| Literature DB >> 33396563 |
Zhongyan Wang1, Megan Snyder2, Jessica E Kenison3, Kangkang Yang1, Brian Lara4, Emily Lydell1, Kawtar Bennani4, Olga Novikov5, Anthony Federico6, Stefano Monti6, David H Sherr1.
Abstract
For decades, the aryl hydrocarbon receptor (AHR) was studied for its role in environmental chemical toxicity i.e., as a quirk of nature and a mediator of unintended consequences of human pollution. During that period, it was not certain that the AHR had a "normal" physiological function. However, the ongoing accumulation of data from an ever-expanding variety of studies on cancer, cancer immunity, autoimmunity, organ development, and other areas bears witness to a staggering array of AHR-controlled normal and pathological activities. The objective of this review is to discuss how the AHR has gone from a likely contributor to genotoxic environmental carcinogen-induced cancer to a master regulator of malignant cell progression and cancer aggression. Particular focus is placed on the association between AHR activity and poor cancer outcomes, feedback loops that control chronic AHR activity in cancer, and the role of chronically active AHR in driving cancer cell invasion, migration, cancer stem cell characteristics, and survival.Entities:
Keywords: AHR; aryl hydrocarbon receptor; cancer; kynurenine pathway
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Year: 2020 PMID: 33396563 PMCID: PMC7795223 DOI: 10.3390/ijms22010387
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 6.208