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dc.contributor.authorArslan, A.I.
dc.contributor.authorKarabağ, S.
dc.contributor.authorAkgül, Murat
dc.date.accessioned2023-04-20T08:04:16Z
dc.date.available2023-04-20T08:04:16Z
dc.date.issued2022
dc.identifier.issn0974-5130
dc.identifier.urihttps://doi.org/10.4103/ijpm.ijpm_537_21
dc.identifier.urihttps://hdl.handle.net/20.500.11776/11060
dc.description.abstractPurpose: The present study aims to identify basaloid and luminal molecular groups and the p53-like sub-group, which is a sub-group of the luminal group, using a specific immunohistochemical panel and investigate human epithelial growth factor receptor 2 (HER2)/Neu and Fascin expression in these groups to analyze their relationship with clinicopathological features and prognosis in a cohort of cases with muscle-invasive urothelial bladder carcinoma (MIBC). Material and Methods: An immunohistochemical panel that included GATA-3, CK20, CD44, and CK5/6 was used to identify molecular sub-groups based on expression in 44 cases of MIBC. HER2/Neu and Fascin expression in basal, luminal, and p53-like groups and the relationship with clinicopathological features and prognosis were investigated. Results: The distribution of the molecular sub-groups determined by immunohistochemistry was as follows: 23 luminal cases (52.3%), 16 basal cases (36.4%), and 5 (11.4%) p53-like cases. There was a statistically significant difference in tumor size across the groups, with the greatest size in the p53-like group (p = 0.001). A statistically significant difference was observed in HER2/Neu expression between the molecular sub-groups (p = 0.017). Comparison of survival and HER2/Neu scores revealed shorter survival in patients with an HER2/Neu score of 3 + compared to those with scores of 0, 1+, and 2+ (p = 0.109). Fascin immunoreactivity was more common in the p53-like and basal groups compared to the luminal group (p = 0.036). Conclusion: Despite the limited number of cases in the MIBC group, our results support that HER2/Neu expression in the luminal sub-group and Fascin expression in basal and p53-like groups may be used as a negative prognostic marker. Multi-center studies that include large case series are warranted in this field.en_US
dc.language.isoengen_US
dc.publisherNLM (Medline)en_US
dc.identifier.doi10.4103/ijpm.ijpm_537_21
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBasalen_US
dc.subjectbladder canceren_US
dc.subjectfascinen_US
dc.subjectHER2/Neuen_US
dc.subjectimmunohistochemistryen_US
dc.subjectluminalen_US
dc.subjectp53-likeen_US
dc.subjectactin binding proteinen_US
dc.subjectcarrier proteinen_US
dc.subjectepidermal growth factor receptor 2en_US
dc.subjectfascinen_US
dc.subjectprotein p53en_US
dc.subjecttumor markeren_US
dc.subjectbladder tumoren_US
dc.subjectbreast tumoren_US
dc.subjectfemaleen_US
dc.subjectgeneticsen_US
dc.subjecthumanen_US
dc.subjectmetabolismen_US
dc.subjectmuscleen_US
dc.subjectpathologyen_US
dc.subjectphenotypeen_US
dc.subjectprognosisen_US
dc.subjectBiomarkers, Tumoren_US
dc.subjectBreast Neoplasmsen_US
dc.subjectCarrier Proteinsen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectMicrofilament Proteinsen_US
dc.subjectMusclesen_US
dc.subjectPhenotypeen_US
dc.subjectPrognosisen_US
dc.subjectReceptor, ErbB-2en_US
dc.subjectTumor Suppressor Protein p53en_US
dc.subjectUrinary Bladder Neoplasmsen_US
dc.titleEffect of HER2 and Fascin expression on muscle-invasive bladder cancers: Classification by basaloid and luminal phenotypesen_US
dc.typearticleen_US
dc.relation.ispartofIndian journal of pathology & microbiologyen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Üroloji Ana Bilim Dalıen_US
dc.identifier.volume65en_US
dc.identifier.issue3en_US
dc.identifier.startpage604en_US
dc.identifier.endpage609en_US
dc.institutionauthorArslan, A.I.
dc.institutionauthorKarabağ, S.
dc.institutionauthorAkgül, Murat
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57720962100
dc.authorscopusid56904163300
dc.authorscopusid57720994600
dc.identifier.scopus2-s2.0-85135202946en_US
dc.identifier.pmid35900488en_US


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