Year: 2020
Type: review
Abstract: The current pandemic (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a global health challenge with active development of antiviral drugs and vaccines seeking to reduce its significant disease burden. Early reports have confirmed that transmembrane serine protease 2 (TMPRSS2) and angiotensin converting enzyme 2 (ACE2) are critical targets of SARS-CoV-2 that facilitate viral entry into host cells. TMPRSS2 and ACE2 are expressed in multiple human tissues beyond the lung including the testes where predisposition to SARS-CoV-2 infection may exist. TMPRSS2 is an androgen-responsive gene and its fusion represents one of the most frequent alterations in prostate cancer. Androgen suppression by androgen deprivation therapy and androgen receptor signaling inhibitors form the foundation of prostate cancer treatment. In this review, we highlight the growing evidence in support of androgen regulation of TMPRSS2 and ACE2 and the potential clinical implications of using androgen suppression to downregulate TMPRSS2 to target SARS-CoV-2. We also discuss the future directions and controversies that need to be addressed in order to establish the viability of targeting TMPRSS2 and/or ACE2 through androgen signaling regulation for COVID-19 treatment, particularly its relevance in the context of prostate cancer management.
Source: Endocrine Related Cancer
DOI: 10.1530/erc-20-0165
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Awards: MECHANISMS OF GLUTAMINE METABOLISM IN LETHAL PROSTATE CANCER PROGRESSION AND RESISTANCE TO ANDROGEN SIGNALING BLOCKADE IN THE METASTATIC BONY, ROLE OF ANDROGEN DEPRIVATION-INDUCED GLUTAMINE IN PROSTATE CANCER METASTATIC PROGRESSION, G2727287603, G4119534169, G463559462, Determinants of Liver Metastasis, G7544365319
OpenAlex ID: W3033788509
