生物
癌症研究
体内
前列腺癌
间质细胞
前列腺
癌症
基因敲除
跨膜蛋白
细胞内
细胞生物学
细胞培养
受体
遗传学
生物化学
生物技术
作者
Takashi Yamamoto,Yasuaki Tamura,Jun’ichi Kobayashi,Kenjirou Kamiguchi,Yoshihiko Hirohashi,Akira Miyazaki,Toshihiko Torigoe,Hiroko Asanuma,Hiroyoshi Hiratsuka,Noriyuki Sato
标识
DOI:10.1016/j.yexcr.2013.07.025
摘要
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.
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