Evidence map›Paper›PMID 23319743›Full record

ArticleJournal of lipid research2013

Fatty acid synthase causes drug resistance by inhibiting TNF-α and ceramide production.

Hailan Liu, Xi Wu, Zizheng Dong, Zhiyong Luo, Zhenwen Zhao, Yan Xu, Jian-Ting Zhang

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
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

43 citing papers in PubMed, 72 citations in OpenAlex.

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  14. Breast Cancer Chemoresistance: Insights into the Regulatory Role of lncRNA.International journal of molecular sciences · 2023
    Review
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  16. Novel Insights on Lipid Metabolism Alterations in Drug Resistance in Cancer.Frontiers in cell and developmental biology · 2022
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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

7 authors at 2 institutions in 1 country.

Hailan LiuDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN.
Xi WuDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN.
Zizheng DongDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN.
Zhiyong LuoDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN.
Zhenwen ZhaoDepartment of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IN.
Yan XuDepartment of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IN; IU Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.
Jian-Ting ZhangDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN; IU Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Targeting the amino terminal gate of human MRP1R01CA113384 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ZHANG, JIAN-TING · 2007 to 2011
$1.4M
NCI NIH HHS CA-113384NCI NIH HHS R01 CA113384
6 · The paper itself

Abstract

Fatty acid synthase (FASN) is a key enzyme in the synthesis of palmitate, the precursor of major nutritional, energetic, and signaling lipids. FASN expression is upregulated in many human cancers and appears to be important for cancer cell survival. Overexpression of FASN has also been found to associate with poor prognosis and higher risk of recurrence of human cancers. Indeed, elevated FASN expression has been shown to contribute to drug resistance. However, the mechanism of FASN-mediated drug resistance is currently unknown. In this study, we show that FASN overexpression causes resistance to multiple anticancer drugs via inhibiting drug-induced ceramide production, caspase 8 activation, and apoptosis. We also show that FASN overexpression suppresses tumor necrosis factor-α production and nuclear factor-κB activation as well as drug-induced activation of neutral sphingomyelinase. Thus, TNF-α may play an important role in mediating FASN function in drug resistance.

Indexed as

Antineoplastic AgentsApoptosisBlotting, WesternCell Line, TumorCeramidesDoxorubicinEnzyme-Linked Immunosorbent AssayFatty Acid SynthasesHumansNF-kappa BReverse Transcriptase Polymerase Chain ReactionTumor Necrosis Factor-alphaAntineoplastic AgentsCeramidesDoxorubicinFatty Acid SynthasesNF-kappa BTumor Necrosis Factor-alpha

Identifiers

PMID23319743
PMCPMC3617951
OpenAlexW2152675473

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.