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质子泵抑制剂奥美拉唑抑制 F344 大鼠致癌物诱导的结肠腺瘤向腺癌的进展。

Proton Pump Inhibitor Omeprazole Suppresses Carcinogen-induced Colonic Adenoma Progression to Adenocarcinoma in F344 Rat.

机构信息

Center for Cancer Prevention and Drug Development, Hematology-Oncology Section, Department of Medicine, Stephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.

Division of Cancer Prevention, Chemopreventive Agent Development Research Group, NCI, Rockville, Maryland.

出版信息

Cancer Prev Res (Phila). 2021 Nov;14(11):1009-1020. doi: 10.1158/1940-6207.CAPR-21-0057. Epub 2021 Aug 2.

Abstract

Colorectal cancer causes over 53,000 deaths annually in the United States. Its rising incidences worldwide and particularly in young adults is a major concern. Here, we evaluated the efficacy of omeprazole that is clinically approved for treating acid reflux, to enable its repurposing for colorectal cancer prevention. In the azoxymethane-induced rat colorectal cancer model, dietary omeprazole (250 and 500 ppm) was administered at early adenoma stage (8 weeks after azoxymethane) to assess the progression of early lesions to adenocarcinoma. Administration of omeprazole at 250 or 500 ppm doses led to suppression of total colon adenocarcinoma incidence by 15.7% and 32% ( < 0.01), respectively. Importantly, invasive carcinoma incidence was reduced by 59% ( < 0.0005) and 90% ( < 0.0001) in omeprazole-administered rats in a dose-dependent manner. There was also a strong and dose-dependent inhibition in the adenocarcinoma multiplicity in rats exposed to omeprazole. Administration of 250 and 500 ppm omeprazole inhibited total colon adenocarcinoma multiplicity by approximately 49% and approximately 65% ( < 0.0001), respectively. While noninvasive adenocarcinomas multiplicity was suppressed by approximately 34% to approximately 48% ( < 0.02), the invasive carcinomas multiplicity was reduced by approximately 74% to approximately 94% ( < 0.0001) in omeprazole-exposed rats in comparison with the untreated rats. Biomarker analysis results showed a decrease in cell proliferation and anti-apoptotic/pro-survival proteins with an increase in apoptosis. Transcriptome analysis of treated tumors revealed a significant increase in adenocarcinoma inhibitory genes (Olmf4; Spink4) expression and downregulation of progression promoting genes (SerpinA1, MMP21, IL6). In summary, omeprazole showed significant protection against the progression of adenoma to adenocarcinoma. PREVENTION RELEVANCE: Preventing colon cancer is urgently needed because of its high incidence and mortality rates worldwide. Toward this end, preventive efficacy of omeprazole, a common medication, was evaluated in animal model of colorectal cancer and was found to suppress colonic adenoma progression to carcinoma. These findings warrant its further evaluation in humans.

摘要

结直肠癌每年导致美国超过 53000 人死亡。其在全球范围内,尤其是在年轻人中的发病率不断上升,令人担忧。在这里,我们评估了临床上用于治疗胃酸反流的奥美拉唑的疗效,以使其能够重新用于预防结直肠癌。在氧化偶氮甲烷诱导的大鼠结直肠癌模型中,在早腺瘤阶段(氧化偶氮甲烷后 8 周)给予饮食奥美拉唑(250 和 500ppm),以评估早期病变向腺癌的进展。奥美拉唑 250 或 500ppm 剂量给药可使全结肠腺癌发生率分别降低 15.7%和 32%(<0.01)。重要的是,奥美拉唑给药大鼠的侵袭性癌发生率分别降低 59%(<0.0005)和 90%(<0.0001),呈剂量依赖性。在暴露于奥美拉唑的大鼠中,腺癌的多发性也有强烈的、剂量依赖性抑制。奥美拉唑给药可使大鼠全结肠腺癌多发性分别降低约 49%和 65%(<0.0001)。非侵袭性腺癌多发性降低约 34%至 48%(<0.02),而侵袭性癌多发性降低约 74%至 94%(<0.0001)。生物标志物分析结果表明,细胞增殖和抗凋亡/存活蛋白减少,凋亡增加。治疗肿瘤的转录组分析显示,腺癌抑制基因(Olmf4;Spink4)表达增加,促进进展的基因(SerpinA1、MMP21、IL6)下调。总之,奥美拉唑对腺瘤向腺癌的进展有显著的保护作用。预防意义:由于结直肠癌在全球的发病率和死亡率都很高,因此迫切需要预防。为此,我们评估了一种常见药物奥美拉唑在结直肠癌动物模型中的预防效果,发现它能抑制结肠腺瘤向癌的进展。这些发现值得进一步在人类中进行评估。

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