Evidence map›Paper›PMID 30442117›Full record

ArticleBMC cancer2018

Fatty acid binding protein 7 may be a marker and therapeutic targets in clear cell renal cell carcinoma.

Kazuhiro Nagao, Nachi Shinohara, Frank Smit, Mirjam de Weijert, Sander Jannink, Yuji Owada, Peter Mulders, Egbert Oosterwijk, Hideyasu Matsuyama

Abstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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

9 authors.

Kazuhiro NagaoDepartment of Urology, Graduate School of Medicine, Yamaguchi University, 1-1-1, Minami-Kogushi, Ube, Yamaguchi, 755-8505, Japan. knag4112@yamaguchi-u.ac.jp.
Nachi ShinoharaDepartment of Urology, Graduate School of Medicine, Yamaguchi University, 1-1-1, Minami-Kogushi, Ube, Yamaguchi, 755-8505, Japan.
Frank SmitDepartment of Urology, Radboud University Medical Center, Nijmegen 267 Experimental Urology, Geert Grooteplein, 26-28, P.O. Box 9101, NL-6525, GA, Nijmegen, The Netherlands.
Mirjam de WeijertDepartment of Urology, Radboud University Medical Center, Nijmegen 267 Experimental Urology, Geert Grooteplein, 26-28, P.O. Box 9101, NL-6525, GA, Nijmegen, The Netherlands.
Sander JanninkDepartment of Urology, Radboud University Medical Center, Nijmegen 267 Experimental Urology, Geert Grooteplein, 26-28, P.O. Box 9101, NL-6525, GA, Nijmegen, The Netherlands.
Yuji OwadaDepartment of Organ Anatomy, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan.
Peter MuldersDepartment of Urology, Radboud University Medical Center, Nijmegen 267 Experimental Urology, Geert Grooteplein, 26-28, P.O. Box 9101, NL-6525, GA, Nijmegen, The Netherlands.
Egbert OosterwijkDepartment of Urology, Radboud University Medical Center, Nijmegen 267 Experimental Urology, Geert Grooteplein, 26-28, P.O. Box 9101, NL-6525, GA, Nijmegen, The Netherlands.
Hideyasu MatsuyamaDepartment of Urology, Graduate School of Medicine, Yamaguchi University, 1-1-1, Minami-Kogushi, Ube, Yamaguchi, 755-8505, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo identify potential therapeutic target in clear cell renal cell carcinoma (ccRCC), we performed a transcriptome analysis. Our analysis showed that fatty acid binding protein 7 (FABP7) has the highest mean differential overexpression in ccRCC compared to normal kidney. We aimed to investigate the significance of FABP7 in ccRCC.

methodsImmunohistochemical staining for 40 advanced ccRCC cases was performed to investigate correlation between clinicopathological parameters and FABP7. They were composed of 40-83 years old cases with 33 male, 22 cases with pT ≥ 3, 19 cases with M1, and 16 cases with grade 3. The effect of gene knockdown was analysed by a cell viability assay and invasion assay in FABP7-overexpressing cell lines (SKRC7 and SKRC10).

resultsOur immunohistochemical analysis showed that higher FABP7 expression significantly correlated with distant metastasis and poor cancer-specific survival (CSS; both p < 0.05). Functional suppression of FABP7 significantly inhibited SKRC10 cell growth (p < 0.05) and resulted in a significant reduction of the invasive potential (p < 0.01), but did not cause growth inhibition of SKRC7 cells. We found that The Cancer Genome Atlas Research Network (TCGA) database shows FABP6 and 7 as equally overexpressed in the FABP family. Functional suppression of fatty acid binding protein 6 (FABP6) resulted in significant growth inhibition of SKRC7 cells (p < 0.005).

conclusionsFunctional suppression of FABP7 significantly reduced cell viability and invasive potential in a ccRCC cell line. FABP7 may play a role in progression in some metastatic ccRCCs. The suppressed function may be compensated by another FABP family member.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsBiomarkers, TumorCarcinoma, Renal CellCell Line, TumorCell SurvivalDisease ProgressionFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsFemaleGastrointestinal HormonesGene Expression ProfilingGene Expression Regulation, NeoplasticGene Knockdown TechniquesAntineoplastic AgentsBiomarkers, TumorFABP7 protein, humanfatty acid-binding protein 6Fatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsGastrointestinal HormonesRNA, Small InterferingTumor Suppressor ProteinsClear cell renal cell carcinomaFatty acid binding protein 6Fatty acid binding protein 7Prognostic markerTherapeutic target

Identifiers

PMID30442117
PMCPMC6238291

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Registered trials

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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.