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骨膜蛋白在癌症进展和转移中的作用:抗骨膜蛋白抗体在小鼠模型中抑制乳腺癌的进展和转移。

Role of periostin in cancer progression and metastasis: inhibition of breast cancer progression and metastasis by anti-periostin antibody in a murine model.

机构信息

Department of Clinical Gene Therapy, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

出版信息

Int J Mol Med. 2011 Aug;28(2):181-6. doi: 10.3892/ijmm.2011.712. Epub 2011 May 26.

Abstract

Periostin (PN), a secreted adhesion-related protein expressed in the periosteum and periodontal ligaments, acts as a critical regulator of the formation and maintenance of bone and teeth, and also plays an important role in tumorigenesis. Although PN is highly expressed in various types of human cancers, its function is still unclear. In this study, we focused on the exon 17 region of PN, which is alternatively spliced out. To investigate the function of full-length PN with exon 17, we produced a neutralizing antibody (PN1-Ab) against the peptide encoded by exon 17. In vivo, administration of PN1-Ab significantly inhibited the growth of primary tumors as well as metastatic tumors, associated with prevention of bone destruction, resulting in increased survival of mice. Consistent with in vivo data, the present in vitro study demonstrated that addition of full-length PN significantly inhibited cell adhesion and detached adherent cells, while PN1-Ab inhibited the action of PN in a dose-dependent manner. In addition, PN1-Ab significantly inhibited the proliferation, migration and invasion of 4T1 mouse breast cancer cells, which produced PN. Interestingly, PN1-Ab also inhibited the differentiation of osteoclasts. Overall, the present study demonstrated that PN plays a pivotal role in the progression and metastasis of breast cancer. Since administration of PN1-Ab prolonged cell survival through inhibition of the progression and metastasis of 4T1 cells, further development of the PN1-Ab such as generation of a humanized antibody may provide a new therapeutic agent against breast cancer.

摘要

骨膜蛋白 (PN) 是一种在骨膜和牙周韧带中表达的分泌型黏附相关蛋白,作为骨和牙齿形成和维持的关键调节剂,在肿瘤发生中也发挥着重要作用。尽管 PN 在各种类型的人类癌症中高度表达,但它的功能仍不清楚。在本研究中,我们专注于 PN 的外显子 17 区域,该区域是选择性剪接的。为了研究具有外显子 17 的全长 PN 的功能,我们针对外显子 17 编码的肽产生了一种中和抗体 (PN1-Ab)。在体内,PN1-Ab 的给药显著抑制了原发性肿瘤和转移性肿瘤的生长,同时预防了骨破坏,从而提高了小鼠的存活率。与体内数据一致,本体外研究表明,添加全长 PN 显著抑制细胞黏附并使黏附细胞脱落,而 PN1-Ab 以剂量依赖性方式抑制 PN 的作用。此外,PN1-Ab 还显著抑制了产生 PN 的 4T1 小鼠乳腺癌细胞的增殖、迁移和侵袭。有趣的是,PN1-Ab 还抑制了破骨细胞的分化。总体而言,本研究表明 PN 在乳腺癌的进展和转移中起关键作用。由于 PN1-Ab 通过抑制 4T1 细胞的进展和转移延长了细胞的存活时间,因此进一步开发 PN1-Ab(例如生成人源化抗体)可能为乳腺癌提供新的治疗剂。

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