460 89

Full metadata record

DC FieldValueLanguage
dc.contributor.author민경환-
dc.date.accessioned2019-12-04T06:15:39Z-
dc.date.available2019-12-04T06:15:39Z-
dc.date.issued2018-01-
dc.identifier.citationJOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE, v. 52, no. 1, page. 37-44en_US
dc.identifier.issn2383-7837-
dc.identifier.issn2383-7845-
dc.identifier.urihttps://www.jpatholtm.org/journal/view.php?doi=10.4132/jptm.2017.10.20-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/117270-
dc.description.abstractBackground: Smad4 and PTEN are prognostic indicators for various tumor types. Smad4 regulates tumor suppression, whereas PTEN inhibits cell proliferation. We analyzed and compared the performance of Smad4 and PTEN for predicting the prognosis of patients with colorectal adenocarcinoma. Methods: Combined expression patterns based on Smad4+/- and PTEN+/- status were evaluated by immunostaining using a tissue microarray of colorectal adenocarcinoma. The relationships between the protein expression and clinicopathological variables were analyzed. Results: Smad4-/PTEN- status was most frequently observed in metastatic adenocarcinoma, followed by primary adenocarcinoma and tubular adenoma (p < .001). When Smad4-/PTEN- and Smad4+/PTEN+ groups were compared, Smad4-/PTEN- status was associated with high N stage (p = .018) and defective mismatch repair proteins (p = .006). Significant differences in disease-free survival and overall survival were observed among the three groups (Smad4+/PTEN+, Smad4-/PTEN+ or Smad4+/PTEN-, and Smad4-/PTEN-) (all p < .05). Conclusions: Concurrent loss of Smad4 and PTEN may lead to more aggressive disease and poor prognosis in patients with colorectal adenocarcinoma compared to the loss of Smad4 or PTEN alone.en_US
dc.language.isoen_USen_US
dc.publisherKOREAN SOC PATHOLOGISTSen_US
dc.subjectSmad4en_US
dc.subjectPTENen_US
dc.subjectPrognosisen_US
dc.subjectColon neoplasmsen_US
dc.subjectHumansen_US
dc.titleThe Smad4/PTEN Expression Pattern Predicts Clinical Outcomes in Colorectal Adenocarcinomaen_US
dc.typeArticleen_US
dc.relation.no1-
dc.relation.volume52-
dc.identifier.doi10.4132/jptm.2017.10.20-
dc.relation.page37-44-
dc.relation.journalJournal of Pathology and Translational Medicine-
dc.contributor.googleauthorChung, Yumin-
dc.contributor.googleauthorWi, Young Chan-
dc.contributor.googleauthorKim, Yeseul-
dc.contributor.googleauthorBang, Seong Sik-
dc.contributor.googleauthorYang, Jung-Ho-
dc.contributor.googleauthorJang, Kiseok-
dc.contributor.googleauthorMin, Kyueng-Whan-
dc.contributor.googleauthorPaik, Seung Sam-
dc.relation.code2018033969-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidkyueng-


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE