Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3898
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dc.contributor.authorJha, Hem Chandraen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-17T15:30:58Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-17T15:30:58Z-
dc.date.issued2021-
dc.identifier.citationParmar, 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:10.2174/1568009621666210216102236en_US
dc.identifier.issn1568-0096-
dc.identifier.otherEID(2-s2.0-85106960034)-
dc.identifier.urihttps://doi.org/10.2174/1568009621666210216102236-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/3898-
dc.description.abstractCancer 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.isoenen_US
dc.publisherBentham Science Publishersen_US
dc.sourceCurrent Cancer Drug Targetsen_US
dc.subjectandrogenen_US
dc.subjectangiotensinen_US
dc.subjectangiotensin converting enzyme 2en_US
dc.subjectdipeptidyl peptidase IVen_US
dc.subjectmatrix metalloproteinase 16en_US
dc.subjectreactive oxygen metaboliteen_US
dc.subjecttestosteroneen_US
dc.subjecttransmembrane protease serine 2en_US
dc.subjectACE2 protein, humanen_US
dc.subjectantivirus agenten_US
dc.subjectserine proteinaseen_US
dc.subjectsex hormoneen_US
dc.subjectTMPRSS2 protein, humanen_US
dc.subjectArticleen_US
dc.subjectbreast canceren_US
dc.subjectcancer patienten_US
dc.subjectcancer prognosisen_US
dc.subjectcancer survivalen_US
dc.subjectcoronavirus disease 2019en_US
dc.subjectdisease free survivalen_US
dc.subjectDNA damageen_US
dc.subjectdrug interactionen_US
dc.subjectendoplasmic reticulum stressen_US
dc.subjectepithelial mesenchymal transitionen_US
dc.subjectgene expressionen_US
dc.subjectglucose blood levelen_US
dc.subjectgonadectomyen_US
dc.subjecthormone substitutionen_US
dc.subjecthospitalizationen_US
dc.subjecthumanen_US
dc.subjecthydrogen bonden_US
dc.subjectimmune responseen_US
dc.subjectmastectomyen_US
dc.subjectmitochondrial biogenesisen_US
dc.subjectmolecular dockingen_US
dc.subjectnonhumanen_US
dc.subjectoverall survivalen_US
dc.subjectoxidative stressen_US
dc.subjectprevalenceen_US
dc.subjectprotein expressionen_US
dc.subjectprotein synthesisen_US
dc.subjectrenin angiotensin aldosterone systemen_US
dc.subjectrisk factoren_US
dc.subjectSevere acute respiratory syndrome coronavirus 2en_US
dc.subjectsignal transductionen_US
dc.subjecttumor growthen_US
dc.subjecttumor volumeen_US
dc.subjectubiquitinationen_US
dc.subjectunfolded protein responseen_US
dc.subjectupregulationen_US
dc.subjectvascular smooth muscle cellen_US
dc.subjectbreast tumoren_US
dc.subjectcomorbidityen_US
dc.subjectdrug repositioningen_US
dc.subjectfemaleen_US
dc.subjectgeneticsen_US
dc.subjectmaleen_US
dc.subjectmetabolismen_US
dc.subjectmortalityen_US
dc.subjectobesityen_US
dc.subjectAngiotensin-Converting Enzyme 2en_US
dc.subjectAntiviral Agentsen_US
dc.subjectBreast Neoplasmsen_US
dc.subjectComorbidityen_US
dc.subjectCOVID-19en_US
dc.subjectDrug Interactionsen_US
dc.subjectDrug Repositioningen_US
dc.subjectFemaleen_US
dc.subjectGonadal Steroid Hormonesen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectObesityen_US
dc.subjectRenin-Angiotensin Systemen_US
dc.subjectSerine Endopeptidasesen_US
dc.titleCross talk between covid-19 and breast canceren_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Biosciences and Biomedical Engineering

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