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LKB1 protein expression in neuroendocrine tumors of the lung
Author(s) -
Amin Randa Mahmoud Sobhi,
Hiroshima Kenzo,
Iyoda Akira,
Hoshi Kazuei,
Honma Koichi,
Kuroki Motoo,
Kokubo Takeshi,
Fujisawa Takehiko,
Miyagi Yohei,
Nakatani Yukio
Publication year - 2008
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1111/j.1440-1827.2007.02194.x
Subject(s) - immunohistochemistry , pathology , lung , neuroendocrine cell , carcinogenesis , small cell lung carcinoma , neuroendocrine tumors , biology , tumor suppressor gene , cancer research , gene expression , lung cancer , gene , medicine , small cell carcinoma , biochemistry
During a recent investigation of LKB1 gene abnormality in lung lesions, strong expression of LKB1 protein in normal neuroendocrine (NE) cells of the bronchial epithelium was found. Because LKB1 functions as a tumor suppressor gene, the question of whether alteration of LKB1 expression is related to the development of pulmonary NE tumors of various grades was investigated. LKB1 immunohistochemistry was examined in a total of 68 primary pulmonary NE tumors consisting of 30 specimens of small cell lung carcinoma (SCLC), 23 large cell neuroendocrine carcinomas (LCNEC), two atypical carcinoids, and 13 typical carcinoids. Loss or low expression (<20% immunoreactive cells) of LKB1 protein expression was more frequently observed in high‐grade NE tumors (SCLC and LCNEC; 45/53, 84.9%) than in typical and atypical carcinoids (3/15; 20%). The difference in LKB1 immunoreactivity between the high‐grade NE tumors and the carcinoid group was statistically significant ( P < 0.0001). In conclusion, marked reduction of LKB1 expression in high‐grade NE tumors of the lung suggests a possible role of LKB1 inactivation in its tumorigenesis. Although a few previous studies indicated rare genetic alterations of LKB1 in SCLC, further studies including analysis of other NE tumors and focusing on epigenetic abnormalities of LKB1 gene are warranted.