Genetic alterations in early‐stage pulmonary large cell neuroendocrine carcinoma

BACKGROUND Small cell lung carcinoma (SCLC) and pulmonary large cell neuroendocrine carcinoma (LCNEC) are high‐grade malignant neuroendocrine tumors. Histologic differentiation between SCLC and LCNEC is difficult in some cases and to the authors' knowledge, genetic alterations associated with L...

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Veröffentlicht in:Cancer 2004-03, Vol.100 (6), p.1190-1198
Hauptverfasser: Hiroshima, Kenzo, Iyoda, Akira, Shibuya, Kiyoshi, Haga, Yukiko, Toyozaki, Tetsuya, Iizasa, Toshihiko, Nakayama, Toshinori, Fujisawa, Takehiko, Ohwada, Hidemi
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Sprache:eng
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Zusammenfassung:BACKGROUND Small cell lung carcinoma (SCLC) and pulmonary large cell neuroendocrine carcinoma (LCNEC) are high‐grade malignant neuroendocrine tumors. Histologic differentiation between SCLC and LCNEC is difficult in some cases and to the authors' knowledge, genetic alterations associated with LCNEC have not been identified. Therefore, the authors studied genetic alterations found in LCNEC and compared them with those of SCLC and classic large cell carcinoma (CLCC). METHODS Twenty‐two patients with UICC TNM Stage I LCNEC, 12 patients with Stage I CLCC, and 11 patients with SCLC with limited disease were studied. All tumors were resected completely. Loss of heterozygosity (LOH) of the tumor cells was detected using fluorescent primers. Methylation status of the p16 gene and expression of the p53 protein, retinoblastoma protein, and p16 protein were evaluated immunohistochemically. RESULTS LOH at TP53 and 13q14 was observed in most patients. The prevalence of LOH at D3S1295, D3S1234, and D5S407 was significantly higher in patients with LCNEC and SCLC than in patients with CLCC. The prevalence of LOH at D5S422 was higher in patients with CLCC and in patients with SCLC than in patients with LCNEC. Expression of the p16 protein was observed more frequently in SCLC than in CLCC or LCNEC. Hypermethylation of the p16 gene was observed more frequently in LCNEC than in SCLC. Patients with allelic losses at D3S1234 and D10S1686 had poorer prognoses compared with patients without allelic losses at these sites. CONCLUSIONS Genetic alterations of LCNEC were akin to those of SCLC. However, allelic losses at 5q and abnormalities in the p16 gene may differentiate LCNEC from SCLC. Cancer 2004. © 2004 American Cancer Society. Allelic losses at 3p occurred both in large cell neuroendocrine carcinoma (LCNEC) and small cell lung carcinoma (SCLC), but not in classic large cell carcinoma, at an early stage of carcinogenesis. The p16 gene abnormality occurred frequently in LCNEC, but not in SCLC.
ISSN:0008-543X
1097-0142
DOI:10.1002/cncr.20108