四跨膜蛋白CD81介导人骨肉瘤的生长和转移

IF 4.8 2区 医学 Q1 Medicine Cellular Oncology Pub Date : 2019-12-01 Epub Date: 2019-09-07 DOI:10.1007/s13402-019-00472-w
Naoki Mizoshiri, Toshiharu Shirai, Ryu Terauchi, Shinji Tsuchida, Yuki Mori, Daichi Hayashi, Tsunao Kishida, Yuji Arai, Osam Mazda, Tohru Nakanishi, Toshikazu Kubo
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引用次数: 0

摘要

目的:CD81是膜蛋白四跨蛋白家族的一员。近年来,有研究表明CD81可能参与了癌细胞的增殖和转移。然而,目前关于CD81在骨肉瘤中的表达和作用的报道很少。方法:研究CD81在人成骨细胞系hFOB1.19和人骨肉瘤细胞系Saos2、MG63、143B中的表达。使用siRNA抑制骨肉瘤细胞中CD81的表达,然后评估细胞增殖、迁移和侵袭。Western blotting检测Akt、Erk、JNK和p38的磷酸化状态,并检测MMP-2、MMP-9和MT1-MMP的表达。此外,我们使用CRISPR/Cas9系统稳定敲除143B细胞中的CD81表达,将细胞移植到小鼠体内,并与对照组比较,评估这些小鼠的肿瘤形成和肺转移情况。结果:我们发现CD81在人成骨细胞系和所有骨肉瘤细胞系中均有表达。骨肉瘤细胞系143B表现出特别高的表达水平。此外,我们发现CD81抑制后,骨肉瘤细胞的增殖、迁移和侵袭减少,Akt和Erk的磷酸化受到抑制。MMP-2、MMP-9和MT1-MMP的表达均受到抑制,其中MMP-9的表达受抑制程度最大。在体内,我们发现移植CD81敲除143B细胞的小鼠肿瘤形成和肺转移明显少于对照组小鼠。结论:基于我们的研究结果,我们得出抑制CD81可以抑制骨肉瘤细胞内的信号传导,减少骨肉瘤细胞的肿瘤发生和肺转移。
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The tetraspanin CD81 mediates the growth and metastases of human osteosarcoma.

Purpose: CD81 is a member of the tetraspanin family of membrane proteins. Recently, it has been shown that CD81 may be involved in cancer cell proliferation and metastasis. As yet, however, there have been few reports on the expression and role of CD81 in osteosarcoma.

Methods: The expression of CD81 was investigated in human osteoblast cell line hFOB1.19 and in human osteosarcoma cell lines Saos2, MG63 and 143B. The expression of CD81 was inhibited in osteosarcoma cells using siRNA after which cell proliferation, migration and invasion were assessed. We also used Western blotting to investigate the phosphorylation status of Akt, Erk, JNK and p38, and measured the expression of MMP-2, MMP-9 and MT1-MMP. In addition, we used a CRISPR/Cas9 system to stably knock out CD81 expression in 143B cells, transplanted the cells into mice, and assessed tumor formation and lung metastasis in these mice compared to those in the control group.

Results: We found that CD81 was expressed in the human osteoblast cell line and in all osteosarcoma cell lines tested. The osteosarcoma cell line 143B exhibited a particularly high level of expression. In addition, we found that osteosarcoma cell proliferation, migration and invasion were decreased after CD81 inhibition, and that the phosphorylation of Akt and Erk was suppressed. Also, the expression levels of MMP-2, MMP-9 and MT1-MMP were found to be suppressed, with MMP-9 showing the greatest suppression. In vivo, we found that mice transplanted with CD81 knockout 143B cells exhibited significantly less tumor formation and lung metastasis than mice in the control group.

Conclusion: Based on our findings we conclude that inhibition of CD81 suppresses intracellular signaling and reduces tumorigenesis and lung metastasis in osteosarcoma cells.

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来源期刊
Cellular Oncology
Cellular Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
10.40
自引率
1.50%
发文量
0
审稿时长
16 weeks
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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