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Tumor suppressor genes on frequently deleted chromosome 3p in nasopharyngeal carcinoma 被引量:7
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作者 Juan Chen Li Fu +3 位作者 Li-Yi Zhang Dora L. Kwong Li Yan Xin-Yuan Guan 《Chinese Journal of Cancer》 SCIE CAS CSCD 2012年第5期215-222,共8页
Nasopharyngeal carcinoma (NPC) is among the most common malignancies in southern China.Deletion of genomic DNA,which occurs during the complex pathogenesis process for NPC,represents a pivotal mechanism in the inactiv... Nasopharyngeal carcinoma (NPC) is among the most common malignancies in southern China.Deletion of genomic DNA,which occurs during the complex pathogenesis process for NPC,represents a pivotal mechanism in the inactivation of tumor suppressor genes (TSGs).In many circumstances,loss of TSGs can be detected as diagnostic and prognostic markers in cancer.The short arm of chromosome 3 (3p) is a frequently deleted chromosomal region in NPC,with 3p21.1-21.2 and 3p25.2-26.1 being the most frequently deleted minimal regions.In recent years,our research group and others have focused on the identification and characterization of novel target TSGs at 3p,such as RASSF1A,BLU,RBMS3,and CHL1,in the development and progression of NPC.In this review,we summarize recent findings of TSGs at 3p and discuss some of these genes in detail.A better understanding of TSGs at 3p will significantly improve our understanding of NPC pathogenesis,diagnosis,and treatment. 展开更多
关键词 3号染色体 抑癌基因 鼻咽癌 删除 全国人民代表大会 基因组DNA 肿瘤抑制基因 发病机制
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Detailed Deletion Mapping of Chromosome 9p21-22 in Nasopharyngeal Carcinoma
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作者 阳剑波 张晓梅 +6 位作者 邓龙文 谭国林 周鸣 曾朝阳 曹莉 沈守荣 李桂源 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 2000年第3期8-11,共4页
Objective: To further refine the extent of deletion on chromosome 9p21-22 in nasopharyngeal carcinoma (NPC) and provide evidence for discovering new tumor suppressor gene. Methods: Loss of heterozygosity (LOH) on chro... Objective: To further refine the extent of deletion on chromosome 9p21-22 in nasopharyngeal carcinoma (NPC) and provide evidence for discovering new tumor suppressor gene. Methods: Loss of heterozygosity (LOH) on chromosome 9p21-22 was analyzed in 25 paired blood and tumor samples by using 11 high-density microsatellite polymorphic markers. Results: 17 of 25 cases (68.0%) showed LOH at one or more loci. Higher frequencies of LOH were found at four loci: D9S161 (35.0%), D9S1678 (31.5%), D9S263 (33.3%) and D9S1853 (33.3%), where 6 cases had a contiguous stretch of allelic loss. Conclusion: The minimal common region of deletion might be defined between D9S161 and D9S1853 (estimated about 2.7 cM in extent) at 9p21.1, suggesting that inactivation of one or more tumor suppressor genes located in this region may be an important step in NPC. 展开更多
关键词 nasopharyngeal carcinoma Chromosome 9p21-22 Loss of heterozygosity tumor suppressor gene
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