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生物行为调节卵巢癌外泌体转录组。

Biobehavioral modulation of the exosome transcriptome in ovarian carcinoma.

机构信息

Department of Psychological and Brain Sciences, University of Iowa, Iowa City, Iowa.

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Iowa, Iowa City, Iowa.

出版信息

Cancer. 2018 Feb 1;124(3):580-586. doi: 10.1002/cncr.31078. Epub 2017 Nov 7.

Abstract

BACKGROUND

Social factors in the patient macroenvironment have been shown to influence molecular events in the tumor microenvironment and thereby influence cancer progression. However, biomarkers providing a window into the longitudinal effects of biobehavioral factors on tumor biology over time are lacking. Exosome analysis is a novel strategy for in vivo monitoring of dynamic changes in tumor cells. This study examined exosomal profiles from patients with low or high levels of social support for epithelial-mesenchymal transition (EMT) polarization and gene expression related to inflammation and β-adrenergic signaling.

METHODS

Exosomes were isolated from plasma sampled from a series of 40 women before primary surgical resection of advanced-stage, high-grade ovarian carcinoma. Samples were selected for analysis on the basis of extremes of low and high levels of social support. After exosomal isolation and RNA extraction, a microarray analysis of the transcriptome was performed.

RESULTS

Primary analyses identified significant upregulation of 67 mesenchymal-characteristic gene transcripts and downregulation of 63 epithelial-characteristic transcripts in patients with low social support; this demonstrated increased EMT polarization (P = .0002). Secondary analyses using promoter sequence bioinformatics supported a priori hypotheses linking low social support to 1) increased activity of cyclic adenosine monophosphate response element binding protein (CREB)/activating transcription factor (ATF) family transcription factors that mediate the β-adrenergic response to catecholamines via the cyclic adenosine monophosphate/protein kinase A signaling pathway (mean fold change for CREB: 2.24 ± 0.65; P = .0019; mean fold change for ATF: 2.00 ± 0.55; P = .0049) and 2) increased activity of the proinflammatory nuclear factor κB/Rel family of transcription factors (mean fold change: 2.10 ± 0.70; P = .0109).

CONCLUSIONS

These findings suggest the possibility of leveraging exosomes as a noninvasive assessment of biobehavioral factors to help to direct personalized treatment approaches. Cancer 2018;124:580-6. © 2017 American Cancer Society.

摘要

背景

患者宏观环境中的社会因素已被证明会影响肿瘤微环境中的分子事件,从而影响癌症的进展。然而,目前缺乏能够提供一个窗口来观察生物行为因素对肿瘤生物学随时间变化的纵向影响的生物标志物。外泌体分析是一种用于实时监测肿瘤细胞动态变化的新策略。本研究检测了社会支持水平低或高的上皮-间充质转化(EMT)极化患者的外泌体谱,以及与炎症和β-肾上腺素能信号相关的基因表达。

方法

从 40 名接受高级别卵巢癌初次手术切除的女性患者的术前血浆中分离出外泌体。根据社会支持水平的高低,选择样本进行分析。在外泌体分离和 RNA 提取后,进行了转录组的微阵列分析。

结果

初步分析发现,社会支持水平低的患者中有 67 个间充质特征基因转录本显著上调,63 个上皮特征转录本下调;这表明 EMT 极化增加(P = .0002)。使用启动子序列生物信息学的二次分析支持了先前的假设,即低社会支持与 1)通过环磷酸腺苷/蛋白激酶 A 信号通路介导儿茶酚胺的β-肾上腺素能反应的环磷酸腺苷反应元件结合蛋白(CREB)/激活转录因子(ATF)家族转录因子的活性增加有关(CREB 的平均倍数变化:2.24 ± 0.65;P = .0019;ATF 的平均倍数变化:2.00 ± 0.55;P = .0049),2)促炎核因子κB/Rel 家族转录因子的活性增加(平均倍数变化:2.10 ± 0.70;P = .0109)。

结论

这些发现表明,利用外泌体作为生物行为因素的非侵入性评估方法具有一定的可能性,有助于指导个性化的治疗方法。癌症 2018;124:580-6。© 2017 美国癌症协会。

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