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

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dc.contributor.author Chaudhuri, Aiswarya
dc.contributor.author Kumar, Dulla Naveen
dc.contributor.author Dehari, Deepa
dc.contributor.author Singh, Sanjay
dc.contributor.author Kumar, Pradeep
dc.contributor.author Bolla, Pradeep Kumar
dc.contributor.author Kumar, Dinesh
dc.contributor.author Agrawal, Ashish Kumar
dc.date.accessioned 2023-04-21T07:11:28Z
dc.date.available 2023-04-21T07:11:28Z
dc.date.issued 2022-05
dc.identifier.issn 14248247
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/2177
dc.description This paper is submitted by the author of IIT (BHU), Varanasi en_US
dc.description.abstract Triplenegative 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.sponsorship The 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.language.iso en en_US
dc.publisher MDPI en_US
dc.relation.ispartofseries Pharmaceuticals;Article number 542
dc.subject 8 [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; vorinostat en_US
dc.subject adjuvant 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 metastasis en_US
dc.title Emergence of Nanotechnology as a Powerful Cavalry against Triple-Negative Breast Cancer (TNBC) en_US
dc.type Article en_US


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