To study the involvement of DNA mismatch repair genes in non-small cell lung cancer, matched normal and tumoral DNA samples from 31 patients were analyzed for both LOH and microsatellite instability with 34 markers at or linked to hMLH1 (3p21), hMSH2 (2p16), hMSH3 (5q11-q13), hMSH6 (2p16), hPMS1 (2q
Expression of mismatch repair proteins, hMLH1/hMSH2, in non-small cell lung cancer tissues and its clinical significance
โ Scribed by Hidenori Kouso; Ichiro Yoshino; Naoko Miura; Tomoyoshi Takenaka; Taro Ohba; Tomofumi Yohena; Atsushi Osoegawa; Fumihiro Shoji; Yoshihiko Maehara
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 243 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0022-4790
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โฆ Synopsis
Abstract
Background
hMLH1 and hMSH2 have been implicated to be involved in the DNA mismatch repair (MMR) system. The purpose of this study is to investigate the expression of hMLH1 and hMSH2 DNA MMR proteins in nonโsmall cell lung cancer (NSCLC) tissue and to elucidate their clinical significance.
Methods
The hMLH1 and hMSH2 protein expression was evaluated by immunohistochemistry for a consecutive series of 113 NSCLC patients. The expressions of each protein were examined for an association with the clinicopathological variables, including genetic alterations analyzed by high resolution fluorescent microsatellite analysis.
Results
Regarding the hMLH1 expression, the MSIโpositive patients showed significantly lower scores than the MSIโnegative patients. For hMSH2 expression, the patients with a 20 or higher packโyear index (PYI) showed significantly higher scores than the patients with a PYI less than 20. The expression status of proteins did not affect both the disease free and overall survival of the patients. No significant correlation was observed among the scores for the proteins.
Conclusions
The expressions of hMLH1 and hMSH2 are independently regulated and play different roles in NSCLC. The genetic instability is possibly due to the reduced expression of hMLH1 protein, and hMSH2 expression is associated with smoking status. J. Surg. Oncol. 2008;98:377โ383. ยฉ 2008 WileyโLiss, Inc.
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