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dc.contributor.authorSusanto, Hendraen_US
dc.contributor.authorLiu, Ta-Yuen_US
dc.contributor.authorChen, Chang-Chiangen_US
dc.contributor.authorPurnomo, Jerry D. T.en_US
dc.contributor.authorChen, Shu-Fanen_US
dc.contributor.authorWang, Chih-Hongen_US
dc.date.accessioned2017-04-21T06:56:44Z-
dc.date.available2017-04-21T06:56:44Z-
dc.date.issued2016-07-05en_US
dc.identifier.issn1949-2553en_US
dc.identifier.urihttp://dx.doi.org/10.18632/oncotarget.9815en_US
dc.identifier.urihttp://hdl.handle.net/11536/132566-
dc.description.abstractLong-standing diabetes or glucose intolerance is recognized as a crucial event in the process of pancreatic cancer. Betatrophin, a novel liver-derived hormone, promotes beta-cell proliferation and improves glucose intolerance. However, the relationship between betatrophin and PDAC-associated diabetes is not fully understood. To evaluate the serum betatrophin levels in PDAC-associated diabetes, a total 105 Taiwanese subjects including 15 healthy subjects, and 12 patients having PDAC with normal glucose tolerance (PDAC-NGT), 12 patients having PC with impaired glucose tolerance (PDAC-IGT), and 66 patients having PC with diabetes mellitus (PDAC-DM) were enrolled for this study. Serum betatrophin and carbohydrate antigen 19-9 (CA19-9) levels were analyzed by enzyme-linked immunosorbent assay (ELISA). Compared to healthy subjects, PDAC patients had higher levels of betatrophin and CA19-9. Consistently, betatrophin protein was significantly expressed in pancreatic ductal of PDAC-associated DM patients using immunohistochemistry (IHC) method. Furthermore, multivariate regression analysis showed the betatrophin was significantly and positively independent with T category (beta = 0.605, P=0.010), serum albumin (beta = 0. 423, P=0.021), lipase (beta = 0.292, P=0.039), and blood urea nitrogen (BUN) (beta = 0.303, P=0.040). Further, the betatrophin was three folds of having PDAC-associated diabetes with the highest odds ratio [OR=3.39; 95% CI (1.20-9.57); P=0.021) and receiver operating characteristic (ROC) curve analysis showed that AUC value of betarophin was 0.853 which is slightly larger than AUC value of CA19-9 (0.792) in PDAC-DM patients. Interestingly, AUC value of betarophin plus CA19-9 was 0.988 in PDAC-DM patients. Therefore, betatrophin combined CA19-9 may serve as a potential biomarker for PDAC-associated diabetes.en_US
dc.language.isoen_USen_US
dc.subjectbetatrophinen_US
dc.subjectdiabetesen_US
dc.subjectinsulin resistanceen_US
dc.subjectglucose intoleranceen_US
dc.subjectpancreatic canceren_US
dc.titleIncreased serum levels of betatrophin in pancreatic cancer-associated diabetesen_US
dc.identifier.doi10.18632/oncotarget.9815en_US
dc.identifier.journalONCOTARGETen_US
dc.citation.volume7en_US
dc.citation.issue27en_US
dc.citation.spage42330en_US
dc.citation.epage42339en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department統計學研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitute of Statisticsen_US
dc.identifier.wosnumberWOS:000380942600108en_US
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