Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Prev Res (Phila). 2021 Sep;14(9):851-862. doi: 10.1158/1940-6207.CAPR-20-0496. Epub 2021 Jul 15.
Familial adenomatous polyposis (FAP) is a hereditary colorectal cancer syndrome, which results in the development of hundreds of adenomatous polyps carpeting the gastrointestinal tract. NSAIDs have reduced polyp burden in patients with FAP and synthetic rexinoids have demonstrated the ability to modulate cytokine-mediated inflammation and WNT signaling. This study examined the use of the combination of an NSAID (sulindac) and a rexinoid (bexarotene) as a durable approach for reducing FAP colonic polyposis to prevent colorectal cancer development. Whole transcriptomic analysis of colorectal polyps and matched normal mucosa in a cohort of patients with FAP to identify potential targets for prevention in FAP was performed. Drug-dose synergism of sulindac and bexarotene in cell lines and patient-derived organoids was assessed, and the drug combination was tested in two different mouse models. This work explored mRNA as a potential predictive serum biomarker for this combination in FAP. Overall, transcriptomic analysis revealed significant activation of inflammatory and cell proliferation pathways. A synergistic effect of sulindac (300 μmol/L) and bexarotene (40 μmol/L) was observed in FAP colonic organoids with primary targeting of polyp tissue compared with normal mucosa. This combination translated into a significant reduction in polyp development in and mice. Finally, the reported data suggest miRNA-21 could serve as a predictive serum biomarker for polyposis burden in patients with FAP. These findings support the clinical development of the combination of sulindac and bexarotene as a treatment modality for patients with FAP. PREVENTION RELEVANCE: This study identified a novel chemopreventive regimen combining sulindac and bexarotene to reduce polyposis in patients with FAP using tools, , and models. This investigation provides the essential groundwork for moving this drug combination forward into a clinical trial.
家族性腺瘤性息肉病(FAP)是一种遗传性结直肠癌综合征,导致胃肠道内出现数百个腺瘤性息肉。非甾体抗炎药(NSAIDs)可减轻 FAP 患者的息肉负担,合成维甲酸已证明具有调节细胞因子介导的炎症和 WNT 信号的能力。本研究探讨了 NSAID(舒林酸)和维甲酸(贝沙罗汀)联合作为减少 FAP 结肠息肉以预防结直肠癌发展的持久方法的应用。对 FAP 患者队列的结直肠息肉和匹配的正常黏膜进行全转录组分析,以确定 FAP 中预防的潜在靶点。评估了舒林酸和贝沙罗汀在细胞系和患者来源的类器官中的药物剂量协同作用,并在两种不同的小鼠模型中测试了药物组合。这项工作探索了 mRNA 作为 FAP 中这种组合的潜在预测性血清生物标志物。总体而言,转录组分析显示炎症和细胞增殖途径的显著激活。与正常黏膜相比,舒林酸(300μmol/L)和贝沙罗汀(40μmol/L)在 FAP 结肠类器官中观察到协同作用,主要针对息肉组织。这种组合在 和 小鼠中导致息肉发育显著减少。最后,报告的数据表明 miRNA-21 可作为 FAP 患者息肉负担的预测性血清生物标志物。这些发现支持将舒林酸和贝沙罗汀联合作为 FAP 患者治疗方法的临床开发。预防相关性:本研究使用 、 和 模型,确定了一种新的联合舒林酸和贝沙罗汀的化学预防方案,以减少 FAP 患者的息肉形成。这项研究为将这种药物组合推进临床试验提供了必要的基础。