The level of oxidative stress and the expression of genes involved in DNA-damage signaling pathways in depressive patients with colorectal carcinoma

被引:36
作者
Wei, Yong-chang [1 ]
Zhou, Fu-ling [2 ]
He, Da-lin [1 ]
Bai, Ji-rong [3 ]
Hui, Ling-yun [1 ]
Wang, Xin-yang [1 ]
Nan, Ke-jun [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Clin Oncol, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Clin Hematol & Oncol, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Gen Surg, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorectal carcinoma; Depression; Oxidative stress; HAMD; DNA damaged; 8-hydroxy-deoxyguanosine; Gene expression; p34; HRAD51; QUALITY-OF-LIFE; CANCER-PATIENTS; MAJOR DEPRESSION; TUMOR-SUPPRESSOR; BREAST-CANCER; NITRIC-OXIDE; FEASIBILITY; GLUTATHIONE; ADJUSTMENT; DISORDERS;
D O I
10.1016/j.jpsychores.2008.09.001
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objectives: This study investigated the connection among the oxidative stress, depression and expression of specific genes involved in DNA-damage signaling pathways in patients with colorectal carcinoma (CRC). Methods: A unique Dukes'C subset of patients with newly diagnosed colorectal adenocarcinoma were assessed using the Hamilton Depression Rating Scale (HAMD), Zung Self-rating Depression Scale (SDS), Zung Self-rating Anxiety Scale (SAS), Symptom Checklist 90 (SCL-90) and other multiple-item questionnaires. Oxidative-stress-related parameters in sera and the expression of genes were monitored during a pretreatment period. Results: Eighty-two eligibility cases were divided into 2 groups based on an HAMD score cutoff of 20: the mean score was 28.29 in Group A (depression, n=52) and 16.50 in Group B (nondepression, n=30). The serum total antioxidant capacity, catalase, and superoxide dismutase concentrations were lower in Group A, whereas those of nitric oxide and malondialdehyde were higher in Group A. Importantly, the 8-hydroxy-deoxyguanosine level was higher in Group A than in Group B (P<.05). Microarray analysis revealed that the expressions of p34, PA26, and ABL were higher in Group A, whereas those of HRAD51, CR6, and XRCC3 were higher in Group B. Conclusion: Oxidative stress is capable of causing neuronal toxicity via lipid peroxidation, DNA damage, and abnormalities of gene expression, and therefore is a possible pathogenic mechanism underlying depression in patients with CRC. Crown Copyright (c) 2009 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:259 / 266
页数:8
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