Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 7610001, Israel.
Department of Experimental Medicine I, Nikolaus-Feibiger-Center for Molecular Medicine, University of Erlangen-Nuernberg, 91054 Erlangen, Germany.
Int J Mol Sci. 2021 Dec 31;23(1):445. doi: 10.3390/ijms23010445.
Aberrant activation of Wnt/β-catenin signaling and downstream β-catenin-TCF target genes is a hallmark of colorectal cancer (CRC) development. We identified the immunoglobulin-like cell adhesion receptor L1CAM (L1) as a target of β-catenin-TCF transactivation in CRC cells. Overexpression of L1 in CRC cells confers enhanced proliferation, motility, tumorigenesis, and liver metastasis, and L1 is exclusively localized at invasive areas of human CRC tissue. Several genes are induced after L1 transfection into CRC cells by a mechanism involving the L1-ezrin-NF-κB pathway. We conducted a secretomic analysis of the proteins in the culture medium of L1-overexpressing CRC cells. We detected a highly increased level of biglycan, a small leucine-rich ECM component, and a signaling molecule. We found that induction of biglycan is required for the cellular processes conferred by L1, including enhanced proliferation, motility, tumorigenesis, and liver metastasis. The suppression of endogenous biglycan levels or a point mutation in the L1 ectodomain that regulates cell-cell adhesion mediated by L1 blocked the enhanced tumorigenic properties conferred by L1. The mechanism of biglycan induction by L1 involves the L1-NF-κB pathway. Blocking NF-κB signaling in L1 expressing cells suppressed the induction of biglycan and the tumorigenic properties conferred by L1. Biglycan expression was undetectable in the normal colonic mucosa, but expressed at highly increased levels in the tumor tissue, especially in the stroma. The therapeutic strategies to target biglycan expression might provide a useful approach for CRC treatment in L1-overexpressing tumors.
Wnt/β-catenin 信号通路的异常激活及其下游β-catenin-TCF 靶基因是结直肠癌(CRC)发生的标志。我们发现免疫球蛋白样细胞黏附受体 L1CAM(L1)是 CRC 细胞中β-catenin-TCF 反式激活的靶标。在 CRC 细胞中过表达 L1 可增强增殖、迁移、致瘤性和肝转移,且 L1 仅定位于人 CRC 组织的侵袭区。在 L1 转染 CRC 细胞后,通过 L1-埃兹蛋白-NF-κB 通路参与的机制,有几个基因被诱导。我们对过表达 L1 的 CRC 细胞培养物中的蛋白质进行了分泌组分析。我们检测到富含亮氨酸的细胞外基质(ECM)成分 biglycan 和信号分子的水平显著升高。我们发现,诱导 biglycan 的表达是 L1 赋予细胞的增殖、迁移、致瘤和肝转移等生物学功能所必需的。抑制内源性 biglycan 的水平或 L1 外结构域中的点突变(调节 L1 介导的细胞-细胞黏附)会阻断 L1 赋予的增强的致瘤特性。L1 诱导 biglycan 的机制涉及 L1-NF-κB 通路。在表达 L1 的细胞中阻断 NF-κB 信号通路会抑制 biglycan 的诱导和 L1 赋予的致瘤特性。L1 在正常结肠黏膜中不表达,但在肿瘤组织中高度表达,特别是在基质中。靶向 biglycan 表达的治疗策略可能为 L1 过表达肿瘤的 CRC 治疗提供一种有用的方法。