Division of Molecular Pathology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Department of Cancer Pathology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Biochem Biophys Res Commun. 2021 Jan 1;534:172-178. doi: 10.1016/j.bbrc.2020.11.121. Epub 2020 Dec 6.
Cell adhesion molecule 1 (CADM1), which mediates intercellular adhesion between epithelial cells, is shown to be highly expressed in small-cell lung cancer (SCLC) and to enhance tumorigenicity of SCLC cells in nude mice. Here, we investigated the molecular mechanism underlying the oncogenic role of CADM1 in SCLC. CADM1 promoted colony formation of SCLC cells in soft agar. Analysis of deletion and point mutants of the conserved protein-binding motifs in CADM1 revealed that the 4.1 protein-binding motif in the cytoplasmic domain is responsible for the promotion of colony formation. Among the actin-binding 4.1 proteins, 4.1R was the only protein whose localization to the plasma membrane is dependent on CADM1 expression in SCLC cells. Knockdown of 4.1R suppressed the colony formation enhanced by CADM1, suggesting that 4.1R is required for the oncogenic role of CADM1 in SCLC. In primary SCLC, CADM1 expression was correlated with membranous localization of 4.1R, as was observed in a SCLC cell line. Moreover, membranous co-localization of CADM1 and 4.1R was associated with more advanced tumor stage. These results suggest that the formation of CADM1-4.1R complex would promote malignant features of SCLC.
细胞黏附分子 1(CADM1)介导上皮细胞间的细胞间黏附,在小细胞肺癌(SCLC)中高度表达,并增强 SCLC 细胞在裸鼠中的致瘤性。在这里,我们研究了 CADM1 在 SCLC 中的致癌作用的分子机制。CADM1 促进 SCLC 细胞在软琼脂中的集落形成。对 CADM1 保守蛋白结合基序的缺失和点突变分析表明,细胞质域中的 4.1 蛋白结合基序负责促进集落形成。在肌动蛋白结合的 4.1 蛋白中,4.1R 是唯一一种其在 SCLC 细胞中的定位依赖于 CADM1 表达的蛋白。敲低 4.1R 抑制了 CADM1 增强的集落形成,表明 4.1R 是 CADM1 在 SCLC 中致癌作用所必需的。在原发性 SCLC 中,CADM1 的表达与 4.1R 的膜定位相关,在 SCLC 细胞系中也观察到了这种情况。此外,CADM1 和 4.1R 的膜共定位与更晚期的肿瘤分期相关。这些结果表明,CADM1-4.1R 复合物的形成将促进 SCLC 的恶性特征。