Evidence map›Paper›PMID 24626200›Full record

ArticleCell cycle (Georgetown, Tex.)2014

CRABP1 provides high malignancy of transformed mesenchymal cells and contributes to the pathogenesis of mesenchymal and neuroendocrine tumors.

Yaroslav Kainov, Irina Favorskaya, Vera Delektorskaya, Galina Chemeris, Andrei Komelkov, Anna Zhuravskaya, Lyubov Trukhanova, Elina Zueva, Bertrand Tavitian, Natalya Dyakova and 2 more

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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  13. The microRNA signatures: aberrantly expressed miRNAs in prostate cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Review
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  20. Expression and clinical significance of CRABP1 and CRABP2 in non-small cell lung cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
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

12 authors.

Yaroslav KainovN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Irina FavorskayaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Vera DelektorskayaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Galina ChemerisN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Andrei KomelkovN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Anna ZhuravskayaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Lyubov TrukhanovaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Elina ZuevaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Bertrand TavitianN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Natalya DyakovaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Irina ZborovskayaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.
Elena TchevkinaN.N. Blokhin Russian Cancer Research Center; Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CRABP1 (cellular retinoic acid binding protein 1) belongs to the family of fatty acid binding proteins. Retinoic acid binding is the only known functional activity of this protein. The role of CRABP1 in human carcinogenesis remains poorly understood. Here, for the first time we demonstrated pro-metastatic and pro-tumorigenic activity of CRABP1 in mesenchymal tumors. Further functional analysis revealed that the pro-tumorigenic effect of CRABP1 does not depend on retinoic acid binding activity. These results suggest that CRABP1 could have an alternative intracellular functional activity that contributes to the high malignancy of transformed mesenchymal cells. Microarray analysis detected CRABP1-mediated alterations in the expression of about 100 genes, including those encoding key regulatory proteins. CRABP1 is ubiquitously expressed in monophasic synovial sarcomas, while in biphasic synovial sarcomas it is expressed uniquely by the spindle cells of the aggressive mesenchymal component. High level of CRABP1 expression is associated with lymph node metastasis and poor differentiation/high grade of pancreatic neuroendocrine tumors (pNETs). Presented data suggest CRABP1 as a promising biomarker of pNETs' clinical behavior. Our results give the first evidence of pro-tumorigenic and pro-metastatic activity of CRABP1 in mesenchymal and neuroendocrine tumors.

Indexed as

AdultAgedCell Line, TransformedFemaleFibroblastsHumansMaleMesenchymal Stem CellsMiddle AgedNeoplasm MetastasisNeuroendocrine TumorsPancreatic NeoplasmsReceptors, Retinoic AcidSarcoma, SynovialTretinoinReceptors, Retinoic Acidretinoic acid binding protein I, cellularTretinoinCRABP1metastasispancreatic neuroendocrine tumorssynovial sarcomastumorigenicity

Identifiers

PMID24626200
PMCPMC4050158

What OpenQuestion holds

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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.