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Clinicopathological Significance of Large Tumor Suppressor (LATS) Expression in Gastric Cancer

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Abstract
PURPOSE: The aims of this study were to evaluate the expression of the large tumor suppressor (LATS) genes LATS1 and LATS2 by immunohistochemical staining of gastric cancer, and to evaluate the clinicopathological significance of LATS expression and its correlation with overall survival (OS). MATERIALS AND METHODS: LATS1 and LATS2 expression in a tissue microarray was detected by immunohistochemistry, using 264 gastric cancer specimens surgically resected between July 2006 and December 2009. RESULTS: Low expression of LATS1 was significantly associated with more advanced American Joint Committee on Cancer (AJCC) stage (P=0.001) and T stage (P=0.032), lymph node (LN) metastasis (P=0.040), perineural invasion (P=0.042), poor histologic grade (P=0.007), and diffuse-type histology by the Lauren classification (P=0.033). Low expression of LATS2 was significantly correlated with older age (≥65, P=0.027), more advanced AJCC stage (P=0.001) and T stage (P=0.001), LN metastasis (P=0.004), perineural invasion (P=0.004), poor histologic grade (P<0.001), and diffuse-type histology by the Lauren classification (P<0.001). Kaplan-Meier survival analysis revealed significantly poor OS rates in the groups with low LATS1 (P=0.037) and LATS2 (P=0.037) expression. CONCLUSIONS: Expression of LATS1 or LATS2 is a significant marker for a good prognosis in patients with gastric cancer.
All Author(s)
M. W. Son ; G. J. Song ; S. H. Jang ; S. A. Hong ; M. H. Oh ; J. H. Lee ; M. J. Baek ; M. S. Lee
Intsitutional Author(s)
손명원; 송금종; 장시형; 오미혜; 이지혜_병리과; 백무준; 이문수
Issued Date
2017
Type
Article
Keyword
Stomach neoplasms; Tumor suppressor genes; LATS1 protein, human; LATS2 protein, human
Publisher
대한위암학회
The Korean Gastric Cancer Association
ISSN
2093-582X ; 1598-1320
Citation Title
Journal of Gastric Cancer
Citation Volume
17
Citation Number
4
Citation Start Page
363
Citation End Page
373
Language(ISO)
eng
DOI
10.5230/jgc.2017.17.e41
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/3876
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