Suppr超能文献

结直肠癌肝转移中的染色体等位基因缺失及其与临床特征的关联。

Chromosome allele loss in colorectal liver metastases and its association with clinical features.

作者信息

Ding S F, Delhanty J D, Zografos G, Michail N E, Dooley J S, Habib N A

机构信息

Department of Surgery, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.

出版信息

Br J Surg. 1994 Jun;81(6):875-8. doi: 10.1002/bjs.1800810627.

Abstract

Molecular genetic changes are better characterized in colorectal carcinoma than in other common adult tumours. Consistent allele losses, or loss of heterozygosity (LOH), on chromosomes 5q, 17p and 18q have been well established. These changes are associated with the prognosis of the disease. Little is known of such changes in liver metastases of colorectal origin. The extent of allelic loss and its association with clinical features were investigated in 19 patients with colorectal liver metastases by using 24 probes to detect restriction fragment length polymorphism. A high frequency of LOH on chromosomes 5q, 17p and 18q was found in these secondary tumours. No consistent loss has so far been shown in any other chromosome. The frequency of allele loss correlated significantly with prognostic features such as the number and size of liver secondaries (P < 0.005), metastasis to the lymph nodes (P < 0.01) and curative or palliative operation (P < 0.02).

摘要

与其他常见的成人肿瘤相比,结直肠癌的分子遗传学变化得到了更好的描述。5号染色体长臂、17号染色体短臂和18号染色体长臂上一致的等位基因缺失或杂合性缺失(LOH)已得到充分证实。这些变化与疾病的预后相关。对于结直肠来源的肝转移瘤中的此类变化,人们了解甚少。通过使用24个探针检测限制性片段长度多态性,对19例结直肠肝转移患者的等位基因缺失程度及其与临床特征的关联进行了研究。在这些继发性肿瘤中发现5号染色体长臂、17号染色体短臂和18号染色体长臂上存在高频率的杂合性缺失。目前尚未在任何其他染色体上显示出一致的缺失。等位基因缺失的频率与预后特征显著相关,如肝转移瘤的数量和大小(P < 0.005)、淋巴结转移(P < 0.01)以及根治性或姑息性手术(P < 0.02)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验