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

被引:90
|
作者
Kyutoku, Mariko [1 ]
Taniyama, Yoshiaki [1 ,2 ]
Katsuragi, Naruto [3 ]
Shimizu, Hideo [1 ,2 ]
Kunugza, Yasuo [1 ]
Iekushi, Kazuma [1 ,2 ]
Koibuchi, Nobutaka [4 ]
Sanada, Fumthiro [1 ]
Oshita, Yoshihiro [1 ]
Morishita, Ryuichi [1 ]
机构
[1] Osaka Univ, Dept Clin Gene Therapy, Grad Sch Med, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Dept Geriatr Med & Nephrol, Grad Sch Med, Suita, Osaka 5650871, Japan
[3] Asubio Pharma Co Ltd, Biomed Res Labs, Chuo Ku, Kobe, Hyogo 6500047, Japan
[4] Kumamoto Univ, Grad Sch Med Sci, Dept Pharmacol & Mol Therapeut, Kumamoto 8608556, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
breast cancer; periostin; anti-periostin antibody; ACUTE MYOCARDIAL-INFARCTION; GROWTH; EXPRESSION; BONE; ANGIOGENESIS; INVASION; PROTEIN;
D O I
10.3892/ijmm.2011.712
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:181 / 186
页数:6
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