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巨噬细胞衍生的SPARC减轻M2介导的促肿瘤表型。

Macrophage-derived SPARC Attenuates M2-mediated Pro-tumour Phenotypes.

作者信息

Hu Jianwen, Ma Yongchen, Ma Ju, Chen Shanwen, Zhang Xiaoqian, Guo Shihao, Huang Zhihao, Yue Taohua, Yang Yanpeng, Ning Yingze, Zhu Jing, Wang Pengyuan, Wang Xin, Chen Guowei, Liu Yucun

机构信息

Department of General Surgery, Peking University First Hospital, Beijing, 100034, PR China.

Endoscopy Center, Peking University First Hospital, Beijing, 100034, PR China.

出版信息

J Cancer. 2020 Mar 4;11(10):2981-2992. doi: 10.7150/jca.39651. eCollection 2020.

DOI:10.7150/jca.39651
PMID:32226513
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7086259/
Abstract

Since the theory of seed and soil was put forward, people have increasingly recognized that the tumour microenvironment is an important regulator of tumour progression and therapeutic response. Among them, M2-type macrophages (M2, as the major macrophage subtype in the tumour foci) have important promoting effects on various biological behaviours. Secreted protein acidic and rich in cysteine (SPARC) is an important anti-tumour component in the microenvironment of gastric cancer. This study shows that macrophages are an important source of the SPARC and that SPARC overexpression in M2 can reduce M2-mediated promoting proliferation, migration and anti-apoptotic effects in gastric cancer. Additionally, the AKT/mTOR signalling pathways may participate in the malignant process.

摘要

自“种子与土壤”学说提出以来,人们越来越认识到肿瘤微环境是肿瘤进展和治疗反应的重要调节因子。其中,M2型巨噬细胞(M2是肿瘤病灶中的主要巨噬细胞亚型)对各种生物学行为具有重要的促进作用。富含半胱氨酸的酸性分泌蛋白(SPARC)是胃癌微环境中的一种重要抗肿瘤成分。本研究表明,巨噬细胞是SPARC的重要来源,M2中SPARC的过表达可降低M2介导的胃癌增殖、迁移促进作用及抗凋亡作用。此外,AKT/mTOR信号通路可能参与了这一恶性过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ee6/7086259/6eca641b5a0b/jcav11p2981g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ee6/7086259/4f274af6a577/jcav11p2981g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ee6/7086259/6eca641b5a0b/jcav11p2981g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ee6/7086259/4f274af6a577/jcav11p2981g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ee6/7086259/6eca641b5a0b/jcav11p2981g003.jpg

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本文引用的文献

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Low expression of SPARC in gastric cancer-associated fibroblasts leads to stemness transformation and 5-fluorouracil resistance in gastric cancer.胃癌相关成纤维细胞中SPARC的低表达导致胃癌的干性转化和5-氟尿嘧啶耐药。
Cancer Cell Int. 2019 May 21;19:137. doi: 10.1186/s12935-019-0844-8. eCollection 2019.
2
Macrophage ERα promoted invasion of endometrial cancer cell by mTOR/KIF5B-mediated epithelial to mesenchymal transition.巨噬细胞 ERα 通过 mTOR/KIF5B 介导向子宫内膜癌细胞的上皮间质转化促进侵袭。
Immunol Cell Biol. 2019 Jul;97(6):563-576. doi: 10.1111/imcb.12245. Epub 2019 Mar 14.
3
Dual role of macrophage in tumor immunity.
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Clin Cancer Res. 2023 Sep 1;29(17):3498-3513. doi: 10.1158/1078-0432.CCR-23-0219.
4
Tumor microenvironment-mediated immune tolerance in development and treatment of gastric cancer.肿瘤微环境介导的胃癌发生发展及治疗中的免疫耐受。
Front Immunol. 2022 Oct 20;13:1016817. doi: 10.3389/fimmu.2022.1016817. eCollection 2022.
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The matricellular protein SPARC induces inflammatory interferon-response in macrophages during aging.基质细胞蛋白 SPARC 在衰老过程中诱导巨噬细胞产生炎症性干扰素反应。
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