School of Nursing, University of California, 2 Koret Way - N631Y, San Francisco, CA 94143-0610, USA.
School of Pharmacy and Pharmaceutical Sciences, University of California Irvine, 147B Bison Modular, Irvine, CA 92697, USA.
Cytokine. 2021 Dec;148:155653. doi: 10.1016/j.cyto.2021.155653. Epub 2021 Aug 10.
Cancer-related cognitive impairment (CRCI) is a significant problem for patients receiving chemotherapy. While a growing amount of pre-clinical and clinical evidence suggests that inflammatory mechanisms underlie CRCI, no clinical studies have evaluated for associations between CRCI and changes in gene expression. Therefore, the purpose of this study was to evaluate for differentially expressed genes and perturbed inflammatory pathways across two independent samples of patients with cancer who did and did not report CRCI. The Attentional Function Index (AFI) was the self-report measure used to assess CRCI. AFI scores of <5 and of >7.5 indicate low versus high levels of cognitive function, respectively. Of the 185 patients in Sample 1, 49.2% had an AFI score of <5 and 50.8% had an AFI score of >7.5. Of the 158 patients in Sample 2, 50.6% had an AFI score of <5 and 49.4% had an AFI score of >7.5. Data from 182 patients in Sample 1 were analyzed using RNA-seq. Data from 158 patients in Sample 2 were analyzed using microarray. Twelve KEGG signaling pathways were significantly perturbed between the AFI groups, five of which were signaling pathways related to inflammatory mechanisms (e.g., cytokine-cytokine receptor interaction, tumor necrosis factor signaling). This study is the first to describe perturbations in inflammatory pathways associated with CRCI. Findings highlight the role of cytokines both in terms of cytokine-specific pathways, as well as pathways involved in cytokine production and cytokine activation. These findings have the potential to identify new targets for therapeutics and lead to the development of interventions to improve cognition in patients with cancer.
癌症相关认知障碍 (CRCI) 是接受化疗的患者面临的一个重大问题。虽然越来越多的临床前和临床证据表明炎症机制是 CRCI 的基础,但尚无临床研究评估 CRCI 与基因表达变化之间的关联。因此,本研究旨在评估两个独立的癌症患者样本中差异表达的基因和受干扰的炎症途径,这些患者报告了或没有报告 CRCI。注意力功能指数 (AFI) 是用于评估 CRCI 的自我报告测量。AFI 评分<5 和>7.5 分别表示认知功能低和高。在样本 1 中的 185 名患者中,49.2%的 AFI 评分<5,50.8%的 AFI 评分>7.5。在样本 2 中的 158 名患者中,50.6%的 AFI 评分<5,49.4%的 AFI 评分>7.5。使用 RNA-seq 分析了样本 1 中 182 名患者的数据。使用微阵列分析了样本 2 中 158 名患者的数据。在 AFI 组之间,有 12 个 KEGG 信号通路受到显著干扰,其中 5 个是与炎症机制相关的信号通路(例如,细胞因子-细胞因子受体相互作用、肿瘤坏死因子信号)。本研究首次描述了与 CRCI 相关的炎症途径的干扰。研究结果强调了细胞因子在细胞因子特异性途径以及细胞因子产生和细胞因子激活途径中的作用。这些发现有可能确定新的治疗靶点,并开发改善癌症患者认知的干预措施。