首页> 外文期刊>Japanese Journal of Cancer Research >Mapping of target regions of allelic loss in primary breast cancers to 1-cM intervals on genomic contigs at 6q21 and 6q25.3.
【24h】

Mapping of target regions of allelic loss in primary breast cancers to 1-cM intervals on genomic contigs at 6q21 and 6q25.3.

机译:在6q21和6q25.3的基因组重叠群上,将原发性乳腺癌等位基因丢失的目标区域映射到1-cM区间。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Allelic losses on the long arm of human chromosome 6 are frequently observed in cancers of the ovary, prostate, and breast. To identify the locations of putative tumor suppressor genes on 6q, we examined 192 primary breast cancers for patterns of allelic loss at 16 polymorphic microsatellite loci distributed along this chromosome arm. Allelic losses at one or more loci were observed in 105 (55%) of the tumors examined. Detailed deletion mapping with appropriate yeast artificial chromosome (YAC) contigs identified two distinct commonly deleted regions; one was confined to a 1-cM interval at 6q21 flanked by D6S1040 and D6S262 and the other to a 1-cM interval at 6q25.3 flanked by D6S305 and D6S411. Allelic losses at 6q21 were more frequent in invasive solid tubular and scirrhous carcinomas than in tumors of less aggressive histologic types (P = 0.0006). Allelic loss at 6q25.3 was associated with loss of progesterone receptor (P = 0.0256). Our results suggest the presence of two tumor suppressor genes for breast cancer on 6q that are likely to be associated with tumor progression and / or loss of hormonal dependency.
机译:在卵巢癌,前列腺癌和乳腺癌中经常观察到人类6号染色体长臂上的等位基因缺失。为了确定推定的肿瘤抑制基因在6q上的位置,我们检查了192个原发性乳腺癌在沿着该染色体臂分布的16个多态微卫星基因座上的等位基因丢失模式。在所检查的105例肿瘤中(55%)观察到一个或多个基因座的等位基因缺失。用适当的酵母人工染色体(YAC)重叠群进行的详细缺失作图确定了两个不同的通常缺失的区域。一个限制在6q21的1-cM区间,旁边是D6S1040和D6S262,另一个限制在6q25.3的1-cM区间,旁边是D6S305和D6S411。在侵袭性实体肾小管癌和硬化性癌中,6q21等位基因丢失的频率高于侵略性组织学类型较弱的肿瘤(P = 0.0006)。 6q25.3等位基因的丢失与孕酮受体的丢失有关(P = 0.0256)。我们的结果表明,在6q上存在两个乳腺癌的抑癌基因,这可能与肿瘤进展和/或激素依赖性丧失有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号