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Altered time structure of neuro-endocrine-immune system function in lung cancer patients

机译:肺癌患者神经内分泌免疫系统功能的时间结构改变

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Background The onset and the development of neoplastic disease may be influenced by many physiological, biological and immunological factors. The nervous, endocrine and immune system might act as an integrated unit to mantain body defense against this pathological process and reciprocal influences have been evidenced among hypothalamus, pituitary, thyroid, adrenal, pineal gland and immune system. In this study we evaluated differences among healthy subjects and subjects suffering from lung cancer in the 24-hour secretory profile of melatonin, cortisol, TRH, TSH, FT4, GH, IGF-1 and IL-2 and circadian variations of lymphocyte subpopulations. Methods In ten healthy male volunteers (age range 45-66) and ten male patients with untreated non small cell lung cancer (age range 46-65) we measured melatonin, cortisol, TRH, TSH, FT4, GH, IGF-1 and IL-2 serum levels and percentages of lymphocyte subpopulations on blood samples collected every four hours for 24 hours. One-way ANOVA between the timepoints for each variable and each group was performed to look for a time-effect, the presence of circadian rhythmicity was evaluated, MESOR, amplitude and acrophase values, mean diurnal levels and mean nocturnal levels were compared. Results A clear circadian rhythm was validated in the control group for hormone serum level and for lymphocyte subsets variation. Melatonin, TRH, TSH, GH, CD3, CD4, HLA-DR, CD20 and CD25 expressing cells presented circadian rhythmicity with acrophase during the night. Cortisol, CD8, CD8bright, CD8dim, CD16, TcRδ1 and δTcS1 presented circadian rhythmicity with acrophase in the morning/at noon. FT4, IGF-1 and IL-2 variation did not show circadian rhythmicity. In lung cancer patients cortisol, TRH, TSH and GH serum level and all the lymphocyte subsubsets variation (except for CD4) showed loss of circadian rhythmicity. MESOR of cortisol, TRH, GH, IL-2 and CD16 was increased, whereas MESOR of TSH, IGF-1, CD8, CD8bright, TcRδ1 and δTcS1 was decreased in cancer patients. The melatonin/cortisol mean nocturnal level ratio was decreased in cancer patients. Conclusion The altered secretion and loss of circadian rhythmicity of many studied factors observed in the subjects suffering from neoplastic disease may be expression of gradual alteration of the integrated function of the neuro-immune-endocrine system
机译:背景肿瘤疾病的发生和发展可能受到许多生理,生物学和免疫学因素的影响。神经,内分泌和免疫系统可能是维持机体抵抗这种病理过程的综合单元,并且在下丘脑,垂体,甲状腺,肾上腺,松果体和免疫系统之间存在相互影响。在这项研究中,我们评估了健康受试者和罹患肺癌的受试者在褪黑激素,皮质醇,TRH,TSH,FT4,GH,IGF-1和IL-2的24小时分泌谱以及淋巴细胞亚群昼夜变化方面的差异。方法在十位健康的男性志愿者(年龄范围为45-66岁)和十位男性未治疗的非小细胞肺癌患者(年龄范围为46-65岁)中,我们测量了褪黑激素,皮质醇,TRH,TSH,FT4,GH,IGF-1和IL每4小时收集一次血清中的-2血清水平和淋巴细胞亚群百分比,持续24小时。在每个变量和每个组的时间点之间进行单向方差分析以寻找时间效应,评估昼夜节律的存在,比较MESOR,振幅和顶相值,平均昼夜水平和平均夜间水平。结果对照组的激素血清水平和淋巴细胞亚群变异均证实有清晰的昼夜节律。褪黑素,TRH,TSH,GH,CD3,CD4,HLA-DR,CD20和CD25表达细胞在夜间呈现昼夜节律性并伴有前肢相。早晨/中午,皮质醇,CD8,CD8 ,CD8 dim ,CD16,TcRδ1和δTcS1表现为昼夜节律性并伴有顶峰相。 FT4,IGF-1和IL-2变异未显示昼夜节律。在肺癌患者中,皮质醇,TRH,TSH和GH血清水平以及所有淋巴细胞亚群变异(CD4除外)均显示出昼夜节律性丧失。癌症患者的皮质醇,TRH,GH,IL-2和CD16的MESOR升高,而TSH,IGF-1,CD8,CD8 ,TcRδ1和δTcS1的MESOR降低。癌症患者的褪黑素/皮质醇平均夜间水平比降低。结论在患有肿瘤疾病的受试者中观察到的许多研究因素的昼夜节律性分泌和丧失可能是神经-免疫-内分泌系统综合功能的逐渐表达。

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