School of Public Health, Qingdao University.
The Affiliated Qingdao Central Hospital of Qingdao University.
Biol Pharm Bull. 2023 Aug 1;46(8):1145-1151. doi: 10.1248/bpb.b23-00080. Epub 2023 Jun 8.
Inositol hexaphosphate (IP6), a widely found natural bioactive substance in grains, effectively inhibits the progression of colorectal cancer (CRC) when used in combination with inositol (INS). We previously showed that supplementation of IP6 and INS upregulated the claudin 7 gene in orthotropic CRC xenografts in mice. The aim of this study was to elucidate the role of claudin 7 in the inhibition of CRC metastasis by IP6 and INS, and explore the underlying mechanisms. We found that IP6, INS and their combination inhibited the epithelial-mesenchymal transition (EMT) of colon cancer cell lines (SW480 and SW620), as indicated by upregulation of claudin 7 and E-cadherin, and downregulation of N-cadherin. The effect of IP6 and INS was stronger compared to either agent alone (combination index < 1). Furthermore, the silencing of the claudin 7 gene diminished the anti-metastatic effects of IP6 and INS on SW480 and SW620 cells. Consistent with in vitro findings, the combination of IP6 and INS suppressed CRC xenograft growth in a mouse model, which was neutralized by claudin 7. Taken together, the combination of IP6 and INS can inhibit CRC metastasis by blocking EMT of tumor cells through upregulation of claudin 7.
肌醇六磷酸(IP6)是谷物中广泛存在的天然生物活性物质,与肌醇(INS)联合使用时能有效抑制结直肠癌(CRC)的进展。我们之前的研究表明,补充 IP6 和 INS 可上调小鼠原位 CRC 异种移植物中的 claudin 7 基因。本研究旨在阐明 IP6 和 INS 通过上调 claudin 7 抑制 CRC 转移的作用及其潜在机制。我们发现 IP6、INS 及其组合可通过上调 claudin 7 和 E-钙黏蛋白,下调 N-钙黏蛋白,抑制结肠癌细胞系(SW480 和 SW620)的上皮间质转化(EMT)。与单独使用任一药物相比,IP6 和 INS 的效果更强(组合指数<1)。此外,沉默 claudin 7 基因可减弱 IP6 和 INS 对 SW480 和 SW620 细胞的抗转移作用。与体外研究结果一致,IP6 和 INS 的联合使用可抑制 CRC 异种移植物在小鼠模型中的生长,而 claudin 7 可中和其作用。综上所述,IP6 和 INS 的联合使用可通过上调 claudin 7 阻断肿瘤细胞的 EMT 来抑制 CRC 转移。