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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 |
Appears in Collections: | Staff Publications Elements |
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