Uchida Daisuke, Shiraha Hidenori, Kato Hironari, Sawahara Hiroaki, Nagahara Teruya, Iwamuro Masaya, Kataoka Junro, Horiguchi Shigeru, Watanabe Masami, Takaki Akinobu, Nouso Kazuhiro, Nasu Yasutomo, Kumon Hiromi, Yamamoto Kazuhide
Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
J Gastroenterol Hepatol. 2016 Jun;31(6):1154-9. doi: 10.1111/jgh.13259.
Reduced expression in immortalized cells/dickkopf-3 (REIC/DKK3) is a reported tumor suppressor gene and has potential to become an innovative therapy for various cancers. We examined the antitumor immunological effects of human REIC/DKK3 protein against pancreatic cancer.
Activation of extracellular signal-regulated kinases 1 and 2, mammalian target of rapamycin, and signal transducer and activator of transcription 3 by REIC/DKK3 protein was assessed in human peripheral blood mononuclear cells using immunoblotting. Pancreatic cancer cell lines (AsPC-1 and MIA Paca-2) were cocultured with peripheral blood mononuclear cells, and the anticancer effects of REIC/DKK3 protein were assessed using the methyl thiazole tetrazolium, cytotoxicity, and enzyme-linked immunospot assays. The antitumor immunological effects of the combined treatment with REIC/DKK3 protein and peripheral blood mononuclear cells were also assessed in a pancreatic cancer model using non-obese diabetic/severe combined immunodeficiency mice.
The REIC/DKK3 protein activated extracellular signal-regulated kinases 1 and 2, mammalian target of rapamycin, and signal transducer and activator of transcription 3 in peripheral blood mononuclear cells. REIC/DKK3 protein inhibited in vitro cancer cell viability and enhanced cytotoxicity when incubated with peripheral blood mononuclear cells. REIC/DKK3 protein induced significant production of interferon gamma from lymphocytes incubated with pancreatic cancer cells, indicating that CD8+ T cells were activated in the peripheral blood mononuclear cells when cocultured with AsPC-1 and MIA Paca-2 in the presence of REIC/DKK3 protein. Combined treatment with REIC/DKK3 protein and peripheral blood mononuclear cells produced in vivo anticancer immunostimulatory effects on pancreatic cancer cells.
The REIC/DKK3 protein and peripheral blood mononuclear cells synergistically enhanced anticancer immunological effects against pancreatic cancer cells. The observed immunomodulatory effect of combined treatment likely occurs in adenovirus-mediated REIC/DKK3 gene therapy and provides important clues to the therapeutic mechanisms involving immune cells.
永生细胞/ Dickkopf - 3(REIC/DKK3)表达降低是一种已报道的肿瘤抑制基因,有潜力成为各种癌症的创新治疗方法。我们研究了人REIC/DKK3蛋白对胰腺癌的抗肿瘤免疫效应。
使用免疫印迹法在人外周血单个核细胞中评估REIC/DKK3蛋白对细胞外信号调节激酶1和2、雷帕霉素靶蛋白以及信号转导和转录激活因子3的激活作用。将胰腺癌细胞系(AsPC - 1和MIA Paca - 2)与外周血单个核细胞共培养,使用甲基噻唑四氮唑、细胞毒性和酶联免疫斑点试验评估REIC/DKK3蛋白的抗癌作用。还在非肥胖糖尿病/严重联合免疫缺陷小鼠的胰腺癌模型中评估了REIC/DKK3蛋白与外周血单个核细胞联合治疗的抗肿瘤免疫效应。
REIC/DKK3蛋白激活了外周血单个核细胞中的细胞外信号调节激酶1和2、雷帕霉素靶蛋白以及信号转导和转录激活因子3。REIC/DKK3蛋白与外周血单个核细胞一起孵育时,抑制了体外癌细胞活力并增强了细胞毒性。REIC/DKK3蛋白诱导与胰腺癌细胞孵育的淋巴细胞产生大量γ干扰素,表明在REIC/DKK3蛋白存在的情况下,与AsPC - 1和MIA Paca - 2共培养时,外周血单个核细胞中的CD8 + T细胞被激活。REIC/DKK3蛋白与外周血单个核细胞联合治疗对胰腺癌细胞产生了体内抗癌免疫刺激作用。
REIC/DKK3蛋白与外周血单个核细胞协同增强了对胰腺癌细胞的抗癌免疫效应。联合治疗观察到的免疫调节作用可能发生在腺病毒介导的REIC/DKK3基因治疗中,并为涉及免疫细胞的治疗机制提供了重要线索。