Abstract 1159 Modeling Physiological Lipid Availability to Improve In Vitro Studies of Lipid Metabolism

HCC1806 MCSCs and 3T3-L1 differentiated adipocytes that induce aggressive gene signatures that remodel the extracellular matrix and could promote metastasis.Further studies are in progress to validate this unique gene signature in additional AA TNBC cell lines, Caucasian American TNBC, and estrogen receptor-positive cell lines incubated with human adipocytes.We also plan to conduct knock-in and knock-out experiments in the receptor-ligand pairs to confirm the central signaling cascades involved.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1016/j.jbc.2025.108637
Primary Topic
Diet and metabolism studies
Type
article
Field-Weighted Citation Impact
0.00

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Abstract 1159 Modeling Physiological Lipid Availability to Improve In Vitro Studies of Lipid Metabolism

Vipin Rawat, Jonathan L. Coloff, Patrick B. Jonker, Kelly O. Conger et al.
Journal of Biological Chemistry
Diet and metabolism studies
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Abstract 1159 Modeling Physiological Lipid Availability to Improve In Vitro Studies of Lipid Metabolism

Vipin Rawat, Jonathan L. Coloff, Patrick B. Jonker, Kelly O. Conger, Mete Emir Özgürses, Alexander Muir, Huiping Zhao
article en

Abstract

HCC1806 MCSCs and 3T3-L1 differentiated adipocytes that induce aggressive gene signatures that remodel the extracellular matrix and could promote metastasis.Further studies are in progress to validate this unique gene signature in additional AA TNBC cell lines, Caucasian American TNBC, and estrogen receptor-positive cell lines incubated with human adipocytes.We also plan to conduct knock-in and knock-out experiments in the receptor-ligand pairs to confirm the central signaling cascades involved.

Journal of Biological ChemistryVol. 301(5)
University of Illinois Chicago (US)
National Institutes of Health
Zero hunger
Openalex Percentile: Top 82%
Diet and metabolism studies
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