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伴有完全 situs inversus totalis 的晚期癌症伴 KIF3 复合物缺陷:两例报告。

Advanced cancer with situs inversus totalis associated with KIF3 complex deficiency: report of two cases.

机构信息

Department of Surgery, Tottori Prefectural Central Hospital, 730 Ezu, Tottori, Japan.

出版信息

Surg Today. 2010;40(2):162-6. doi: 10.1007/s00595-009-4005-x. Epub 2010 Jan 28.

Abstract

Situs inversus totalis (SIT) is a relatively rare congenital anomaly, occurring at an incidence of 1 in 10 000-50 000 live births. Although there are some case reports of SIT with the presence of cancer, there are few reports on the relationship between SIT and cancer. However, the recent phylogenetic investigations of this condition suggest that this may be linked to the development and progression of cancer on the molecular level. The key elements are one of the intracellular motor proteins, the KIF3 complex, and the cell-adhesion factors N-cadherin and beta-catenin. We herein present the cases of advanced gastric cancer and lung cancer with SIT, and review the relationship between SIT and the development and progression of cancer.

摘要

全内脏反位(SIT)是一种相对罕见的先天性异常,发生率为每 10000-50000 例活产儿中有 1 例。尽管有一些 SIT 伴发癌症的病例报告,但关于 SIT 与癌症之间关系的报道很少。然而,最近对这种情况的系统发育研究表明,这可能与癌症在分子水平上的发生和发展有关。关键因素之一是细胞内的一种运动蛋白,即 KIF3 复合物,以及细胞黏附因子 N-钙黏蛋白和β-连环蛋白。我们在此介绍了 SIT 合并晚期胃癌和肺癌的病例,并回顾了 SIT 与癌症发生和发展的关系。

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