Konishi Hidetomo, Asano Naoki, Imatani Akira, Kimura Osamu, Kondo Yutaka, Jin Xiaoyi, Kanno Takeshi, Hatta Waku, Ara Nobuyuki, Asanuma Kiyotaka, Koike Tomoyuki, Shimosegawa Tooru
Division of Gastroenterology, Tohoku University Graduate School of Medicine, Aoba-ku, Sendai, Miyagi 980-8574, Japan.
Oncotarget. 2016 Aug 30;7(35):56598-56607. doi: 10.18632/oncotarget.10967.
CD133 is considered as a stem-like cell marker in some cancers including gastric cancers, and Notch1 signaling is known to play an important role in the maintenance and differentiation of stem-like cells. We aimed to investigate whether Notch1 signaling contributes to the carcinogenesis of gastric cancers and CD133 induction. CD133 expression was detected in 51.4% of diffuse type gastric cancers while it was not detected in intestinal type gastric cancers. Similarly, only poorly-differentiated gastric cancer cell lines expressed CD133 and activated-Notch1. Inhibiting Notch1 signaling resulted in decreased CD133 expression, side population cells, cell proliferation and anchorage independent cell growth. Chromatin immunoprecipitation suggested that this Notch1 dependent regulation of CD133 was caused by direct binding of activated-Notch1 to the RBP-Jκ binding site in the 5' promoter region of CD133 gene. In addition, knocking down RBP-Jκ reduced CD133 induction in activated-Notch1 transfected cells. These findings suggested that Notch1 signaling plays an important role in the maintenance of the cancer stem-like phenotype in diffuse type gastric cancer through an RBP-Jκ dependent pathway and that inhibiting Notch1 signaling could be an effective therapy against CD133 positive diffuse type gastric cancers.
CD133在包括胃癌在内的某些癌症中被视为一种干细胞样标志物,并且已知Notch1信号传导在干细胞样细胞的维持和分化中起重要作用。我们旨在研究Notch1信号传导是否有助于胃癌的致癌作用和CD133的诱导。在51.4%的弥漫型胃癌中检测到CD133表达,而在肠型胃癌中未检测到。同样,只有低分化胃癌细胞系表达CD133和活化的Notch1。抑制Notch1信号传导导致CD133表达、侧群细胞、细胞增殖和锚定非依赖性细胞生长减少。染色质免疫沉淀表明,CD133的这种Notch1依赖性调节是由活化的Notch1与CD133基因5'启动子区域中的RBP-Jκ结合位点直接结合引起的。此外,敲低RBP-Jκ可降低活化的Notch1转染细胞中的CD133诱导。这些发现表明,Notch1信号传导通过RBP-Jκ依赖性途径在弥漫型胃癌的癌干细胞样表型维持中起重要作用,并且抑制Notch1信号传导可能是针对CD133阳性弥漫型胃癌的有效治疗方法。