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肝激酶 B1(Lkb1)的肿瘤抑制功能与上皮完整性的调节有关。

Tumor suppressor function of Liver kinase B1 (Lkb1) is linked to regulation of epithelial integrity.

机构信息

Institute of Biomedicine and Genome-Scale Biology Research Program, Biomedicum Helsinki, University of Helsinki, 00014 Helsinki, Finland.

出版信息

Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):E388-97. doi: 10.1073/pnas.1120421109. Epub 2012 Jan 20.

Abstract

Although loss of epithelial integrity is a hallmark of advanced cancer, it remains poorly understood whether genetic alterations corrupting this integrity causally facilitate tumorigenesis. We show that conditional deletion of tumor suppressor gene Lkb1 (Par-4) in the mammary gland compromises epithelial integrity manifested by mislocalization of cell polarity markers, lateralization of tight junctions, deterioration of desmosomes and basement membrane (BM), and hyperbranching of the mammary ductal tree. We identify the desmosomal BM remodelling serine protease Hepsin as a key factor mediating Lkb1 loss-induced structural alterations in mammary epithelium and BM fragmentation. Although loss of Lkb1 alone does not promote mammary tumorigenesis, combination of Lkb1 deficiency with oncogenic c-Myc leads to dramatic acceleration in tumor formation. The results coupling Lkb1 loss-mediated epithelial integrity defects to mislocalization of serine protease Hepsin and to oncogenic synergy with c-Myc imply that Lkb1 loss facilitates oncogenic proliferation by releasing epithelial cells from structural BM boundaries.

摘要

尽管上皮完整性的丧失是癌症晚期的一个标志,但目前仍不清楚破坏这种完整性的遗传改变是否会导致肿瘤发生。我们发现,乳腺中肿瘤抑制基因 Lkb1(Par-4)的条件性缺失会损害上皮完整性,表现为细胞极性标记物的位置异常、紧密连接的侧向化、桥粒和基底膜(BM)的恶化以及乳腺导管树的过度分支。我们确定桥粒 BM 重塑丝氨酸蛋白酶 Hepsin 是介导 Lkb1 缺失诱导的乳腺上皮和 BM 片段化的结构改变的关键因素。尽管单独缺失 Lkb1 本身并不促进乳腺肿瘤发生,但 Lkb1 缺失与致癌基因 c-Myc 的组合会导致肿瘤形成的急剧加速。将 Lkb1 缺失介导的上皮完整性缺陷与丝氨酸蛋白酶 Hepsin 的定位错误以及与 c-Myc 的致癌协同作用相结合的结果表明,Lkb1 缺失通过将上皮细胞从结构 BM 边界释放出来,促进了致癌增殖。

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