Multiple roles for basement membrane proteins in cancer progression and EMT

dc.authorscopusid57225897167
dc.authorscopusid57552626300
dc.authorscopusid57553332000
dc.authorscopusid55480940800
dc.authorscopusid57315858300
dc.authorscopusid57417573800
dc.authorscopusid57203059732
dc.contributor.authorBanerjee, Samarpita
dc.contributor.authorLo, Wen-Cheng
dc.contributor.authorMajumder, Payel
dc.contributor.authorRoy, Debleena
dc.contributor.authorGhorai, Mimosa
dc.contributor.authorShaikh, Nusrat K.
dc.contributor.authorGundamaraju, Rohit
dc.date.accessioned2022-09-04T10:27:03Z
dc.date.available2022-09-04T10:27:03Z
dc.date.issued2022
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.description.abstractMetastasis or the progression of malignancy poses a major challenge in cancer therapy and is the principal reason for increased mortality. The epithelial-mesenchymal transition (EMT) of the basement membrane (BM) allows cells of epithelial phenotype to transform into a mesenchymal-like (quasi-mesenchymal) phenotype and metastasize via the lymphovascular system through a metastatic cascade by intravasation and extravasation. This helps in the progression of carcinoma from the primary site to distant organs. Collagen, laminin, and integrin are the prime components of BM and help in tumor cell metastasis, which makes them ideal cancer drug targets. Further, recent studies have shown that collagen, laminin, and integrin can be used as a biomarker for metastatic cells. In this review, we have summarized the current knowledge of such therapeutics, which are either currently in preclinical or clinical stages and could be promising cancer therapeutics.Data availability: Not applicableen_US
dc.description.sponsorshipScientific Research at Majmaah University [R-2022-117]en_US
dc.description.sponsorshipDr. Niraj Kumar Jha is thankful to Sharda University for the infra-structure and facility. The author would like to thank Deanship of Sci-entific Research at Majmaah University for supporting this work under project number No. R-2022-117. The authors would like to acknowledge the support from their respective institutes throughout the review writing process.en_US
dc.identifier.doi10.1016/j.ejcb.2022.151220
dc.identifier.issn0171-9335
dc.identifier.issn1618-1298
dc.identifier.issue2en_US
dc.identifier.orcid0000-0002-6947-7582
dc.identifier.orcidKumar, Sanjay
dc.identifier.orcid0000-0001-6296-0291
dc.identifier.orcid0000-0002-8821-1720
dc.identifier.pmid35366585
dc.identifier.scopus2-s2.0-85127104865
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.ejcb.2022.151220
dc.identifier.urihttps://hdl.handle.net/20.500.12639/4709
dc.identifier.volume101en_US
dc.identifier.wosWOS:000807501400004
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorBursal, Ercan
dc.language.isoen
dc.publisherElsevier Gmbhen_US
dc.relation.ispartofEuropean Journal Of Cell Biologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBasement membrane; EMT; Metastasis; Collagen; Laminin; Integrinen_US
dc.subjectSquamous-Cell Carcinoma; Breast-Cancer; I Collagen; Colorectal-Cancer; Gene-Expression; Malignant Phenotype; Biological-Activity; Extracellular-Matrix; Promotes; Integrinen_US
dc.titleMultiple roles for basement membrane proteins in cancer progression and EMTen_US
dc.typeArticle

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