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SMAD7维持XIAP表达及大肠癌细胞迁移。

SMAD7 Sustains XIAP Expression and Migration of Colorectal Carcinoma Cells.

作者信息

Colella Marco, Iannucci Andrea, Maresca Claudia, Albano Francesco, Mazzoccoli Carmela, Laudisi Federica, Monteleone Ivan, Monteleone Giovanni

机构信息

Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.

Department of Biomedicine and Prevention, University of Rome "Tor Vergata", 00133 Rome, Italy.

出版信息

Cancers (Basel). 2024 Jun 28;16(13):2370. doi: 10.3390/cancers16132370.

Abstract

The reorganization of the cell cytoskeleton and changes in the content of cell adhesion molecules are crucial during the metastatic spread of tumor cells. Colorectal cancer (CRC) cells express high SMAD7, a protein involved in the control of CRC cell growth. In the present study, we evaluated whether SMAD7 regulates the cytoskeleton reorganization and dynamics in CRC. Knockdown of SMAD7 with a specific antisense oligonucleotide (AS) in HCT116 and DLD1, two human CRC cell lines, reduced the migration rate and the content of F-ACTIN filaments. A gene array, real-time PCR, and Western blotting of SMAD7 AS-treated cells showed a marked down-regulation of the X-linked inhibitor of apoptosis protein (XIAP), a member of the inhibitor of apoptosis family, which has been implicated in cancer cell migration. IL-6 and IL-22, two cytokines that activate STAT3, enhanced XIAP in cancer cells, and such induction was attenuated in SMAD7-deficient cells. Finally, in human CRC, mRNA correlated with expression. Our data show that positively regulates expression and migration of CRC cells, and suggest a mechanism by which SMAD7 controls the architecture components of the CRC cell cytoskeleton.

摘要

在肿瘤细胞的转移扩散过程中,细胞细胞骨架的重组和细胞黏附分子含量的变化至关重要。结肠直肠癌(CRC)细胞高表达SMAD7,一种参与控制CRC细胞生长的蛋白质。在本研究中,我们评估了SMAD7是否调节CRC中的细胞骨架重组和动态变化。在两种人CRC细胞系HCT116和DLD1中用特异性反义寡核苷酸(AS)敲低SMAD7,降低了迁移率和F-肌动蛋白丝的含量。对经SMAD7 AS处理的细胞进行基因芯片、实时PCR和蛋白质印迹分析,结果显示凋亡抑制蛋白家族成员X连锁凋亡抑制蛋白(XIAP)明显下调,XIAP与癌细胞迁移有关。激活STAT3的两种细胞因子IL-6和IL-22增强了癌细胞中的XIAP,而在SMAD7缺陷细胞中这种诱导作用减弱。最后,在人CRC中,mRNA与表达相关。我们的数据表明, 正向调节CRC细胞的表达和迁移,并提示了一种SMAD7控制CRC细胞细胞骨架结构成分的机制。 (注:原文中部分内容缺失,翻译时保留了原文格式)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb1/11240366/f49da758ef57/cancers-16-02370-g001.jpg

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