Evidence map›Paper›PMID 25779666›Full record

ArticleOncotarget2015

Fatty acid binding protein 5 promotes metastatic potential of triple negative breast cancer cells through enhancing epidermal growth factor receptor stability.

Catherine A Powell, Mohd W Nasser, Helong Zhao, Jacob C Wochna, Xiaoli Zhang, Charles Shapiro, Konstantin Shilo, Ramesh K Ganju

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

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  20. The implications of signaling lipids in cancer metastasis.Experimental & molecular medicine · 2018
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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

8 authors at 2 institutions in 1 country.

Catherine A PowellDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Mohd W NasserDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Helong ZhaoDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Jacob C WochnaDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Xiaoli ZhangCenter for Biostatistics, The Ohio State University, Columbus, OH, USA.
Charles ShapiroTisch Cancer Institute, Mount Sinai School of Medicine, New York, USA.
Konstantin ShiloDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Ramesh K GanjuDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
The Ohio State University · USIcahn School of Medicine at Mount Sinai · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Role of S100A7 in breast cancer progression and metastasisR01CA153490 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2011 to 2014
$1.2M
Synthetic cannabinoids as novel therapeutic strategies against non-small cell lunR21CA163010 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2011 to 2012
$365k
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA153490NCI NIH HHS R01 CA163010NCI NIH HHS R21 CA163010
6 · The paper itself

Abstract

Fatty acid binding protein 5 (FABP5), an intracellular lipid binding protein, has been shown to play a role in various cancers, including breast cancer. However, FABP5 and its role in triple negative breast cancer (TNBC) have not been studied. We show FABP5 protein expression correlates with TNBC, high grade tumors, and worse disease-free survival in a tissue microarray containing 423 breast cancer patient samples. High FABP5 expression significantly correlates with epidermal growth factor receptor (EGFR) expression in these samples. Decreased tumor growth and lung metastasis were observed in FABP5-/- mice othotopically injected with murine breast cancer cells. FABP5 loss in TNBC tumor cells inhibited motility and invasion. Mechanistic studies revealed that FABP5 knockdown in TNBC cells results in decreased EGFR expression and FABP5 is important for EGF-induced metastatic signaling. Loss of FABP5 leads to proteasomal targeting of EGFR. Our studies show that FABP5 has a role in both host and tumor cell during breast cancer progression. These findings suggest that FABP5 mediates its enhanced effect on TNBC metastasis, in part, through EGFR, by inhibiting EGFR proteasomal degradation. These studies show, for the first time, a correlation between FABP5 and EGFR in enhancing TNBC metastasis through a novel mechanism.

Indexed as

AnimalsCell ProliferationDisease-Free SurvivalErbB ReceptorsFatty Acid-Binding ProteinsFemaleHumansMammary Neoplasms, ExperimentalMiceMice, Inbred C57BLMice, KnockoutNeoplasm MetastasisNeoplasm ProteinsSignal TransductionTriple Negative Breast NeoplasmsEGFR protein, humanEGFR protein, mouseErbB ReceptorsFABP5 protein, humanFabp5 protein, mouseFatty Acid-Binding ProteinsNeoplasm Proteinsepidermal growth factor receptorfatty acid binding protein 5metastasisprotein degradationtriple negative breast cancer

Identifiers

PMID25779666
PMCPMC4467443
OpenAlexW1840670308

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.