Expression of Globo H and SSEA3 in breast cancer, stem cells and the involvement of fucosyl transferases 1 and 2 in Globo H synthesis

被引:133
作者
Chang, Wen-Wei [1 ]
Lee, Chien Hsin [1 ]
Lee, Peishan [1 ]
Lin, Juway [1 ,3 ]
Hsu, Chun-Wei [1 ]
Hung, Jung-Tung [1 ]
Lin, Jin-Jin [1 ]
Yu, Jyh-Cherng [4 ]
Shao, Li-en [1 ]
Yu, John [1 ,2 ]
Wong, Chi-Huey [1 ]
Yu, Alice L. [1 ]
机构
[1] Acad Sinica, Genom Res Ctr, Taipei 115, Taiwan
[2] Acad Sinica, Inst Cellular & Organism Biol, Taipei 115, Taiwan
[3] Natl Taiwan Univ, Inst Biochem Sci, Taipei 106, Taiwan
[4] Tri Serv Gen Hosp, Dept Surg, Taipei 114, Taiwan
关键词
D O I
10.1073/pnas.0804979105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We examined the expression in breast cancer stem cells (BCSCs) of Globo H, a potential tumor-associated antigen for immunotherapy of epithelial cancers including breast cancer. Flow cytometry revealed Globo H expression in 25/41 breast cancer specimens (61.0%). Non-BCSCs from 25/25 and BCSCs from 8/40 (20%) expressed Globo H. We showed the expression of stage-specific embryonic antigen 3 (SSEA3), the pentasaccharide precursor of Globo H, in 31/40 (77.5%) tumors. Non- BCSCs from 29/31 and BCSCs from 25/40 (62.5%) expressed SSEA3. Like Globo H, SSEA3 expression in normal tissues was predominately at the secretory borders of epithelium, where access to the immune system is restricted. Immunization of mice with Globo H-KLH and alpha-GalCer induced antibodies reactive with Globo H and SSEA3, suggesting that a Globo H-based vaccine will target tumor cells expressing Globo H or SSEA3. We next sought to reduce Globo H expression by siRNA targeting fucosyltransferase (FUT) 1 and 2, which mediate alpha-1,2 linkage of fucose to SSEA3 to generate Globo H. We showed both genes to be involved in the biosynthesis of Globo H. Moreover, FUT2 expression in BCSCs was significantly lower than in non-BCSCs harvested from a primary human breast cancer in NOD/SCID mouse, whereas FUT1 was slightly lower in BCSCs. Thus, the lower expression of Globo H in BCSCs may be attributed to less FUT2/FUT1, and to reduced SSEA3 in BCSCs compared with non-BCSCs. Our findings provide insight into further development of a Globo H-based vaccine and FUT1/FUT2-targeted therapy for breast cancer.
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收藏
页码:11667 / 11672
页数:6
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