Genomics Research Center, Academia Sinica, Taipei, 11529, Taiwan.
Institute of Basic Medical Science, National Cheng Kung University, Tainan, 70101, Taiwan.
Proc Natl Acad Sci U S A. 2019 Feb 26;116(9):3518-3523. doi: 10.1073/pnas.1816946116. Epub 2019 Feb 11.
The globo-series glycosphingolipids (GSLs) SSEA3, SSEA4, and Globo-H specifically expressed on cancer cells are found to correlate with tumor progression and metastasis, but the functional roles of these GSLs and the key enzyme β1,3-galactosyltransferase V (β3GalT5) that converts Gb4 to SSEA3 remain largely unclear. Here we show that the expression of β3GalT5 significantly correlates with tumor progression and poor survival in patients, and the globo-series GSLs in breast cancer cells form a complex in membrane lipid raft with caveolin-1 (CAV1) and focal adhesion kinase (FAK) which then interact with AKT and receptor-interacting protein kinase (RIP), respectively. Knockdown of β3GalT5 disrupts the complex and induces apoptosis through dissociation of RIP from the complex to interact with the Fas death domain (FADD) and trigger the Fas-dependent pathway. This finding provides a link between SSEA3/SSEA4/Globo-H and the FAK/CAV1/AKT/RIP complex in tumor progression and apoptosis and suggests a direction for the treatment of breast cancer, as demonstrated by the combined use of antibodies against Globo-H and SSEA4.
糖脂(GSL)globo 系列 SSEA3、SSEA4 和 Globo-H 特异性表达于癌细胞,与肿瘤进展和转移相关,但这些 GSL 以及将 Gb4 转化为 SSEA3 的关键酶β1,3-半乳糖基转移酶 V(β3GalT5)的功能作用在很大程度上仍不清楚。本研究显示,β3GalT5 的表达与患者的肿瘤进展和不良预后显著相关,乳腺癌细胞中的糖脂 globo 系列与质膜筏中的小窝蛋白-1(CAV1)和粘着斑激酶(FAK)形成复合物,然后分别与 AKT 和受体相互作用蛋白激酶(RIP)相互作用。β3GalT5 的敲低会破坏复合物,通过将 RIP 从复合物中解离出来与 Fas 死亡结构域(FADD)相互作用并触发 Fas 依赖性途径,从而诱导细胞凋亡。这一发现为 SSEA3/SSEA4/Globo-H 与肿瘤进展和凋亡过程中的 FAK/CAV1/AKT/RIP 复合物之间提供了联系,并提示了一种治疗乳腺癌的方向,如通过联合使用抗 Globo-H 和 SSEA4 的抗体所证明的那样。