PO.MCB10.01 · 分子与细胞生物学

短期术前热量限制下调乳腺癌和前列腺癌患者的 miR-21 并调节肠道微生物组

Short-term pre-operative caloric restriction downregulates miR-21 and modulates gut microbiome in breast cancer and prostate cancer patients

编号 2041 展板 1 时间 4/20 09:00–12:00 区域 Section 25 主讲 Meera Gupta, BS
分会场 MicroRNAs as Cancer Biomarkers, Therapeutic Targets, and Modulators of Treatment Response
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作者与单位 Authors & Affiliations

Meera Gupta1, Anuradha A. Shastri1, Pramila Anne1, Tiziana DeAngelis1, Leonard G. Gomella2, Adeseye Adekeye1, Melissa Lazar1, Nicole L. Simone1

1Thomas Jefferson University Sidney Kimmel Medical College, Philadelphia, PA,2Thomas Jefferson University, Philadelphia, PA

摘要 Abstract

中文摘要
目的:众多研究表明热量限制(CR)可改善肿瘤学标志物,但其调节临床结局的机制和程度仍备受关注。在本研究中,我们试图确定 2-5 周术前 CR 干预对致癌微小 RNA miR-21 以及乳腺癌和前列腺癌患者其他临床、微生物组和代谢标志物的影响。我们假设热量限制会降低 miR-21 介导的炎症,从而诱导患者特征的有利转变并增强抗肿瘤反应。 方法:从一所大型学术医学中心招募乳腺癌和前列腺癌患者,在确定性手术前最多 12 周参与热量减少 25% 的饮食干预。通过饮食日记、定期随访以及营养和行为咨询来维持依从性。在干预前后收集临床化验、体重、身体成分、生物标志物和微生物组样本。使用配对 t 检验来识别有显著意义的临床参数。微生物组数据使用 QIIME2 分析,微生物组途径分析使用 PiCrust2 进行。 结果:从 2016 年 8 月至 2018 年 10 月,35 名患者入组研究并完成了术前 CR 干预,平均持续 21 天。该干预导致显著的体重减轻,平均减轻 7.8 磅(p<0.0001)。患者疲劳程度降低,以 Promis 疲劳量表测量(p < 0.01)。瘦素(Leptin,n=23)和 IGFBP-3(n=25)均显著降低(p<0.05)。发现 miR-21 表达在干预后显著下调(p<0.05)。微生物组分析未发现 alpha 或 beta 多样性的任何显著差异。Picrust2 分析揭示了 10 条差异表达的功能性微生物组途径,其中变化最大的三条是苯甲酰-CoA 降解减少、L-阿拉伯糖降解 IV 减少和糖原降解减少。血清生物标志物微阵列分析揭示,在乳腺癌患者中,干预后 Eotaxin 2 和 IP 10 趋化因子显著下调(FDR < 0.05),在前列腺癌患者中,IGFBP-1 显著上调(FDR < 0.05)。 结论:本研究表明,短期术前热量限制是可行的,并在乳腺癌和前列腺癌患者中引发快速的生物学变化,包括致癌 miR-21 的显著下调和炎症性趋化因子的调节。微生物组途径和菌群的转变提示干预期间宿主/微生物组的协调适应。这些发现支持 CR 作为一种低风险的短期干预,值得进一步研究以确定其对长期肿瘤结局的潜在影响。
查看英文原文 English abstract
Purpose: Calorie restriction (CR) has been shown to improve oncological markers in numerous studies, the mechanism and extent to which it can modulate clinical outcomes remain of interest. In this study, we sought to determine the effect of a 2-5-week preoperative CR intervention on the oncogenic microRNA miR-21, as well as other clinical, microbiome and metabolic markers in patients with breast cancer and prostate cancer. We hypothesized that caloric restriction would lower miR-21-mediated inflammation, inducing a favorable shift in patient characteristics and enhancing anti-tumor responses. Methods: Breast cancer and prostate cancer patients from a large academic medical center were recruited to participate in a 25% reduced calorie diet intervention up to 12 weeks before definitive surgery. Adherence was maintained via a diet journal, regular check-ins, as well as nutritional and behavioral counseling. Clinical labs, weight, body composition, biomarkers and microbiome samples were collected pre and post-intervention. Paired t-tests were used to identify significant clinical parameters. Microbiome data was analyzed with QIIME2 and microbiome pathway analysis was conducted with PiCrust2. Results: From August 2016 to October 2018, 35 patients enrolled in the study and completed the pre-operative CR intervention, lasting an average of 21 days. The intervention resulted in significant weight loss, with an average of 7.8 pounds lost (p<0.0001). Patient fatigue was decreased, as measured by the Promis Fatigue scale (p < 0.01). Leptin (n=23) and IGFBP-3 (n=25) were both significantly decreased (p<0.05). MiR-21 expression was found to be significantly downregulated post-intervention (p<0.05). Microbiome analysis did not find any significant differences in alpha or beta diversity. Picrust2 analysis revealed 10 differentially expressed functional microbiome pathways, with the three greatest changes being decreased benzoyl-CoA degradation, decreased L-arabinose degradation IV, and decreased glycogen degradation. Serum biomarker microarray analysis revealed significantly post-intervention downregulation of Eotaxin 2 and IP 10 chemokines in breast cancer patients (FDR < 0.05), and significant upregulation of IGFBP-1 in prostate cancer patients (FDR < 0.05). Conclusions: This study demonstrates that short term preoperative caloric restriction is feasible and elicits rapid biologic changes in breast and prostate cancer patients, including significant downregulation of the oncogenic miR-21 and modulation of inflammatory chemokines. Microbiome pathway and taxa shifts suggest coordinated host/microbiome adaptation during the intervention. These findings support CR as a low-risk short-term intervention that warrants further investigation to determine the potential impact on long-term cancer outcomes.
利益披露 Disclosure
M. Gupta, None.. A. A. Shastri, None.. P. Anne, None.. T. DeAngelis, None.. A. Adekeye, None.. M. Lazar, None.. N. L. Simone, None.

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