LB220:人类结肠上皮细胞分化和生长控制:比较临床试验结果和人类结肠样细胞培养反应

M. Aslam, S. Mcclintock, M. A. H. Jawad-Makki, K. Knuver, Daniyal M. Nadeem, H. Ahmad, D. Attili, D. Turgeon, J. Varani
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引用次数: 0

摘要

作为我们努力了解微量元素在结肠息肉化学预防中的作用的一部分,我们进行了结肠体培养(离体)和人体受试者(体内)研究,使用Aquamin®-一种富含钙,镁,微量元素的多矿物质产品,源自红色海洋藻类作为干预。单独使用钙作为比较物。方法:招募了30名有结直肠癌风险的受试者,随机接受Aquamin®或单独钙治疗(每人每天提供800毫克钙)或安慰剂。在干预前后90天分别进行结肠活检。我们使用来自同一受试者的组织学上正常的结肠组织(基线),在结肠体培养中繁殖。一旦建立和扩大,我们使用相同的干预措施为期两周,并将反应(1.5mM)与干预90天后进行的人类结肠活检研究的结果进行比较。具体来说,通过定量免疫组织化学和基于串联质量标签质谱的蛋白质组学分析结肠镜组织和活检组织的生长和分化标志物。结果:在没有任何干预的情况下,正常组织结肠体的肉眼和显微镜外观以及细胞角蛋白20 (CK20)的表达均显示出高度分化。单独使用钙或Aquamin®时,CK20的表达仅略有增加。同样,CK20的表达在基线活检中较高,钙组的表达没有增加,但在干预90天后,Aquamin®组的表达增加了5%。在蛋白质组学筛选中,两种干预措施在1.5mM时,CK20在结肠组织中的表达增加了40%,而在结肠活检中,钙和Aquamin®的CK20表达分别增加了10%和21%。当对结肠体进行Ki67(生长标志物)表达评估时,与对照组相比,单独钙和Aquamin®分别降低了17.2%和18.4%。干预90天后的结肠活检分析显示,Aquamin®使Ki67的表达水平降低了20%,而单独使用钙则没有变化。在结肠样组织中,1.5mM处,钙和Aquamin®可使增殖细胞核抗原的差异蛋白组学表达降低32%和39%,而在结肠活检中,钙和Aquamin®可使Ki67蛋白分别降低4%和22%。结论:结肠镜培养维持的结肠组织为临床试验中收集的人体组织提供了良好的替代品。它可以用来评估个性化的响应,或者在相对较短的时间内提供响应的快速快照。差异蛋白质组学表达似乎比定量免疫组织化学更敏感。事实证明,钙和其他微量元素的组合在改变分化和生长标志物方面比单独钙更有效。引文格式:Muhammad N. Aslam, Shannon McClintock, Mohamed Ali H Jawad-Makki, Karsten Knuver, Daniyal M. Nadeem, Haris Ahmad, Durga Attili, Danielle (Kim) Turgeon, James Varani。人类结肠上皮细胞分化和生长控制:比较临床试验结果与人类结肠样细胞培养反应[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr LB220。
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Abstract LB220: Cellular Differentiation and Growth Control in the Human Colonic epithelium: Comparing Clinical Trial Outcomes to Responses in Human Colonoid Culture
Introduction: As part of our effort to understand the role of trace elements in colon polyp chemoprevention, we have conducted both colonoid culture (ex vivo) and human subject (in vivo) studies using Aquamin®— a calcium-, magnesium-, trace elements-rich, multi-mineral product derived from red marine algae as an intervention. Calcium alone was used as a comparator. Methods: Thirty subjects at-risk for colorectal cancer were enrolled and randomized to receive Aquamin® or calcium alone (each providing 800-mg calcium per day) or placebo. Colon biopsies were obtained before and after 90 days of intervention. We employed histologically normal colonic tissue from the same subjects (at baseline), to propagate in colonoid culture. Once established and expanded, we used the same interventions for a period of two weeks and compared the response (at 1.5mM) to the outcome of the studies conducted in human colonic biopsies after 90 days of intervention. Specifically, colonoid tissue and biopsies were subjected to analysis for markers of growth and differentiation by quantitative immunohistochemistry and tandem mass tag mass spectrometry-based proteomics. Results: The normal tissue colonoids demonstrated a high degree of differentiation as indicated by gross and microscopic appearance, and cytokeratin 20 (CK20) expression without either intervention. Only modest increases were seen in the CK20 expression with either calcium alone or Aquamin®. Similarly, CK20 expression was higher in baseline biopsies and there was no increase in the expression with calcium but a 5% increase seen with Aquamin® after 90 days of intervention. On proteomic screen, CK20 expression was increased by 40% in colonoid tissue in response to both interventions at 1.5mM, while CK20 expression increased by 10% and 21% with Calcium and Aquamin® in colon biopsies. When the colonoids were assessed for Ki67 (growth marker) expression, it was decreased by 17.2% and 18.4% with calcium alone and Aquamin® respectively as compared to the control. Analyzing colon biopsies after 90 days of intervention revealed that Aquamin® reduced the level of Ki67 expression by 20%, while no change was seen with calcium alone. Differential proteomic expression of proliferating cell nuclear antigen was decreased by 32% and 39% by calcium and Aquamin® at 1.5mM in colonoid tissue, whereas Ki67 protein was decreased by 4% and 22% with calcium and Aquamin®, respectively in colon biopsies. Conclusion: Colon tissue maintained in colonoid culture, thus, provides a good surrogate for human tissue collected in a clinical trial. It can be used to assess personalized responses or can provide a quick snapshot of the response in a relatively short time. Differential proteomic expression appears to be more sensitive than quantitative immunohistochemistry. A combination of calcium and additional trace elements proved to be more effective than calcium alone in altering differentiation and growth markers in either setting. Citation Format: Muhammad N. Aslam, Shannon McClintock, Mohamed Ali H Jawad-Makki, Karsten Knuver, Daniyal M. Nadeem, Haris Ahmad, Durga Attili, Danielle (Kim) Turgeon, James Varani. Cellular Differentiation and Growth Control in the Human Colonic epithelium: Comparing Clinical Trial Outcomes to Responses in Human Colonoid Culture [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr LB220.
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