Electroacupuncture promotes apoptosis and inhibits axonogenesis by activating p75 neurotrophin receptor for triple-negative breast xenograft in mice

被引:4
作者
Tian, Yehong [1 ,2 ]
Qiu, Xiaowei [1 ,4 ]
Qi, Xuewei [1 ]
Dong, Zhenzhen [1 ]
Zhao, Jianxin [1 ]
Huang, Jinchang [1 ,3 ]
Jiang, Xin [1 ,3 ]
机构
[1] Beijing Univ Chinese Med, Affiliated Hosp 3, Beijing, Peoples R China
[2] Shaanxi Univ Chinese Med, Inst Acupuncture & Moxibust, Xianyang, Shaanxi, Peoples R China
[3] Beijing Univ Chinese Med, Inst Acupuncture & Moxibust Canc Care, Xianyang, Peoples R China
[4] BeiJing Chaoyang Intergrat Med Emergency Med Ctr, Beijing, Peoples R China
关键词
Electroacupuncture; Breast cancer; Apoptosis; P75NTR; Axonogenesis; NERVE GROWTH-FACTOR; CELL-DEATH; PROLIFERATION; PROTEIN; P75(NTR); SUPPRESSES; EXPRESSION; SURVIVAL; INVASION; NGF;
D O I
10.1016/j.jchemneu.2022.102133
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: The aim of this study was to investigate the anti-tumor effect of electroacupuncture (EA) on mice bearing breast tumors by regulating p75 neurotrophin receptor (p75NTR) and remodelling intratumoral innervation. Methods: Female BALB/c mice were implanted with 4T1 breast tumor cells to establish a murine mammary cancer model. Tumor volume and weight were measured to evaluate tumor growth. Cell apoptosis was assessed by TUNEL assay. The relative expression of p75NTR, TrkA, TrkB, NGF and proNGF were detected by immunohistochemistry. Neurotransmitter and neurotrophin were detected by enzyme-linked immunosorbent assay. Intratumoral innervation was confirmed by beta 3-tubulin and TH labeling immunohistochemistry. The antagonist TAT-Pep5 was employed to determine if the effects of EA on tumor growth and cell apoptosis were mediated by p75NTR. Results: Peritumoral EA alleviated tumor growth especially after 14 days of intervention. Apoptosis index in the tumor tissue was obviously decreased after EA. Meanwhile, EA intervention significantly upregulated the expression of p75NTR and proNGF, along with a decline in the tumor growth and an increase in the cell apoptosis. Besides, EA reduced local sympathetic innervation and downregulated sympathetic neurotransmitter NE level in the local tumor. Furthermore, p75NTR antagonist alleviated EA-mediated cell apoptosis and intratumoral innervation. Conclusions: One mechanism of EA intervention for alleviating tumor progression is mediated by p75NTR to promote apoptosis and decrease intratumoral axonogenesis in the tumor microenvironment.
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页数:13
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