File Download

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

서판길

Suh, Pann-Ghill
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

A secretome profile indicative of oleate-induced proliferation of HepG2 hepatocellular carcinoma cells

Author(s)
Park, SoyeonPark, Ji-HwanJung, Hee-JungJang, Jin-HyeokAhn, SanghyunKim, YounahSuh, Pann-GhillChae, SehyunYoon, Jong HyukRyu, Sung HoHwang, Daehee
Issued Date
2018-08
DOI
10.1038/s12276-018-0120-3
URI
https://scholarworks.unist.ac.kr/handle/201301/25580
Fulltext
https://www.nature.com/articles/s12276-018-0120-3
Citation
EXPERIMENTAL AND MOLECULAR MEDICINE, v.50, pp.93
Abstract
Increased fatty acid (FA) is often observed in highly proliferative tumors. FAs have been shown to modulate the secretion of proteins from tumor cells, contributing to tumor survival. However, the secreted factors affected by FA have not been systematically explored. Here, we found that treatment of oleate, a monounsaturated omega-9 FA, promoted the proliferation of HepG2 cells. To examine the secreted factors associated with oleate-induced cell proliferation, we performed a comprehensive secretome profiling of oleate-treated and untreated HepG2 cells. A comparison of the secretomes identified 349 differentially secreted proteins (DSPs; 145 upregulated and 192 downregulated) in oleate-treated samples, compared to untreated samples. The functional enrichment and network analyses of the DSPs revealed that the 145 upregulated secreted proteins by oleate treatment were mainly associated with cell proliferation-related processes, such as lipid metabolism, inflammatory response, and ER stress. Based on the network models of the DSPs, we selected six DSPs (MIF, THBS1, PDIA3, APOA1, FASN, and EEF2) that can represent such processes related to cell proliferation. Thus, our results provided a secretome profile indicative of an oleate-induced proliferation of HepG2 cells
Publisher
NATURE PUBLISHING GROUP
ISSN
1226-3613
Keyword
ENDOPLASMIC-RETICULUM-STRESSMIGRATION INHIBITORY FACTORUNSATURATED FATTY-ACIDSBREAST-CANCER CELLSCANDIDATE SEROLOGICAL BIOMARKERSTHIOL OXIDOREDUCTASE ERP57UNFOLDED PROTEIN RESPONSEPANCREATIC-CANCERMASS-SPECTROMETRYINDUCED APOPTOSIS

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.