Whole genome gene expression changes and hematological effects of rikkunshito in patients with advanced non-small cell lung cancer receiving first line chemotherapy

被引:5
|
作者
Chen, Yung-Che [1 ,2 ]
Lin, An-Shen [1 ]
Hung, Yu-Chiang [3 ,4 ]
Chen, Kuang-Den [5 ,6 ]
Wu, Ching-Yuan [7 ]
Lie, Chien-Hao [1 ]
Hsiao, Chang-Chun [2 ]
Chen, Chung-Jen [8 ]
Liu, Shih-Feng [1 ]
Fang, Wen-Feng [1 ,9 ]
Chang, Jen-Chieh [2 ]
Wang, Ting-Ya [1 ]
Wang, Yi-Hsi [1 ]
Chung, Yu-Hsiu [1 ]
Chao, Tung-Ying [1 ]
Leung, Sum-Yee [1 ]
Su, Mao-Chang [1 ,9 ]
Lin, Meng-Chih [1 ]
机构
[1] Kaohsiung Chang Gung Mem Hosp, Div Pulm & Crit Care Med, 123 Ta Pei Rd, Kaohsiung 83301, Taiwan
[2] Kaohsiung Chang Gung Mem Hosp, Div Rheumatol, Kaohsiung 83301, Taiwan
[3] Kaohsiung Chang Gung Mem Hosp, Dept Chinese Med, Kaohsiung 83301, Taiwan
[4] Kaohsiung Chang Gung Mem Hosp, Sch Tradit Chinese Med, Kaohsiung 83301, Taiwan
[5] Kaohsiung Chang Gung Mem Hosp, Ctr Translat Res Biomed Sci, Kaohsiung 83301, Taiwan
[6] Chang Gung Univ, Coll Med, 123 Ta Pei Rd, Kaohsiung 83301, Taiwan
[7] Chiayi Chang Gung Mem Hosp, Dept Chinese Med, Chiayi 61361, Taiwan
[8] Chang Gung Univ, Grad Inst Clin Med Sci, Coll Med, Kaohsiung 83301, Taiwan
[9] Chang Gung Univ Technol, Dept Resp Care, Chiayi 61363, Taiwan
关键词
rikkunshito; non-small cell lung cancer; chemotherapy; microarray gene expression; neutropenia; CISPLATIN-INDUCED ANOREXIA; JUNCTIONAL ADHESION MOLECULE; INDUCED NEUTROPENIA; RECEPTOR EXPRESSION; PROGNOSTIC-FACTOR; MEDICINE; NEUTROPHILS; MANAGEMENT; PATHWAYS; MECHANISMS;
D O I
10.3892/etm.2017.4773
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
It has been demonstrated that the traditional Chinese medicine rikkunshito, ameliorates anorexia in several types of human cancer and attenuates lung injury by inhibiting neutrophil infiltration. The current study investigated the clinical and hematological effects of rikkunshito and its underlying mechanisms of action in the treatment of advanced non-small cell lung cancer (NSCLC). The Illumina microarray BeadChip was used to analyze the whole-genome expression profiles of peripheral blood mononuclear cells in 17 patients with advanced NSCLC. These patients were randomized to receive combination chemotherapy (cisplatin and gemcitabine) with (n=9, CTH+R group) or without (n=8, CTH group) rikkunshito. The primary endpoint was the treatment response and the categories of the scales of anorexia, nausea, vomiting and fatigue; secondary endpoints included the hematological effect and whole genome gene expression changes. The results of the current study indicated that there were no significant differences in clinical outcomes, including treatment response and toxicity events, between the two groups. Median one-year overall survival (OS) was 12 months in the CTH group and 11 months in the CTH+R group (P=0.058 by log-rank test), while old age (>60 years old) was the only independent factor associated with one-year OS (hazard ratio 1.095, 95% confidence interval, 1.09-1.189, P=0.030). Patients in the CTH+R group experienced significantly greater maximum decreases in both white cell count (P=0.034) and absolute neutrophil count (P=0.030) from the baseline. A total of 111 genes associated with neutrophil apoptosis, the cell-killing ability of neutrophils, natural killer cell activation and B cell proliferation were up-regulated following rikkunshito treatment. A total of 48 genes associated with neutrophil migration, coagulation, thrombosis and type I interferon signaling were down-regulated following rikkunshito treatment. Rikkunshito may therefore affect the blood neutrophil count when used with combination chemotherapy in patients with NSCLC, potentially by down-regulating prostaglandin-endoperoxidase synthase 1, MPL, AMICAI and junctional adhesion molecule 3, while up-regulating elastase, neutrophil expressed, proteinase 3, cathepsin G and cluster of differentiation 24.
引用
收藏
页码:2040 / 2052
页数:13
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