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dc.contributor.authorBassullu, Nuray
dc.contributor.authorTurkmen, Ilknur
dc.contributor.authorDayangac, Murat
dc.contributor.authorKorkmaz, Pinar Yagiz
dc.contributor.authorYasar, Reyhan
dc.contributor.authorAkyildiz, Murat
dc.contributor.authorDogusoy, Gulen Bulbul
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T16:03:28Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T16:03:28Z
dc.date.issued2012
dc.identifier.issn1735-143X
dc.identifier.issn1735-3408
dc.identifier.urihttps://dx.doi.org/10.5812/hepatmon.7492
dc.identifier.urihttp://hdl.handle.net/11446/3093
dc.descriptionWOS: 000314117000013en_US
dc.descriptionPubMed ID: 23162604en_US
dc.description.abstractBackground: Hepatocellular carcinoma (HCC) is the fifth most common fatal cancer and an important healthcare problem worldwide. There are many studies describing the prognostic and predictive effects of epidermal growth factor receptor 2 (c-erb-B2) and epidermal growth factor receptor 1 (EGFR), transmembrane tyrosine kinases that influence cell growth and proliferation in many tumors. Objectives: The current study aimed to investigate the expression levels of c-erb-B2, EGFR, PTEN, mTOR, PI3K, p27, and ERCC1 in hepatocellular carcinoma (HCC) and their correlation with other clinicopathologic features. Patients and Methods: Fifty HCC cases were stained immunohistochemically with these markers. Correlations between the markers and clinicopathologic characteristics and survival rates were analyzed. Results: No membranous c-erb-B2 staining was seen, whereas cytoplasmic positivity was present in 92% of HCC samples, membranous EGFR was observed in 40%, PI3K was found in all samples, and mTOR was seen in 30%, whereas reduced or absent PTEN expression was observed in 56% of samples and loss of p27 was seen in 92% of the cases. c-erb-B2 and mTOR overexpression, as well as reduced expression of p27, all correlated with multiple tumors (P = 0.041, P < 0.001, and P < 0.001, respectively). P27 loss, and mTOR and EGFR positivity were significantly correlated with AFP (P = 0.047, P = 0.004, and P = 0.008, respectively). Angiolymphatic invasion was more commonly seen in EGFR- and ERCC1-positive cases (P = 0.003 and P = 0.005). EGFR was also correlated with histological grade (P = 0.039). No significant correlations were found among PTEN, PI3K, and the clinicopathological parameters. Disease-free or overall survival rates showed significant differences among therapy modalities, AFP levels, angiolymphatic or lymph node invasions, and ERCC1 and p27 expression levels (P < 0.05). Conclusions: c-erb-B2, EGFR, mTOR, ERCC1 overexpression levels, and loss of p27 may play roles in hepatocarcinogenesis and may be significant predictors of aggressive tumor behavior. These markers were found to be correlated with certain clinicopathologic features, therapy modalities, and survival rates in the current study. These findings may help in planning new, targeted treatment strategies. Published by Kowsar Corp, 2012. cc 3.0.en_US
dc.description.sponsorshipNational Liver Transplantation Societyen_US
dc.description.sponsorshipThis study was supported by National Liver Transplantation Society. This study was partially accepted to be presented as a poster at 24th European Congress of Pathology in Prague, September 08-12, 2012.en_US
dc.language.isoengen_US
dc.publisherKOWSAR PUBLen_US
dc.identifier.doi10.5812/hepatmon.7492en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCarcinomaen_US
dc.subjectHepatocellularen_US
dc.subjectImmunohistochemistryen_US
dc.titleThe Predictive and Prognostic Significance of c-erb-B2, EGFR, PTEN, mTOR, PI3K, p27, and ERCC1 Expression in Hepatocellular Carcinomaen_US
dc.typearticleen_US
dc.relation.journalHEPATITIS MONTHLYen_US
dc.departmentDBÜen_US
dc.identifier.issue10en_US
dc.identifier.volume12en_US
dc.contributor.authorID0000-0002-1240-7233en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Bassullu, Nuray -- Turkmen, Ilknur] Istanbul Bilim Univ, Fac Med, Dept Pathol, Istanbul, Turkey -- [Dayangac, Murat] Florence Nigthingale Hosp, Dept Gen Surg, Istanbul, Turkey -- [Korkmaz, Pinar Yagiz -- Yasar, Reyhan -- Dogusoy, Gulen Bulbul] Florence Nigthingale Hosp, Dept Pathol, Istanbul, Turkey -- [Akyildiz, Murat] Istanbul Bilim Univ, Fac Med, Dept Gastroenterol, Istanbul, Turkey -- [Yaprak, Onur -- Tokat, Yaman -- Yuzer, Yildiray] Florence Nigthingale Hosp, Dept Gen Surg, Istanbul, Turkeyen_US


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