Literature DB >> 12171885

Clinicopathological significance of galectin-3 expression in ductal adenocarcinoma of the pancreas.

Takeshi Shimamura1, Michiie Sakamoto, Yoshinori Ino, Kazuaki Shimada, Tomoo Kosuge, Yasuto Sato, Katsuaki Tanaka, Hisahiko Sekihara, Setsuo Hirohashi.   

Abstract

PURPOSE: Galectin-3, a member of the beta-galactoside-binding lectin family, has multiple biological functions including cell-cell interactions and cell-extracellular matrix adhesion, cellular proliferation, cellular differentiation, and apoptosis. The aim of this study was to determine the relationship of galectin-3 expression to clinicopathological findings and patient prognosis in ductal adenocarcinoma of the pancreas. EXPERIMENTAL
DESIGN: We examined galectin-3 expression in 104 surgically resected pancreatic ductal adenocarcinoma cases with stages I through IV using immunohistochemistry and investigated the relationship of it to overall survival.
RESULTS: Patients were divided into two groups: a low expression group, where <60% of tumor cells were positive; and a high expression group, where > or =60% of tumor cells were positive. Cases in the low expression group had a significant tendency to be at later stages, to have distant metastasis, and to have less differentiated tumors, compared with cases in the high expression group (P = 0.001 for stage, P = 0.001 for metastasis, and P = 0.006 for differentiation). Postoperative overall survival was worse in the low galectin-3 expression group than in the high galectin-3 expression group (P = 0.004). Multivariate analysis showed that the risk ratio of prognosis was 2.06 among patients in the low galectin-3 expression group compared with the high galectin-3 expression group (P = 0.006).
CONCLUSIONS: Decreased expression of galectin-3 was associated with advanced stage, tumor de-differentiation, and metastasis in ductal adenocarcinoma of the pancreas. Galectin-3 expression might be a useful prognostic marker for survival in ductal adenocarcinoma of the pancreas.

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Year:  2002        PMID: 12171885

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  23 in total

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2.  Novel INTeraction of MUC4 and galectin: potential pathobiological implications for metastasis in lethal pancreatic cancer.

Authors:  Shantibhusan Senapati; Pallavi Chaturvedi; William G Chaney; Subhankar Chakraborty; Vinayaga S Gnanapragassam; Aaron R Sasson; Surinder K Batra
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4.  Transient gene silencing of galectin-3 suppresses pancreatic cancer cell migration and invasion through degradation of β-catenin.

Authors:  Tsutomu Kobayashi; Tatsuo Shimura; Toshiki Yajima; Norio Kubo; Kenichiro Araki; Soichi Tsutsumi; Hideki Suzuki; Hiroyuki Kuwano; Avraham Raz
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Authors:  Matthias M Gaida; Sylvia T Bach; Frank Günther; Billur Baseras; Darjus F Tschaharganeh; Thilo Welsch; Klaus Felix; Frank Bergmann; Gertrud M Hänsch; Moritz N Wente
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7.  Targeted disruption of the galectin-3 gene results in decreased susceptibility to NNK-induced lung tumorigenesis: an oligonucleotide microarray study.

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8.  Loss of galectin-3 expression correlates with clear cell renal carcinoma progression and reduced survival.

Authors:  Axel S Merseburger; Mario W Kramer; Jörg Hennenlotter; Jürgen Serth; Stephan Kruck; Alfredo Gracia; Arnulf Stenzl; Markus A Kuczyk
Journal:  World J Urol       Date:  2008-07-02       Impact factor: 4.226

9.  Novel immunohistochemical marker, integrin α(V)β(3), for BOP-induced early lesions in hamster pancreatic ductal carcinogenesis.

Authors:  Tsukasa Kitahashi; Mitsuyoshi Yoshimoto; Toshio Imai
Journal:  Oncol Lett       Date:  2011-01-21       Impact factor: 2.967

10.  Clinicopathological and prognostic significance of myofibrillogenesis regulator-1 protein expression in pancreatic ductal adenocarcinoma.

Authors:  Chang-Yong Zhao; Zi-Jian Guo; Sai-Min Dai; Yong Zhang; Jun-Jing Zhou
Journal:  Tumour Biol       Date:  2013-05-22
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