Gangliosides profiling in serum of breast cancer patient: GM3 as a potential diagnostic biomarker

被引:0
|
作者
Qinying Li
Mei Sun
Mingsheng Yu
Qianyun Fu
Hao Jiang
Guangli Yu
Guoyun Li
机构
[1] Ocean University of China,Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Shandong Provincial Key Laboratory of Glycoscience and Glycotechnology
[2] Qingdao University Medical College,Qingdao Municipal Hospital, The Affiliated Qingdao Municipal Hospital
[3] Qingdao National Laboratory for Marine Science and Technology,Laboratory for Marine Drugs and Bioproducts
来源
Glycoconjugate Journal | 2019年 / 36卷
关键词
Breast cancer; Biomarker; Gangliosides; GM3; Serum;
D O I
暂无
中图分类号
学科分类号
摘要
Gangliosides altered during the pathological conditions and particularly in cancers. Here, we aimed to profile the gangliosides in breast cancer serum and propose potential biomarkers. LC-FTMS method was first used to identify all the ganglioside species in serum, then LC-MS/MS-MRM method was employed to quantitate the levels of gangliosides in serum from healthy volunteers and patients with benign breast tumor or breast cancer. 49 ganglioside species were determined, including GM1, GM2, GM3, GD1, GD3 and GT1 species. Compared to healthy volunteers, the levels of GM1, GM2, GM3, GD1 and GD3 displayed a rising trend in breast cancer patients. In particular, as the major glycosphingolipid component, GM3 showed excellent diagnostic accuracy in cancer serum (AUC > 0.9). PCA profile of the GM3 species showed clear distinction between normal and cancer serum. What’s more, ROC curve proved great diagnostic accuracy of GM3 between cancer and benign serum. In addition, GM3 was discovered as a diagnostic marker to differentiate luminal B subtype from other subtypes. Furthermore, a positive correlation between GM3 and Ki-67 status of patients was identified. In conclusion, our results introduced the alteration patterns of serum gangliosides in breast cancer and suggested serum GM3 as a potential diagnostic biomarker in breast cancer diagnosis and luminal B subtype distinction.
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页码:419 / 428
页数:9
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