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解析中国灵芝甘露聚糖 GSBP-2 的结构及其对三阴性乳腺癌迁移和侵袭的影响。

Structural clarification of mannoglucan GSBP-2 from Ganoderma sinense and its effects on triple-negative breast cancer migration and invasion.

机构信息

School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.

Department of Chinese Medicine, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, Guangdong, China.

出版信息

Int J Biol Macromol. 2024 Jun;269(Pt 1):131903. doi: 10.1016/j.ijbiomac.2024.131903. Epub 2024 Apr 28.

Abstract

Ganoderma sinense, known as Lingzhi in China, is a medicinal fungus with anti-tumor properties. Herein, crude polysaccharides (GSB) extracted from G. sinense fruiting bodies were used to selectively inhibit triple-negative breast cancer (TNBC) cells. GSBP-2 was purified from GSB, with a molecular weight of 11.5 kDa and a composition of α-l-Fucp-(1→, β-d-Glcp-(1→, β-d-GlcpA-(1→, →3)-β-d-Glcp-(1→, →3)-β-d-GlcpA-(1→, →4)-α-d-Galp-(1→,→6)-β-d-Manp-(1→, and →3,6)-β-d-Glcp-(1→ at a ratio of 1.0:6.3:1.7:5.5:1.5:4.3:8.0:7.9. The anti-MDA-MB-231 cell activity of GSBP-2 was determined by methyl thiazolyl tetrazolium, colony formation, scratch wound healing, and transwell migration assays. The results showed that GSBP-2 could selectively inhibit the proliferation, migration, and invasion of MDA-MB-231 cells through the regulation of genes targeting epithelial-mesenchymal transition (i.e., Snail1, ZEB1, VIM, CDH1, CDH2, and MMP9) in the MDA-MB-231 cells. Furthermore, Western blotting results indicated that GSBP-2 could restrict epithelial-mesenchymal transition by increasing E-cadherin and decreasing N-cadherin expression through the PI3K/Akt pathway. GSBP-2 also suppressed the angiogenesis of human umbilical vein endothelial cells. In conclusion, GSBP-2 could inhibit the proliferation, migration, and invasion of MDA-MB-231 cells and showed significant anti-angiogenic ability. These findings indicate that GSBP-2 is a promising therapeutic adjuvant for TNBC.

摘要

中国灵芝,又称灵芝,是一种具有抗肿瘤特性的药用真菌。在此,从灵芝子实体中提取的粗多糖(GSB)被用于选择性抑制三阴性乳腺癌(TNBC)细胞。GSBP-2 从 GSB 中纯化得到,分子量为 11.5 kDa,组成如下:α-l-Fucp-(1→, β-d-Glcp-(1→, β-d-GlcpA-(1→, →3)-β-d-Glcp-(1→, →3)-β-d-GlcpA-(1→, →4)-α-d-Galp-(1→,→6)-β-d-Manp-(1→, 和 →3,6)-β-d-Glcp-(1→,摩尔比为 1.0:6.3:1.7:5.5:1.5:4.3:8.0:7.9。通过噻唑蓝比色法、集落形成实验、划痕愈合实验和 Transwell 迁移实验测定 GSBP-2 对 MDA-MB-231 细胞的活性。结果表明,GSBP-2 通过调节 MDA-MB-231 细胞中上皮-间质转化(即 Snail1、ZEB1、VIM、CDH1、CDH2 和 MMP9)的靶基因,选择性抑制 MDA-MB-231 细胞的增殖、迁移和侵袭。此外,Western blot 结果表明,GSBP-2 通过增加 E-钙粘蛋白和减少 N-钙粘蛋白的表达,通过 PI3K/Akt 通路抑制上皮-间质转化。GSBP-2 还抑制了人脐静脉内皮细胞的血管生成。总之,GSBP-2 可抑制 MDA-MB-231 细胞的增殖、迁移和侵袭,表现出显著的抗血管生成能力。这些发现表明,GSBP-2 是治疗三阴性乳腺癌的一种很有前途的治疗佐剂。

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