Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice
Back to article page
OriginalPaper|Updated:2021-08-27
|
Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice
Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice
中国结合医学杂志(英文版)2017年23卷第6期 页码:453-460
Affiliations:
1. Department of Oncology, Guang’anmen Hospital, China Academy of Chinese Medicine Sciences,Beijing,China
2. Department of Oncology, Southern District of Guang’anmen Hospital, China Academy of Chinese Medicine Sciences,Beijing,China
Author bio:
Funds:
Supported by the National Natural Science Foundation of China (No. 81273946 and No. 81072802) and the National Science and Technology Major Projects for "Major New Drugs Innovation and Development" (No. 2013ZX09303301)
Lu, Yt., Li, J., Qi, X. et al. Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice., Chin. J. Integr. Med. 23, 453–460 (2017). https://doi.org/10.1007/s11655-016-2734-4
Yu-tong Lu, Jie Li, Xin Qi, et al. Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice[J]. Chinese Journal of Integrative Medicine, 2017,23(6):453-460.
Lu, Yt., Li, J., Qi, X. et al. Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice., Chin. J. Integr. Med. 23, 453–460 (2017). https://doi.org/10.1007/s11655-016-2734-4DOI:
Yu-tong Lu, Jie Li, Xin Qi, et al. Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice[J]. Chinese Journal of Integrative Medicine, 2017,23(6):453-460. DOI: 10.1007/s11655-016-2734-4.
Effects of Shugan Jianpi Formula (疏肝健脾方) on myeloid-derived suppression cells-mediated depression breast cancer mice
摘要
To observe the intervention effect of Shugan Jianpi Formula (疏肝健脾方
SGJPF) on a breast cancer mouse model with depression and investigate the underlying mechanism of SGJPF in preventing the development of breast cancer. 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. 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). 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.
Abstract
To observe the intervention effect of Shugan Jianpi Formula (疏肝健脾方
SGJPF) on a breast cancer mouse model with depression and investigate the underlying mechanism of SGJPF in preventing the development of breast cancer. 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. 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). 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.
关键词
Breast CancerShugan Jianpi FormulaChinese Medicinemyeloid-derived suppression celldepressive disordersapoptosis
Keywords
Breast CancerShugan Jianpi FormulaChinese Medicinemyeloid-derived suppression celldepressive disordersapoptosis
references
Kenne Sarenmalm E, Ohlén J, Odén A, Gaston-Johansson F. Experience and predictors of symptoms, distress and health-related quality of life over time in postmenopausal women with recurrent breast cancer. Psychooncology 2008;17:497–505.
Okamura M, Yamawaki S, Akechi T, Taniguchi K, Uchitomi Y. Psychiatric disorders following first breast cancer recurrence: prevalence, associated factors and relationship to quality of life. Jpn J Clin Oncol 2005;35:302–309.
Jim HS, Small BJ, Minton S, Andrykowski M, Jacobsen PB. History of major depressive disorder prospectively predicts worse quality of life in women with breast cancer. Ann Behav Med 2012;43:402–408.
Zhang YR, Li J, Li L. An observation and analysis of the features of depressive disorder in the incidence and progression of breast cancer. Chin J Integr Tradit West Med (Chin) 2013;4:459–461.
Yang WC, Ma G, Chen SH, Pan PY. Polarization and reprogramming of myeloid-derived suppressor cells. J Mol Cell Biol 2013;5:207–209.
Gabrilovich DI, Bronte V, Chen SH, Colombo MP, Ochoa A, Ostrand-Rosenberg S, et al. The terminology issue for Myeloid-derived suppressor cells. Cancer Res 2007;67:425–426.
Bronte V, Zanovello P. Regulation of immune responses by L-arginine metabolism. Nat Rev Immunol 2005;5:641–654.
Youn JI, Nagaraj S, Collazo M, Gabrilovich DI. Subsets of myeloid-derived suppressor cells in tumor-bearing mice. J Immunol 2008;181:5791–5802.
Kusmartsev S, Gabrilovich DI. Role of immature myeloid cells in mechanisms of immune evasion in cancer. Cancer Immunol Immunother 2006;55:237–245.
Yang F, Zhang QY, Kang XM. Antiangiogenic effect of xeloda on 4T1 mammary cancer. Progr Modern Biomed (Chin) 2007;7:1294–1296.
Cumashi A, Tinari N, Rossi C, Lattanzio R, Natoli C, Piantelli M, et al. Sunitinib malate (SU-11248) alone or in combination with low-dose docetaxel inhibits the growth of DU-145 prostate cancer xenografts. Cancer Letters 2008;270:229–233.
Iijima M, Ito A. Pharmacological characterization of repeated corticosterone injection-induced depression model in rats. Brain Res 2010;9:75–80.
Juver JP, Vercosa N. Depression in patients with advanced cancer and pain. Rev Bras Anestesiol 2008;58:287–298.
Zhang Baozhong. Features of tumor patients accompanying anxiety-depression and clinical curative effect. J Clin Psychosom Dis (Chin) 2007;13:17–18.
Yang XL, Zhang CZ, Wei XQ, Liu JB. An analysis on risk factors of moderate-severe depression in patients with gynecologic malignancies. China Cancer (Chin) 2009;18:195–197.
Ochando C, Chen SH. Myeloid-derived suppressor cells in transplantation and cancer. Immunol Res 2012;54:275–285.
Reid I, Forbes N, Stewart C, Matthews K. Chronic mild stress and depressive disorder: a useful new model? Psychopharmacology (Berl) 1997;134:365–367, 371-377.
De Vry J, Schreiber R. The chronic mild stress depression model: future developments from a drug discovery perspective. Psychopharmacology (Berl) 1997;134:349–350, 371-377.
Green A D, Barr A M, Galea L A. Role of estradiol withdrawal in’ anhedonic’ sucrose consumption: a model of postpartum depression. Physiol Behav 2009;97:259–256.
Newberg AB, Amsterdam JD, Wintering N, Shults J. Low brain serotonin transporter binding in major depressive disorder. Psychiatry Res 2012;202:161–167.
Nagaraj S, Gabrilovich DI. Tumor escape mechanism governed by myeloid-derived suppressor cells. Cancer Res 2008;68:561–563.
Ostrand-Rosenberg S, Sinha P, Beury DW, Clements VK. Cross-talk between myeloid-derived suppressor cells (MDSC), macrophages, and dendritic cells enhances tumor-induced immune suppression. Semin Cancer Biol 2012;22:275–281.