Department of Pathology, Sapporo Medical University School of Medicine, South 1, West 17, Chuo-ku, Sapporo 060-8556, Japan; Department of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Exp Cell Res. 2013 Oct 15;319(17):2617-26. doi: 10.1016/j.yexcr.2013.07.025. Epub 2013 Aug 2.
Six-transmembrane epithelial antigen of the prostate-1 (STEAP-1) is a novel cell surface protein overexpressed only in the prostate among normal tissues and various types of cancer including prostate, bladder, lung, and ovarian cancer. Although its function in prostate and tumor cells has been remained unclear, due to its unique and restricted expression, STEAP-1 is expected to be an attractive target for cancer therapy. Here, we show that knockdown of STEAP-1 in human cancer cells caused the retardation of tumor growth compared with wild type in vivo. In contrast, STEAP-1 introduced tumor cells augmented the tumor growth compared with STEAP-1-negative wild type cells. Using dye transfer assay, we demonstrate that the STEAP-1 is involved in intercellular communication between tumor cells and adjacent tumor stromal cells and therefore may play a key role for the tumor growth in vivo. These data indicate the inhibition of the STEAP-1 function or expression can be a new strategy for cancer therapy.
六跨膜上皮抗原前列腺-1(STEAP-1)是一种新型的细胞表面蛋白,仅在前列腺组织和各种类型的癌症中过度表达,包括前列腺癌、膀胱癌、肺癌和卵巢癌。尽管其在前列腺和肿瘤细胞中的功能尚不清楚,但由于其独特和受限的表达,STEAP-1有望成为癌症治疗的一个有吸引力的靶点。在这里,我们显示,在体内,与野生型相比,STEAP-1 敲低的人癌细胞的肿瘤生长速度减慢。相比之下,STEAP-1 导入的肿瘤细胞与 STEAP-1 阴性的野生型细胞相比,增强了肿瘤的生长。通过染料转移实验,我们证明 STEAP-1 参与肿瘤细胞与相邻肿瘤基质细胞之间的细胞间通讯,因此可能在体内肿瘤生长中起关键作用。这些数据表明抑制 STEAP-1 的功能或表达可能是癌症治疗的一种新策略。