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一种新的草药配方 KSG-002,通过靶向巨噬细胞中 NF-κB 依赖性 TNFα 的产生来抑制乳腺癌的生长和转移。

A New Herbal Formula, KSG-002, Suppresses Breast Cancer Growth and Metastasis by Targeting NF- κ B-Dependent TNF α Production in Macrophages.

机构信息

Laboratory of Clinical Biology and Pharmacogenomics, Department of Preventive Medicine, Kyung Hee University, 1 Hoegi, Seoul 130-701, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2013;2013:728258. doi: 10.1155/2013/728258. Epub 2013 May 30.

Abstract

Tumor-associated macrophages (TAMs) in tumor microenvironment regulate cancer progression and metastases. In breast cancer, macrophage infiltration is correlated with a poor prognosis. While metastatic breast cancer is poor prognostic with a severe mortality, therapeutic options are still limited. In this study, we demonstrate that KSG-002, a new herbal composition of radices Astragalus membranaceus and Angelica gigas, suppresses breast cancer via inhibiting TAM recruitment. KSG-002, an extract of radices Astragalus membranaceus and Angelica gigas at 3 : 1 ratio, respectively, inhibited MDA-MB-231 xenograft tumor growth and pulmonary metastasis in nude mice, while KSG-001, another composition (1 : 1 ratio, w/w), enhanced tumor growth, angiogenesis, and pulmonary metastasis, in vivo. KSG-002 further decreased the infiltrated macrophage numbers in xenograft tumor cohorts. In Raw264.7 cells, KSG-002 but not KSG-001 inhibited cell proliferation and migration and reduced TNF-alpha (TNF α ) production by inhibiting NF- κ B pathway. Furthermore, a combinatorial treatment of KSG-002 with TNF α inhibited a proliferation and migration of both MDA-MB-231 and Raw264.7 cells. Taken together, we conclude that KSG-002 suppresses breast cancer growth and metastasis through targeting NF- κ B-mediated TNF α production in macrophages.

摘要

肿瘤相关巨噬细胞(TAMs)在肿瘤微环境中调节癌症的进展和转移。在乳腺癌中,巨噬细胞浸润与预后不良相关。转移性乳腺癌预后不良,死亡率高,但治疗选择仍然有限。在这项研究中,我们证明了 KSG-002,一种新的黄芪和当归草药组合物,通过抑制 TAM 募集来抑制乳腺癌。KSG-002 是黄芪和当归提取物的 3:1 比例混合物,分别抑制 MDA-MB-231 异种移植肿瘤生长和裸鼠肺转移,而 KSG-001 是另一种组成物(1:1 比例,w/w),增强肿瘤生长、血管生成和肺转移,体内。KSG-002 进一步减少了异种移植肿瘤队列中浸润的巨噬细胞数量。在 Raw264.7 细胞中,KSG-002 而非 KSG-001 抑制细胞增殖和迁移,并通过抑制 NF- κ B 通路减少 TNF-α(TNF α )的产生。此外,KSG-002 与 TNF α 的联合治疗抑制了 MDA-MB-231 和 Raw264.7 细胞的增殖和迁移。总之,我们得出结论,KSG-002 通过靶向 NF- κ B 介导的巨噬细胞中 TNF α 的产生来抑制乳腺癌的生长和转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16ad/3683439/d5d1fa542087/ECAM2013-728258.001.jpg

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