补体调节蛋白CD46在促进膀胱癌症细胞迁移中发挥独特作用。

Chonnam medical journal Pub Date : 2023-09-01 Epub Date: 2023-09-25 DOI:10.4068/cmj.2023.59.3.160
Thuy Thi Nguyen, Hien Duong Thanh, Manh-Hung Do, Chaeyong Jung
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引用次数: 0

摘要

CD46是一种膜结合补体调节蛋白(mCRP),对补体系统具有调节作用。CD46保护宿主细胞免受补体的损伤。CD46的表达在包括膀胱癌在内的许多癌症中也高度维持,因此作为许多癌症治疗性病毒的受体发挥作用。在这项研究中,我们报道了CD46作为癌症细胞在膀胱癌中的一种进展因子的独特作用。来自使用CD46改变的HT1376膀胱癌的DNA微阵列的结果数据证明了靶基因库,包括补体C3α链(C3α)、基质Gla蛋白(MGP)、AFAP-AS1、滤泡树突状细胞分泌蛋白(FDCSP)、含MAM结构域2(MAMDC2)、γ-氨基丁酸a受体pi(GABRP)、转化生长因子,细胞色素P450(CYP24A1)、唾液酸结合Ig样凝集素6(SIGLEC6)、金属硫蛋白1E(MT1E)和细胞角蛋白的几个成员的家族。随后使用定量RT-PCR和蛋白质印迹分析的研究证实了CD46介导的C3α、MGP和角蛋白13(KRT13)的调节。MGP和KRT13已知参与细胞迁移和癌症细胞转移。细胞迁移测定表明,CD46增强了膀胱癌症细胞的迁移潜力。总之,该报告表明,CD46在膀胱癌中通常过表达,并在促进癌症细胞迁移中发挥独特作用。需要进一步的详细研究来阐明CD46的作用机制及其在癌症治疗中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Complement Regulatory Protein CD46 Manifests a Unique Role in Promoting the Migration of Bladder Cancer Cells.

Complement Regulatory Protein CD46 Manifests a Unique Role in Promoting the Migration of Bladder Cancer Cells.

Complement Regulatory Protein CD46 Manifests a Unique Role in Promoting the Migration of Bladder Cancer Cells.

Complement Regulatory Protein CD46 Manifests a Unique Role in Promoting the Migration of Bladder Cancer Cells.

CD46 is a membrane-bound complement regulatory protein (mCRP) possessing a regulatory role with the complement system. CD46 protects the host cells from damage by complement. Expression of CD46 is also highly maintained in many cancers, including bladder cancers, and thus functions as a receptor for many cancer therapeutic viruses. In this study we report a unique role of CD46 as a progression factor of cancer cells in bladder cancers. Resulting data from a DNA microarray using CD46-altered HT1376 bladder cancers demonstrated a pool of target genes, including complement C3 α chain (C3α), matrix Gla protein (MGP), AFAP-AS1, follicular dendritic cell secreted protein (FDCSP), MAM domain containing 2 (MAMDC2), gamma-aminobutyric acid A receptor pi (GABRP), transforming growth factor, beta-induced (TGFBI), a family of cytochrome P450 (CYP24A1), sialic acid binding Ig-like lectin 6 (SIGLEC6), metallothionein 1E (MT1E), and several members of cytokeratins. Subsequent studies using quantitative RT-PCR and Western blot analyses confirmed CD46-mediated regulation of C3α, MGP, and keratin 13 (KRT13). MGP and KRT13 are known to be involved in cell migration and cancer cell metastasis. A cell migration assay demonstrated that CD46 enhanced migratory potential of bladder cancer cells. Taken all together, this report demonstrated that CD46 is generally overexpressed in bladder cancers and plays a unique role in the promotion of cancer cell migration. Further detailed studies are needed to be performed to clarify the action mechanism of CD46 and its application to cancer therapeutics.

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