کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10911646 | 1088386 | 2005 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A lack of prognostic significance regarding ÎNp63 immunoreactivity in lung cancer
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
تحقیقات سرطان
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چکیده انگلیسی
ÎNp63 is an isoform of the p53 homologue p63, which lacks an amino-terminal transactivation domain and antagonizes the induction of the gene expression by Îp63. The aim of this study was to detect the ÎNp63 expression in lung cancer using immunohistochemical (IHC) staining, and to evaluate the relationship between theÎNp63 expression level and the prognosis based on resected lung cancer tissues specimens from the of patients. We used immunohistochemistry to analyze the protein expression of ÎNp63 in paraffin-embedded tumor samples from 161 well-characterized squamous cell carcinoma patients and compared the expression level of ÎNp63, clinical variables and the survival outcome. Seventy-seven patients (47.8%) showed positive staining for ÎNp63 in the nuclei of tumor cells. No significant difference was observed between the ÎNp63 expression and the gender, age at operation, pathologic stage, pathologic T status, and pathologic N status. Based on the actuarial survival method, Kaplan-Meier method, and the log-rank test, the ÎNp63 expression was not associated with survival for lung cancer. Differences in survival remained insignificant even after lung cancer patients were stratified according to stage or differentiation. The prognostic effects of ÎNp63 expression do not appear to act as an important prognostic indicator in lung cancer. Our findings do not support that immunocytochemical markers demonstrate a relevant prognostic role in lung cancer.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Lung Cancer - Volume 50, Issue 1, October 2005, Pages 67-73
Journal: Lung Cancer - Volume 50, Issue 1, October 2005, Pages 67-73
نویسندگان
Teruo Iwata, Hidetaka Uramoto, Kenji Sugio, Yoshihisa Fujino, Tsunehiro Oyama, Shoji Nakata, Kenji Ono, Masaru Morita, Kosei Yasumoto,