Araki Kentaro, Wakabayashi Hiroki, Shintani Ken, Morikawa Joji, Matsumine Akihiko, Kusuzaki Katsuyuki, Sudo Akihiro, Uchida Atsumasa
Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Mie, Japan.
Oncology. 2009;77(2):92-9. doi: 10.1159/000228253. Epub 2009 Jul 7.
Decorin, the prototype of an expanding family of small leucine-rich proteoglycans, is involved in a number of cellular processes including matrix assembly, fibrillogenesis and the control of cell proliferation. In this study, we investigated the role of decorin in suppressing tumor aggressiveness and bone metastases. We used a metastatic breast cancer cell line, MDA-MB-231, to show that decorin causes marked growth suppression bothin vitro and in vivo. A cytomegaloviral vector containing the decorin transgene caused greatly reduced cell growth, motility and observed metastases. Bone metastases were decreased by >90% upon decorin transfection. These results demonstrate a novel role for decorin in the reduction or prevention of tumor metastases in this breast cancer model and could eventually lead to improved therapies for metastatic breast cancer.
核心蛋白聚糖是富含亮氨酸的小分子蛋白聚糖不断扩展的家族中的原型,参与包括基质组装、纤维形成和细胞增殖控制在内的许多细胞过程。在本研究中,我们调查了核心蛋白聚糖在抑制肿瘤侵袭性和骨转移中的作用。我们使用转移性乳腺癌细胞系MDA-MB-231来表明核心蛋白聚糖在体外和体内均能引起显著的生长抑制。含有核心蛋白聚糖转基因的巨细胞病毒载体导致细胞生长、运动性和观察到的转移显著减少。转染核心蛋白聚糖后,骨转移减少了90%以上。这些结果证明了核心蛋白聚糖在该乳腺癌模型中减少或预防肿瘤转移方面的新作用,并最终可能导致转移性乳腺癌治疗方法的改进。