Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.bbrc.2018.04.075
Title: Sphingolipidomics analysis of large clinical cohorts. Part 2: Potential impact and applications
Authors: Chong, Joyce R 
Xiang, Ping 
Wang, Wei 
Hind, Tatsuma
Chew, Wee Siong 
Ong, Wei-Yi 
Lai, Mitchell KP 
Herr, Deron R 
Keywords: Science & Technology
Life Sciences & Biomedicine
Biochemistry & Molecular Biology
Biophysics
Sphingolipid
Lipidomics
Dementia
Stroke
Cancer
Autoimmune disease
Sphingomyelin
Ceramide
Sphingomyelinase
Sphingosine-l-phosphate
Neutral sphingomyelinase 2 (nSMase2)
SPHINGOSINE 1-PHOSPHATE RECEPTOR-2
ALZHEIMERS-DISEASE
CERAMIDE LEVELS
INTRACEREBRAL HEMORRHAGE
WHITE-MATTER
CELL-DEATH
CANCER
SPHINGOSINE-1-PHOSPHATE
FINGOLIMOD
PLASMA
Issue Date: 7-Oct-2018
Publisher: ACADEMIC PRESS INC ELSEVIER SCIENCE
Citation: Chong, Joyce R, Xiang, Ping, Wang, Wei, Hind, Tatsuma, Chew, Wee Siong, Ong, Wei-Yi, Lai, Mitchell KP, Herr, Deron R (2018-10-07). Sphingolipidomics analysis of large clinical cohorts. Part 2: Potential impact and applications. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 504 (3) : 602-607. ScholarBank@NUS Repository. https://doi.org/10.1016/j.bbrc.2018.04.075
Abstract: It has been known for decades that the regulation of sphingolipids (SLs) is essential for the proper function of many cellular processes. However, a complete understanding of these processes has been complicated by the structural diversity of these lipids. A well-characterized metabolic pathway is responsible for homeostatic maintenance of hundreds of distinct SL species. This pathway is perturbed in a number of pathological processes, resulting in derangement of the “sphingolipidome.” Recently, advances in mass spectrometry (MS) techniques have made it possible to characterize the sphingolipidome in large-scale clinical studies, allowing for the identification of specific SL molecules that mediate pathological processes and/or may serve as biomarkers. This manuscript provides an overview of the functions of SLs, and reviews previous studies that have used MS techniques to identify changes to the sphingolipidome in non-metabolic diseases.
Source Title: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
URI: https://scholarbank.nus.edu.sg/handle/10635/188523
ISSN: 0006291X
10902104
DOI: 10.1016/j.bbrc.2018.04.075
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