Departamento de Gastroenterologia, Laboratorio Metanutri (LIM35), Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Sci Rep. 2019 Apr 3;9(1):5582. doi: 10.1038/s41598-019-42082-4.
We evaluated whether the excluded stomach (ES) after Roux-en-Y gastric bypass (RYGB) can represent a premalignant environment. Twenty obese women were prospectively submitted to double-balloon enteroscopy (DBE) with gastric juice and biopsy collection, before and 3 months after RYGB. We then evaluated morphological and molecular changes by combining endoscopic and histopathological analyses with an integrated untargeted metabolomics and transcriptomics multiplatform. Preoperatively, 16 women already presented with gastric histopathological alterations and an increased pH (≥4.0). These gastric abnormalities worsened after RYGB. A 90-fold increase in the concentration of bile acids was found in ES fluid, which also contained other metabolites commonly found in the intestinal environment, urine, and faeces. In addition, 135 genes were differentially expressed in ES tissue. Combined analysis of metabolic and gene expression data suggested that RYGB promoted activation of biological processes involved in local inflammation, bacteria overgrowth, and cell proliferation sustained by genes involved in carcinogenesis. Accumulated fluid in the ES appears to behave as a potential premalignant environment due to worsening inflammation and changing gene expression patterns that are favorable to the development of cancer. Considering that ES may remain for the rest of the patient's life, long-term ES monitoring is therefore recommended for patients undergoing RYGB.
我们评估了 Roux-en-Y 胃旁路术(RYGB)后被排除的胃(ES)是否可以代表一个癌前环境。二十名肥胖女性前瞻性地接受了双气囊内镜(DBE)检查,包括胃分泌物采集和活检,分别在 RYGB 术前和术后 3 个月进行。然后,我们通过结合内镜和组织病理学分析,以及一个集成的非靶向代谢组学和转录组学多平台,评估了形态和分子变化。术前,16 名女性已经出现了胃组织学改变和 pH 值升高(≥4.0)。这些胃异常在 RYGB 后恶化。ES 液中胆汁酸的浓度增加了 90 倍,ES 液中还含有其他常见于肠道环境、尿液和粪便中的代谢物。此外,ES 组织中有 135 个基因的表达存在差异。代谢和基因表达数据的综合分析表明,RYGB 促进了涉及局部炎症、细菌过度生长和细胞增殖的生物学过程的激活,这些过程受到与癌症发生相关的基因的支持。由于炎症恶化和有利于癌症发展的基因表达模式的改变,积聚在 ES 中的液体似乎表现为一种潜在的癌前环境。鉴于 ES 可能会在患者的余生中存在,因此建议对接受 RYGB 的患者进行长期的 ES 监测。