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Emergence of Nanotechnology as a Powerful Cavalry against Triple-Negative Breast Cancer (TNBC)

dc.contributor.authorChaudhuri, Aiswarya
dc.contributor.authorKumar, Dulla Naveen
dc.contributor.authorDehari, Deepa
dc.contributor.authorSingh, Sanjay
dc.contributor.authorKumar, Pradeep
dc.contributor.authorBolla, Pradeep Kumar
dc.contributor.authorKumar, Dinesh
dc.contributor.authorAgrawal, Ashish Kumar
dc.date.accessioned2023-04-21T07:11:28Z
dc.date.available2023-04-21T07:11:28Z
dc.date.issued2022-05
dc.descriptionThis paper is submitted by the author of IIT (BHU), Varanasien_US
dc.description.abstractTriplenegative breast cancer (TNBC) is considered one of the unmanageable types of breast cancer, involving devoid of estrogen, progesterone, and human epidermal growth factor receptor 2 (HER 2) receptors. Due to their ability of recurrence and metastasis, the management of TNBC remains a mainstay challenge, despite the advancements in cancer therapies. Conventional chemotherapy remains the only treatment regimen against TNBC and suffers several limitations such as low bioavailability, systemic toxicity, less targetability, and multidrug resistance. Although various targeted therapies have been introduced to manage the hardship of TNBC, they still experience certain limitations associated with the survival benefits. The current research thus aimed at developing and improving the strategies for effective therapy against TNBC. Such strategies involved the emergence of nanoparticles. Nanoparticles are designated as nanocavalries, loaded with various agents (drugs, genes, etc.) to battle the progression and metastasis of TNBC along with overcoming the limitations experienced by conventional chemotherapy and targeted therapy. This article documents the treatment regimens of TNBC along with their efficacy towards different subtypes of TNBC, and the various nanotechnologies employed to increase the therapeutic outcome of FDAapproved drug regimens.en_US
dc.description.sponsorshipThe authors are grateful to the Indian Institute of Technology (Banaras Hindu University), Varanasi for providing infrastructure facilities. Dulla Naveen Kumar is thankful to SERB for providing financial assistance in terms of JRF in one of the SERBsponsored projects (SRG/2019/000150).en_US
dc.identifier.issn14248247
dc.identifier.urihttps://idr-sdlib.iitbhu.ac.in/handle/123456789/2177
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofseriesPharmaceuticals;Article number 542
dc.subject8 [4 (1 aminocyclobutyl)phenyl] 9 phenyl 1,2,4 triazolo[3,4 f][1,6]naphthyridin 3(2h) one; abiraterone acetate; alpelisib; androgen receptor; anthracycline derivative; antibody drug conjugate; antineoplastic antimetabolite; apitolisib; asparaginase macrogol; atezolizumab; avelumab; azacitidine; bendamustine; bevacizumab; bicalutamide; bimiralisib; binimetinib; buparlisib; capecitabine; capivasertib; carbon nanotube; carboplatin; cetuximab; cisplatin; citral; cobimetinib; curcumin; cyclophosphamide; cytarabine; cytotoxic T lymphocyte antigen 4; dasatinib; daunorubicin; decitabine; dendrimer; diallyl disulfide; docetaxel; doxorubicin; durvalumab; edelfosine; enzalutamide; epidermal growth factor receptor; epirubicin; eribulin; erlotinib; etoposide; everolimus; floxuridine; fluoropyrimidine derivative; fluorouracil; galunisertib; gambogic acid; gamma secretase inhibitor; gedatolisib; gefitinib; gemcitabine; halofuginone; honokiol; idarubicin; immune checkpoint inhibitor; ipatasertib; irinotecan; ixabepilone; lapachol; liposome; lycopene; metal nanoparticle; methotrexate; mitomycin; mitoxantrone; mk 0752; n (6,7 dihydro 6 oxo 5h dibenz[b,d]azepin 7 yl) 2,2 dimethyl n' (2,2,3,3,3 pentafluoropropyl)propanediamide; nanocarrier; nanoparticle; niclosamide; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase 1; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor; niraparib; nirogacestat; olaparib; olinvacimab; omega 3 fatty acid; orteronel; paclitaxel; palbociclib; panitumumab; panobinostat; pembrolizumab; piperine; platinum complex; polymeric micelle; prednisone; programmed death 1 ligand 1; protein tyrosine kinase; quercetin; resveratrol; ridaforolimus; rucaparib; sacituzumab govitecan; saracatinib; selumetinib; silver nanoparticle; sirolimus; small interfering RNA; solid lipid nanoparticle; somatomedin C receptor; talazoparib; taselisib; taxane derivative; teniposide; tetrahydrolipstatin; thymoquinone; unclassified drug; valrubicin; vandetanib; veliparib; vincristine; vinorelbine tartrate; vistusertib; vorinostaten_US
dc.subjectadjuvant therapy; Akt signaling; basal like breast cancer; brain metastasis; breast cancer; breast cancer recurrence; cancer incidence; cancer prognosis; cancer regression; cancer resistance; colon cancer; disease free survival; distant metastasis; drug bioavailability; drug delivery system; drug formulation; drug penetration; drug solubility; encapsulation; epithelial mesenchymal transition; gene expression profiling; hedgehog signaling; human; lung cancer; lung metastasis; lymphocytopenia; metastatic breast cancer; molecularly targeted therapy; monotherapy; nanoemulsion; nanomedicine; non-canonical Wnt signaling; nonhuman; Notch signaling; ovary cancer; overall survival; partial mastectomy; personalized medicine; progression free survival; Review; self emulsifying drug delivery system; TGF beta signaling; triple negative breast cancer; tumor invasion; tumor microenvironment; visceral metastasisen_US
dc.titleEmergence of Nanotechnology as a Powerful Cavalry against Triple-Negative Breast Cancer (TNBC)en_US
dc.typeArticleen_US

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