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pubmed-article:9951689pubmed:abstractTextIn this study the entire p53 complementary DNA has been sequenced in 20 non-small cell lung carcinomas (NSCLC) and the results correlated with chemosensitivity, immunohistochemistry and clinical data. Ten patients had mutations in p53, 8 missense mutations and 2 nonsense mutations. The method discovered two mutations never described previously and two other mutations that have never been described before in connection with NSCLC tumours. Chemosensitivity data, according to a short-term assay (FMCA), indicated that tumours with p53 mutation were more resistant to cisplatin and cyclophosphamide. Immunohistochemical studied demonstrated a 70% concordance between over-expression of p53 protein and mutation in p53. No conclusions or trends could be drawn from the immunohistochemical studies of Bcl-2 and Bax.lld:pubmed
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pubmed-article:9951689pubmed:articleTitleComplete sequence of p53 gene in 20 patients with lung cancer: comparison with chemosensitivity and immunohistochemistry.lld:pubmed
pubmed-article:9951689pubmed:affiliationDepartment of Oncology, Uppsala Akademiska Hospital, Uppsala University, Sweden.lld:pubmed
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