@Article{Yuan2013,
journal="Polish Journal of Pathology",
issn="1233-9687",
volume="64",
number="1",
year="2013",
title="Clinicopathological significance of DNA fragmentation factor 45 and thyroid transcription factor 1 expression in benign and malignant lesions of the gallbladder",
abstract="Gallbladder cancer (GBC) is one of the most aggressive tumors; we examined the expression level of DNA fragmentation factor 45 (DFF45) and thyroid transcription factor 1 (TTF-1) in benign and malignant lesions of the gallbladder by immunohistochemistry. The results were correlated with clinicopathological features and prognosis. DNA fragmentation factor 45 and TTF-1 expression was significantly higher in gallbladder adenocarcinomas than in the corresponding peritumoral tissues (χ 2  DFF45  = 6.92, χ 2  TTF-1  = 8.68, ps < 0.01), polyps (χ 2  DFF45  = 4.49, χ 2  TTF-1  = 5.35, ps < 0.05), and chronic cholecystitis (χ 2  DFF45  = 12.98, χ 2  TTF-1  = 17.74, ps < 0.01). Negative expression of DFF45 and TTF-1 was significantly associated with tumor differentiation, tumor mass, lymph node metastasis and invasion of adenocarcinomas (p < 0.05). Univariate Kaplan-Meier analysis showed that elevated expression levels of DFF45 and TTF-1 (p < 0.05) were closely associated with increased overall survival. In addition, the average survival time of patients with DFF45(+) TTF-1(+) tumors was significantly higher than those with DFF45(–) TTF-1(–) tumors (p < 0.05). Finally, multivariate Cox regression analysis showed that negative expression of DFF45 and TTF-1 was an independent prognostic predictor in gallbladder adenocarcinoma (p < 0.05). The expression of DFF45 and/or TTF-1 is closely related to the carcinogenesis, progression, clinical behavior and prognosis of gallbladder adenocarcinomas. DNA fragmentation factor 45 and TTF-1 could be progression-associated genes correlating with good prognosis in GBC.",
author="Yuan, Yuan
and Yang, Zhu-Lin
and Zou, Qiong
and Cao, Li-Fen
and Tan, Xing-Guo
and Jiang, Song
and Miao, Xiong-Ying",
pages="44--51",
doi="10.5114/pjp.2013.34603",
url="http://dx.doi.org/10.5114/pjp.2013.34603"
}