Evidence map›Paper›PMID 29340091›Full record

ArticleOncotarget2017

Fatty acid binding protein 4 enhances prostate cancer progression by upregulating matrix metalloproteinases and stromal cell cytokine production.

Mingguo Huang, Shintaro Narita, Takamitsu Inoue, Atsushi Koizumi, Mitsuru Saito, Hiroshi Tsuruta, Kazuyuki Numakura, Shigeru Satoh, Hiroshi Nanjo, Takehiko Sasaki and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Mingguo HuangDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Shintaro NaritaDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Takamitsu InoueDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Atsushi KoizumiDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Mitsuru SaitoDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Hiroshi TsurutaDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Kazuyuki NumakuraDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Shigeru SatohDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Hiroshi NanjoDepartment of Clinical Pathology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Takehiko SasakiResearch Center for Biosignal, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Tomonori HabuchiDepartment of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Akita University · JPJapan Agency for Medical Research and Development · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fatty acid binding protein 4 (FABP4) is an abundant protein in adipocytes, and its production is influenced by high-fat diet (HFD) or obesity. The prostate stromal microenvironment induces proinflammatory cytokine production, which is key for the development and progression of prostate cancer (PCa). Here, we show that high FABP4 expression and its secretion by PCa cells directly stimulated PCa cell invasiveness by upregulating matrix metalloproteinases through phosphatidylinositol 3-kinase and mitogen-activated protein kinase signaling pathways. In addition, prostate stromal cells augmented PCa cell invasiveness by secreting interleukin-8 and -6 in response to FABP4. This was abrogated by the FABP4 specific inhibitor, BMS309403. Furthermore, a mouse xenograft experiment showed HFD enhanced PCa metastasis and invasiveness by the upregulation of FABP4 and interleukin-8. Clinically, the serum level of FABP4 was significantly associated with an aggressive type of PCa rather than obesity. Taken together, FABP4 may enhance PCa progression and invasiveness by upregulating matrix metalloproteinases and cytokine production in the PCa stromal microenvironment, especially under HFD or obesity.

Indexed as

cancer microenvironmentfatty acid binding protein 4high-fat dietprostate cancerprostate stromal cell

Identifiers

PMID29340091
PMCPMC5762359
OpenAlexW2772560157

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.