, hypoxia and the expression of the hypoxia-inducible transcription factors HIF-1 and HIF-2 are associated with increased distant metastasis and poor survival in a variety of tumor types. Moreover, HIF signaling in malignant cells influences multiple steps within the metastatic cascade. Here we review research focused on elucidating the mechanisms by which the hypoxic tumor microenvironment promotes metastatic progression. These studies have identified potential biomarkers and therapeutic targets regulated by hypoxia that could be incorporated into strategies aimed at preventing and treating metastatic disease.

Funder

NIH

Silicon Valley Foundation

Sydney Frank Foundation

Kimmelman Fund

Department of Defense Ovarian Cancer Research Academy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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