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疏肝健脾方对髓源性抑制细胞介导的抑郁乳腺癌小鼠的影响。 (括号内内容缺失,你可补充完整后继续让我翻译)

Effects of Shugan Jianpi Formula () on myeloid-derived suppression cells-mediated depression breast cancer mice.

作者信息

Lu Yu-Tong, Li Jie, Qi Xin, Pei Ying-Xia, Shi Wen-Guang, Lin Hong-Sheng

机构信息

Department of Oncology, Guang'anmen Hospital, China Academy of Chinese Medicine Sciences, Beijing, 100053, China.

Department of Oncology, Southern District of Guang'anmen Hospital, China Academy of Chinese Medicine Sciences, Beijing, 102600, China.

出版信息

Chin J Integr Med. 2017 Jun;23(6):453-460. doi: 10.1007/s11655-016-2734-4. Epub 2016 Oct 28.

Abstract

OBJECTIVE

To observe the intervention effect of Shugan Jianpi Formula (, SGJPF) on a breast cancer mouse model with depression and investigate the underlying mechanism of SGJPF in preventing the development of breast cancer.

METHODS

The breast cancer model was induced by inoculation of breast cancer cells, the depression model was induced by chronic stress stimuli, and the depression cancer model was established by combining the two factors. The mice were divided into 7 groups: normal control, depression model, tumor model, depression tumor model, SGJPF, chemotherapy, and SGJPF+chemotherapy groups. The last 3 groups were depression breast cancer mice and treated respectively with SGJPF, chemotherapy drug gemcitabine (GEM), and SGJPF alongside GEM. The condition of the mice was evaluated by the expression of 5-hydroxytryptamine in hippocampus after the sucrose water test and open field test, weight change, and survival time. Tumor growth was monitored with in vivo imaging. Flow cytometry was used to analyze the level of myeloid-derived suppression cell (MDSC) in the mouse spleen, T cell subsets, and the early apoptosis of CD8 T cells.

RESULTS

The SGJPF+GEM group had the highest inhibition rate and the longest survival time (P<0.01). The MDSC level and the apoptosis rate of CD8 T cells was the highest in the SGJPF+GEM group (P<0.05).

CONCLUSIONS

Depressive disorders and tumor growth could suppress the immune function of mice to different degrees, and the microenvironment in late 4T1 inflammatory breast cancer may play an important role in the pathological process. SGJYF could regulate the immune microenvironment by reducing CD8 T lymphocyte apoptosis and tumor cell activity, increasing immune surveillance capability, and inhibiting MDSC proliferation, thus prolonging the survival time of tumor-bearing mice.

摘要

目的

观察疏肝健脾方(SGJPF)对乳腺癌伴抑郁小鼠模型的干预作用,并探讨其预防乳腺癌发生发展的潜在机制。

方法

通过接种乳腺癌细胞诱导乳腺癌模型,采用慢性应激刺激诱导抑郁模型,将二者结合建立抑郁-癌模型。将小鼠分为7组:正常对照组、抑郁模型组、肿瘤模型组、抑郁-肿瘤模型组、疏肝健脾方组、化疗组、疏肝健脾方+化疗组。后3组为抑郁性乳腺癌小鼠,分别给予疏肝健脾方、化疗药物吉西他滨(GEM)以及疏肝健脾方联合GEM治疗。通过蔗糖水试验和旷场试验后海马中5-羟色胺的表达、体重变化和生存时间评估小鼠状况。采用体内成像监测肿瘤生长。运用流式细胞术分析小鼠脾脏中髓源性抑制细胞(MDSC)水平、T细胞亚群以及CD8⁺T细胞的早期凋亡情况。

结果

疏肝健脾方+GEM组抑制率最高,生存时间最长(P<0.01)。疏肝健脾方+GEM组MDSC水平和CD8⁺T细胞凋亡率最高(P<0.05)。

结论

抑郁障碍和肿瘤生长可不同程度抑制小鼠免疫功能,4T1炎性乳腺癌晚期的微环境可能在病理过程中起重要作用。疏肝健脾方可通过减少CD8⁺T淋巴细胞凋亡和肿瘤细胞活性、增强免疫监视能力、抑制MDSC增殖来调节免疫微环境,从而延长荷瘤小鼠的生存时间。

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