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作 者:梁龙[1] 孔燕[1] 张虔男[1] 代杰[1] 马家芳 李怡倩 周琳 王薇[1] 郭军[1]
机构地区:[1]北京大学临床肿瘤学院、北京肿瘤医院暨北京市肿瘤防治研究所肾癌黑素瘤内科,恶性肿瘤发病机制及转化研究教育部重点实验室,北京100142
出 处:《肿瘤》2013年第7期604-609,共6页Tumor
基 金:国家自然科学基金资助项目(编号:81172196、81102068);北京市科学技术委员会科技新星资助项目(编号:2012035);北京市卫生局“215”高层次卫生技术人才培养资助专项经费(2011-02-25)
摘 要:目的:分析中国黑素瘤患者第10号染色体同源缺失性磷酸酶-张力蛋白(phosphatase and tensinhomologue deleted on chromosome10,PTEN)基因突变情况及其临床意义。方法:收集117例中国黑素瘤患者的肿瘤组织标本(42例为黏膜型,39例为肢端型,23例为慢性非日光损伤型,13例为慢性日光损伤型)。应用PCR扩增和基因测序方法检测PTEN基因1~9号外显子的突变情况。结果:117例黑素瘤患者的PTEN基因突变率为13.7%(16/117),其中黏膜型患者的突变率为16.7%(7/42),肢端型为15.4%(6/39),慢性非日光损伤型为8.7%(2/23),慢性日光损伤型为7.7%(1/13)。在肿瘤厚度≥4mm的患者中,PTEN野生型患者的总生存期明显长于突变型患者(χ2=4.237,P=0.04)。结论:本研究首次报道了中国黑素瘤患者中较高的PTEN基因突变率,提示检测PTEN基因突变情况有助于判断黑素瘤患者的预后。Objective: This study was designed to investigate the frequency of PTEN (phosphatase and tensin homologue deleted on chromosome 10) mutation in Chinese melanoma patients and explore its clinical significance. Methods: One hundred and seventeen melanoma specimens (42 mucosal melanomas, 39 acral melanomas, 23 non-chronic sun-induced damage melanomas, 13 chronic sun-induced damage melanomas) were collected and the mutation status in exons 1-9 of PTEN gene in genomic DNA were analyzed by PCR amplification and Sanger sequencing. Results: The frequency of PTEN mutation was 13.7% (16/117) in 117 melanoma specimens detected, and the frequencies of PTEN mutation in the mucosal, acral, non-chronic sun-induced damage and chronic sun-induced damage melanoma subtypes were 16.7% (7/42), 15.4% (6/39), 8.7% (2/23)and 7.7% (1/13), respectively. Patients whose tumor thickness equal to or more than 4 mm with wild type PTEN had a prolonged overall survival time as compared with that of the patients with PTEN mutation (χ2 = 4.237, P = 0.04). Conclusion: This study first reported that the frequency of PTEN mutation in Chinese melanoma patients, suggesting that PTEN mutation may be an independent prognostic factor for advanced melanoma patients.
关 键 词:黑素瘤 第10号染色体同源缺失性磷酸酶-张力蛋白 PTEN 基因突变 预后
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