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