Saito Motonobu, Okayama Hirokazu, Saito Katsuharu, Ando Jin, Kumamoto Kensuke, Nakamura Izumi, Ohki Shinji, Ishi Yoshimasa, Takenoshita Seiichi
Department of Organ Regulatory Surgery, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan.
Division of Genome Biology, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
Oncol Lett. 2017 Nov;14(5):6184-6190. doi: 10.3892/ol.2017.6956. Epub 2017 Sep 15.
The development of gastric cancer is significantly associated with chronic inflammation, such as caused by infection. Caudal-type homeobox 2 (CDX2) is a homeobox protein involved in intestinal differentiation in normal and in aberrant locations, and is associated with inflammation. The authors of the present study have previously reported that CDX2 may have a suppressive role in the progression and carcinogenesis of gastric carcinoma. In the present study, the authors initially confirmed that a decreased expression of CDX2, as detected by immunohistochemistry, is associated with poor cancer-specific survival in 210 gastric cancer cases, which is consistent with several previously published studies. To elucidate the potential mechanisms underlying this association, the authors investigated the mechanism of CDX2 suppression, which included interleukin (IL)-6/signal transducer and activator of transcription 3 (STAT3) and p53 signaling pathways. The present study confirmed that CDX2 was suppressed by activation of the IL-6/STAT3 signaling pathway via miR-181b . It was further revealed that gastric cancer with negative CDX2 expression is associated with negative p53 staining, and this association was particularly significant in undifferentiated gastric cancer. The activation of the IL-6/STAT3 signaling pathway suppressed miR-34a, which is induced by p53. This suggests that the activation of the IL-6/STAT3 signaling pathway inflammation signaling pathway suppresses the p53 signaling pathway in tumors without mutation, which results in poor prognostic outcomes. In conclusion, CDX2 may be a useful prognostic biomarker for gastric cancer and is associated with p53 inactivation.
胃癌的发生与慢性炎症密切相关,如感染所致的炎症。尾型同源盒2(CDX2)是一种参与正常及异常部位肠道分化的同源盒蛋白,且与炎症相关。本研究的作者此前曾报道,CDX2可能在胃癌的进展和致癌过程中发挥抑制作用。在本研究中,作者首先通过免疫组织化学检测证实,CDX2表达降低与210例胃癌患者较差的癌症特异性生存率相关,这与之前发表的几项研究一致。为了阐明这种关联背后的潜在机制,作者研究了CDX2抑制的机制,其中包括白细胞介素(IL)-6/信号转导和转录激活因子3(STAT3)以及p53信号通路。本研究证实,IL-6/STAT3信号通路通过miR-181b激活而抑制CDX2。进一步发现,CDX2表达阴性的胃癌与p53染色阴性相关,且这种关联在未分化胃癌中尤为显著。IL-6/STAT3信号通路的激活抑制了由p53诱导的miR-34a。这表明,IL-6/STAT3信号通路的激活在无突变的肿瘤中抑制了p53信号通路,从而导致预后不良。总之,CDX2可能是一种有用的胃癌预后生物标志物,且与p53失活相关。