Evidence map›Paper›PMID 42579480›Full record

ArticleDiabetes2026

Substrate-Selective Lipolysis Facilitates Unsaturated TAG Accumulation in Obesity.

Jianting Sheng, Shaohua Qi, Michael Chan, Elaine Wang, Xianlin Han, Willa A Hsueh, Li Yang, Stephen T C Wong

Abstract read
In one paragraph

Article in Diabetes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jianting ShengSystems Medicine and Bioengineering Department, Houston Methodist Neal Cancer Center, Houston Methodist Hospital, Houston, TX.
Shaohua QiSystems Medicine and Bioengineering Department, Houston Methodist Neal Cancer Center, Houston Methodist Hospital, Houston, TX.
Michael ChanSystems Medicine and Bioengineering Department, Houston Methodist Neal Cancer Center, Houston Methodist Hospital, Houston, TX.
Elaine WangSystems Medicine and Bioengineering Department, Houston Methodist Neal Cancer Center, Houston Methodist Hospital, Houston, TX.
Xianlin HanBarshop Institute for Longevity and Aging Studies and Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Willa A HsuehDiabetes and Metabolism Research Center, Division of Endocrinology, Diabetes & Metabolism, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, OH.
Li YangSystems Medicine and Bioengineering Department, Houston Methodist Neal Cancer Center, Houston Methodist Hospital, Houston, TX.ORCID 0000-0003-1421-7377
Stephen T C WongSystems Medicine and Bioengineering Department, Houston Methodist Neal Cancer Center, Houston Methodist Hospital, Houston, TX.ORCID 0000-0001-9188-6502

Funding

Systematic modeling and prediction of cell-type-specific and spatiotemporal crosstalk pathways in Alzheimer's DiseaseR01AG071496 · NIA · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KIM, DOO YEON, WONG, STEPHEN TC · 2021 to 2025
$4.0M
Systematic Alzheimer's disease drug repositioning (SMART) based on bioinformatics-guided phenotype screening and image-omicsR01AG057635 · NIA · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2018 to 2022
$3.5M
Spatiotemporal modeling of cancer-niche interactions in breast cancer bone metastasisU01CA253553 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC, ZHANG, XIANG · 2020 to 2024
$3.0M
Systematic identification of astrocyte-tumor crosstalk regulating brain metastatic tumorsR01CA238727 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC, ZHAO, HONG · 2020 to 2024
$2.6M
NCI NIH HHS R01 CA238727NCI NIH HHS R01CA238727NCI NIH HHS U01 CA253553NCI NIH HHS U01CA253553NIA NIH HHS R01 AG057635NIA NIH HHS R01AG057635NIA NIH HHS R01 AG071496NIA NIH HHS R01AG071496W.F. Chao Foundation
6 · The paper itself

Abstract

Obese adipose tissue is enriched in unsaturated triacylglycerol (TAG) species, yet the mechanisms driving this lipid remodeling remain incompletely understood. In this study, we conducted comprehensive lipidomic profiling of white adipose tissue from predominantly midlife obese individuals and consistently observed an enrichment of unsaturated TAG species. Acyl chain analysis of both TAGs and glycerophospholipids revealed a predominance of  C18 unsaturated fatty acids (FAs), particularly FA 18:1 and FA 18:2. To investigate the mechanistic basis of this selective enrichment, we performed integrated functional assays of lipogenesis and lipolysis in adipocytes under substrate-rich conditions. We found that adipose triglyceride lipase (ATGL), the rate-limiting enzyme in TAG hydrolysis, exhibits substrate selectivity: preferentially hydrolyzing saturated TAGs while displaying reduced activity toward unsaturated TAGs. This substrate-selective lipolysis impairs the mobilization of unsaturated TAGs, leading to their preferential retention and accumulation in obese adipose tissue. These findings reveal a previously underappreciated mechanism of lipid remodeling in obesity, whereby ATGL-mediated substrate specificity contributes to the disproportionate accumulation of unsaturated TAGs. This molecular insight highlights the importance of lipase selectivity in shaping adipose lipid composition and maintaining metabolic homeostasis. ARTICLE HIGHLIGHTS: Obesity is associated with the enrichment of unsaturated triacylglycerol (TAG) species in adipose tissue, but the mechanism driving this selective lipid accumulation remains unclear. We investigated whether substrate-selective lipolysis contributes to the retention of unsaturated fatty acids (FAs) in obese adipose tissue. Lipidomic profiling revealed predominant enrichment of FA 18:1 and FA 18:2 in midlife-predominant obese adipose TAGs, and functional assays showed that adipose triglyceride lipase preferentially hydrolyzes saturated TAGs under conditions of sufficient substrate supply. These results identify lipase substrate selectivity as a mechanistic contributor to lipid remodeling in obesity and a potential target for modulating adipose lipid turnover.

Indexed as

Adipose Tissue, WhiteFatty Acids, UnsaturatedLipolysisObesityTriglyceridesAcyltransferasesAdipocytesAnimalsHumansLipaseLipidomicsLipogenesisSubstrate SpecificityAcyltransferasesFatty Acids, UnsaturatedLipaseTriglycerides

Identifiers

PMID42579480
PMCPMC13593588

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.