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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jha, Hem Chandra | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-17T15:30:58Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-17T15:30:58Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Parmar, H. S., Nayak, A., Gavel, P. K., Jha, H. C., Bhagwat, S., & Sharma, R. (2021). Cross talk between covid-19 and breast cancer. Current Cancer Drug Targets, 21(7), 575-600. doi:10.2174/1568009621666210216102236 | en_US |
dc.identifier.issn | 1568-0096 | - |
dc.identifier.other | EID(2-s2.0-85106960034) | - |
dc.identifier.uri | https://doi.org/10.2174/1568009621666210216102236 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/3898 | - |
dc.description.abstract | Cancer patients are more susceptible to COVID-19; however, the prevalence of COVID-19 in different types of cancer is still inconsistent and inconclusive. Here, we delineate the intricate relationship between breast cancer and COVID-19. Breast cancer and COVID-19 share the involvement of common comorbidities, hormonal signalling pathways, gender differences, renn-in-angiotensin system (RAS), angiotensin-converting enzyme-2 (ACE-2), transmembrane protease serine 2 (TMPRSS2) and dipeptidyl peptidase-IV (DPP-IV). We also shed light on the possible effects of therapeutic modalities of COVID-19 on breast cancer outcomes. Briefly, we conclude that breast cancer patients are more susceptible to COVID-19 in comparison with their normal counter-parts. Women are more resistant to the occurrence and severity of COVID-19. Increased expressions of ACE2 and TMPRSS2 are correlated with occurrence and severity of COVID-19, but higher expression of ACE2 and lower expression of TMPRSS2 are prognostic markers for overall disease free survival in breast cancer. The ACE2 inhibitors and ibuprofen therapies for COVID-19 treatment may aggravate the clinical condition of breast cancer patients through chemo-resistance and metastasis. Most of the available therapeutic modalities for COVID-19 were also found to ex-ert positive effects on breast cancer outcomes. Besides drugs in clinical trend, TMPRSS2 inhibi-tors, estrogen supplementation, androgen deprivation and DPP-IV inhibitors may also be used to treat breast cancer patients infected with SARS-CoV-2. However, drug-drug interactions suggest that some of the drugs used for the treatment of COVID-19 may modulate the drug metabolism of anticancer therapies which may lead to adverse drug reaction events. © 2021 Bentham Science Publishers. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Bentham Science Publishers | en_US |
dc.source | Current Cancer Drug Targets | en_US |
dc.subject | androgen | en_US |
dc.subject | angiotensin | en_US |
dc.subject | angiotensin converting enzyme 2 | en_US |
dc.subject | dipeptidyl peptidase IV | en_US |
dc.subject | matrix metalloproteinase 16 | en_US |
dc.subject | reactive oxygen metabolite | en_US |
dc.subject | testosterone | en_US |
dc.subject | transmembrane protease serine 2 | en_US |
dc.subject | ACE2 protein, human | en_US |
dc.subject | antivirus agent | en_US |
dc.subject | serine proteinase | en_US |
dc.subject | sex hormone | en_US |
dc.subject | TMPRSS2 protein, human | en_US |
dc.subject | Article | en_US |
dc.subject | breast cancer | en_US |
dc.subject | cancer patient | en_US |
dc.subject | cancer prognosis | en_US |
dc.subject | cancer survival | en_US |
dc.subject | coronavirus disease 2019 | en_US |
dc.subject | disease free survival | en_US |
dc.subject | DNA damage | en_US |
dc.subject | drug interaction | en_US |
dc.subject | endoplasmic reticulum stress | en_US |
dc.subject | epithelial mesenchymal transition | en_US |
dc.subject | gene expression | en_US |
dc.subject | glucose blood level | en_US |
dc.subject | gonadectomy | en_US |
dc.subject | hormone substitution | en_US |
dc.subject | hospitalization | en_US |
dc.subject | human | en_US |
dc.subject | hydrogen bond | en_US |
dc.subject | immune response | en_US |
dc.subject | mastectomy | en_US |
dc.subject | mitochondrial biogenesis | en_US |
dc.subject | molecular docking | en_US |
dc.subject | nonhuman | en_US |
dc.subject | overall survival | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | prevalence | en_US |
dc.subject | protein expression | en_US |
dc.subject | protein synthesis | en_US |
dc.subject | renin angiotensin aldosterone system | en_US |
dc.subject | risk factor | en_US |
dc.subject | Severe acute respiratory syndrome coronavirus 2 | en_US |
dc.subject | signal transduction | en_US |
dc.subject | tumor growth | en_US |
dc.subject | tumor volume | en_US |
dc.subject | ubiquitination | en_US |
dc.subject | unfolded protein response | en_US |
dc.subject | upregulation | en_US |
dc.subject | vascular smooth muscle cell | en_US |
dc.subject | breast tumor | en_US |
dc.subject | comorbidity | en_US |
dc.subject | drug repositioning | en_US |
dc.subject | female | en_US |
dc.subject | genetics | en_US |
dc.subject | male | en_US |
dc.subject | metabolism | en_US |
dc.subject | mortality | en_US |
dc.subject | obesity | en_US |
dc.subject | Angiotensin-Converting Enzyme 2 | en_US |
dc.subject | Antiviral Agents | en_US |
dc.subject | Breast Neoplasms | en_US |
dc.subject | Comorbidity | en_US |
dc.subject | COVID-19 | en_US |
dc.subject | Drug Interactions | en_US |
dc.subject | Drug Repositioning | en_US |
dc.subject | Female | en_US |
dc.subject | Gonadal Steroid Hormones | en_US |
dc.subject | Humans | en_US |
dc.subject | Male | en_US |
dc.subject | Obesity | en_US |
dc.subject | Renin-Angiotensin System | en_US |
dc.subject | Serine Endopeptidases | en_US |
dc.title | Cross talk between covid-19 and breast cancer | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Biosciences and Biomedical Engineering |
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