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dc.contributor.authorAydın, Dinçer
dc.contributor.authorBilici, Ahmet Erkan
dc.contributor.authorYavuzer, Dilek
dc.contributor.authorKefeli, Umut
dc.contributor.authorTan, A.
dc.contributor.authorErcelep, Özlem Balvan
dc.contributor.authorMert, Aslıhan Güven
dc.contributor.authorYüksel, Sinemis
dc.contributor.authorÖzçelik, Melike
dc.contributor.authorIşık, Deniz
dc.contributor.authorSürmeli, Heves
dc.contributor.authorOdabaşı, Hatice
dc.contributor.authorAliustaoǧlu, Mehmet
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:51:28Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:51:28Z
dc.date.issued2015en_US
dc.identifier.citationAydın, D., Bilici, A. E., Yavuzer, D., Kefeli, U., Tan, A.., Ercelep, Ö. B. ... Aliustaoǧlu, M. (2015). Prognostic significance of ADAM17 expression in patients with gastric cancer who underwent curative gastrectomy. Clinical and Translational Oncology, 17(8), 604-611. https://dx.doi.org/10.1007/s12094-015 1283-1en_US
dc.identifier.issn1699-048X
dc.identifier.issn1699-3055
dc.identifier.urihttps://dx.doi.org/10.1007/s12094-015-1283-1
dc.identifier.urihttps://hdl.handle.net/20.500.12511/2221
dc.descriptionWOS: 000358156300004en_US
dc.descriptionPubMed ID: 25786367en_US
dc.description.abstractA disintegrin and metalloproteinase (ADAM) 17 has been indicated to be an indispensable regulator of cellular events from proliferation to migration. Although prognostic importance of ADAM17 expression has been investigated in several tumours, its clinical utility as a useful prognostic molecular marker remains unclear in gastric cancer. In the current study, we evaluated the expression of ADAM17 and its prognostic significance in gastric cancer patients after curative gastrectomy. The prognostic significance of ADAM17 expression was analysed immunohistochemically in 156 patients with gastric cancer who had undergone curative gastrectomy, and the relationship between its expression and clinicopathological factors was also evaluated. High ADAM17 expression was detected in 79 patients (51 %), whereas low expression was found in 77 cases (49 %). There was significant correlation between gender, histology, lymph node metastasis, vascular invasion, the presence of recurrence and high ADAM17 expression. Recurrence in patients with high ADAM17 expression was significantly higher than that for patients with low ADAM17 expression (p = 0.032). The median disease-free survival (DFS) time for patients with tumours with high ADAM17 expression was worse than that of patients with tumours with low ADAM17 expression (16.6 vs. 44.2 months, p = 0.004). In addition, patients with low ADAM17 expression had a higher median overall survival (OS) (49.6 vs. 26.9 months, p = 0.019) compared to those with high ADAM17 expression. Multivariate analysis indicated that the rate of ADAM17 expression was an independent prognostic factor for DFS, in addition to the already known important clinicopathological prognostic indicator. But the prognostic importance of ADAM17 expression could not be proved by multivariate analysis for OS. The potential value of ADAM17 expression as a useful molecular marker in gastric cancer progression should be evaluated comprehensively; it may predict recurrence and poor prognosis in patients with gastric cancer after curative resection.en_US
dc.language.isoengen_US
dc.publisherSpringer-Verlagen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectADAM17en_US
dc.subjectGastric Canceren_US
dc.subjectPrognosisen_US
dc.titlePrognostic significance of ADAM17 expression in patients with gastric cancer who underwent curative gastrectomyen_US
dc.typearticleen_US
dc.relation.ispartofClinical and Translational Oncologyen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalıen_US
dc.identifier.volume17en_US
dc.identifier.issue8en_US
dc.identifier.startpage604en_US
dc.identifier.endpage611en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1007/s12094-015-1283-1en_US
dc.identifier.wosqualityQ3en_US
dc.identifier.scopusqualityQ2en_US


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