4.7 Article

Evaluation of HER-2/neu gene amplification and protein expression in non-small cell lung carcinomas

期刊

BRITISH JOURNAL OF CANCER
卷 86, 期 9, 页码 1449-1456

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6600286

关键词

lung cancer; HER-2/neu; oncogene overexpression; immunohistochemistry; FISH; gene amplification

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资金

  1. NCI NIH HHS [U01-CA 85070, U01 CA085070, P50 CA058187, 2P30-CA 46934, P30 CA046934, P01-CA 58187] Funding Source: Medline

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HER-2/neu gene amplification and cell surface overexpression are important factors in breast cancer for prognosis and prediction of sensitivity to anti-HER-2/neu monoclonal antibody therapy. In lung cancer, the clinical significance of HER-2/neu expression is currently under evaluation. We investigated 238 non-small lung carcinomas for HER-2/neu protein overexpression by immunchistochemistry using the HercepTest. We found 2+ or 3+ overexpression in 39 patients (16%), including 35%. in adenocarcinomas and 20% in large cell carcinomas, but only 1% of squamous cell carcinomas. Marked (3+) overexpression was uncommon (4%). The association between protein expression and gene copy number per cell, as determined by fluorescence in situ hybridisation assay, was Investigated in 5 1 of these NSCLC tumours. Twenty-seven tumours (53%) were negative by both tests. Marked (3+) protein expression and gene amplification were present in only 4% of samples. In 11 tumours (2156), gene gain was accompanied by chromosomal aneusomy and did not result in high protein levels while in 7 (14%) the score 2+ was associated with maximum number of signals per cell <9. The prognostic implication of HER-2/neu protein expression was studied in 187 surgically resected tumours. No statistical difference in survival was observed comparing patients with positive (2+/3+) and negative tumours (0/1+), although 3+ patients showed a tendency to shorter survival. The therapeutic implications of protein expression and gene amplification in lung cancer need to be examined in prospective clinical trials. (C) 2002 Cancer Research UK.

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