PMID- 33632295 OWN - NLM STAT- MEDLINE DCOM- 20210304 LR - 20240331 IS - 1757-2215 (Electronic) IS - 1757-2215 (Linking) VI - 14 IP - 1 DP - 2021 Feb 25 TI - Comorbidities and inflammation associated with ovarian cancer and its influence on SARS-CoV-2 infection. PG - 39 LID - 10.1186/s13048-021-00787-z [doi] LID - 39 AB - Coronavirus disease 2019 (COVID-19) caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) worldwide is a major public health concern. Cancer patients are considered a vulnerable population to SARS-CoV-2 infection and may develop several COVID-19 symptoms. The heightened immunocompromised state, prolonged chronic pro-inflammatory milieu coupled with comorbid conditions are shared in both disease conditions and may influence patient outcome. Although ovarian cancer (OC) and COVID-19 are diseases of entirely different primary organs, both diseases share similar molecular and cellular characteristics in their microenvironment suggesting a potential cooperativity leading to poor outcome. In COVID-19 related cases, hospitalizations and deaths worldwide are lower in women than in males; however, comorbidities associated with OC may increase the COVID-19 risk in women. The women at the age of 50-60 years are at greater risk of developing OC as well as SARS-CoV-2 infection. Increased levels of gonadotropin and androgen, dysregulated renin-angiotensin-aldosterone system (RAAS), hyper-coagulation and chronic inflammation are common conditions observed among OC and severe cases of COVID-19. The upregulation of common inflammatory cytokines and chemokines such as tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-1beta, IL-2, IL-6, IL-10, interferon-gamma-inducible protein 10 (IP-10), granulocyte colony-stimulating factor (G-CSF), monocyte chemoattractant protein-1 (MCP-1), macrophage colony-stimulating factor (M-CSF), among others in the sera of COVID-19 and OC subjects suggests potentially similar mechanism(s) involved in the hyper-inflammatory condition observed in both disease states. Thus, it is conceivable that the pathogenesis of OC may significantly contribute to the potential infection by SARS-CoV-2. Our understanding of the influence and mechanisms of SARS-CoV-2 infection on OC is at an early stage and in this article, we review the underlying pathogenesis presented by various comorbidities of OC and correlate their influence on SARS-CoV-2 infection. FAU - Chaudhari, Sima AU - Chaudhari S AD - Department of Cell and Molecular Biology, Manipal School of Life Science, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India. FAU - Dey Pereira, Satyajit AU - Dey Pereira S AD - Department of Cell and Molecular Biology, Manipal School of Life Science, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India. FAU - Asare-Warehene, Meshach AU - Asare-Warehene M AD - Chronic Disease Program, Ottawa Hospital Research Institute and Department of Obstetrics & Gynecology and Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, K1N 6N5, Canada. FAU - Naha, Ritam AU - Naha R AD - Department of Cell and Molecular Biology, Manipal School of Life Science, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India. FAU - Kabekkodu, Shama Prasada AU - Kabekkodu SP AD - Department of Cell and Molecular Biology, Manipal School of Life Science, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India. FAU - Tsang, Benjamin K AU - Tsang BK AD - Chronic Disease Program, Ottawa Hospital Research Institute and Department of Obstetrics & Gynecology and Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, K1N 6N5, Canada. FAU - Satyamoorthy, Kapaettu AU - Satyamoorthy K AUID- ORCID: 0000-0002-2368-5490 AD - Department of Cell and Molecular Biology, Manipal School of Life Science, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India. ksatyamoorthy@manipal.edu. LA - eng PT - Journal Article PT - Review DEP - 20210225 PL - England TA - J Ovarian Res JT - Journal of ovarian research JID - 101474849 RN - 0 (Cytokines) SB - IM MH - COVID-19/*epidemiology/*etiology MH - Comorbidity MH - Cytokines/metabolism MH - Female MH - Humans MH - Inflammation/*epidemiology/virology MH - Middle Aged MH - Ovarian Neoplasms/*epidemiology/*pathology MH - Renin-Angiotensin System/physiology MH - Tumor Microenvironment PMC - PMC7906086 OTO - NOTNLM OT - Hormones OT - Inflammation OT - Ovarian cancer OT - SARS-CoV-2 OT - risk factor COIS- The authors declare that they have no competing interests EDAT- 2021/02/27 06:00 MHDA- 2021/03/05 06:00 PMCR- 2021/02/25 CRDT- 2021/02/26 05:39 PHST- 2020/11/21 00:00 [received] PHST- 2021/02/09 00:00 [accepted] PHST- 2021/02/26 05:39 [entrez] PHST- 2021/02/27 06:00 [pubmed] PHST- 2021/03/05 06:00 [medline] PHST- 2021/02/25 00:00 [pmc-release] AID - 10.1186/s13048-021-00787-z [pii] AID - 787 [pii] AID - 10.1186/s13048-021-00787-z [doi] PST - epublish SO - J Ovarian Res. 2021 Feb 25;14(1):39. doi: 10.1186/s13048-021-00787-z.