Evidence map›Paper›PMID 30670778›Full record

ArticleOncogene2019

ATF3 and JDP2 deficiency in cancer associated fibroblasts promotes tumor growth via SDF-1 transcription.

Shimrit Avraham, Ben Korin, Sharon Aviram, Dvir Shechter, Yuval Shaked, Ami Aronheim

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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  14. Induction of heparanase 2 (Hpa2) expression by stress is mediated by ATF3.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  15. Article
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  17. Prevention of tumor risk associated with the reprogramming of human pluripotent stem cells.Journal of experimental & clinical cancer research : CR · 2020
    Review
  18. Article
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  20. Review
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

6 authors at 1 institution in 1 country.

Shimrit AvrahamDepartment of Cell Biology and Cancer Science, The B. Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Ben KorinDepartment of Immunology, Department of Neuroscience, The B. Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Sharon AviramDepartment of Cell Biology and Cancer Science, The B. Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Dvir ShechterDepartment of Cell Biology and Cancer Science, The B. Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Yuval ShakedDepartment of Cell Biology and Cancer Science, The B. Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel. yshaked@technion.ac.il.
Ami AronheimDepartment of Cell Biology and Cancer Science, The B. Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel. aronheim@technion.ac.il.
Technion – Israel Institute of Technology · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activating transcription factor 3 (ATF3) and the c-Jun dimerization protein 2 (JDP2) are members of the basic leucine zipper (bZIP) family of transcription factors. These proteins share a high degree of homology and both can activate or repress transcription. Deficiency of either one of them in the non-cancer host cells was shown to reduce metastases. As ATF3 and JDP2 compensate each other's function, we studied the double deficiency of ATF3 and JDP2 in the stromal tumor microenvironment. Here, we show that mice with ATF3 and JDP2 double deficiency (designated thereafter dKO) developed larger tumors with high vascular perfusion and increased cell proliferation rate compared to wild type (WT) mice. We further identify that the underlying mechanism involves tumor associated fibroblasts which secrete high levels of stromal cell-derived factor 1 (SDF-1) in dKO fibroblasts. SDF-1 depletion in dKO fibroblasts dampened tumor growth and blood vessel perfusion. Furthermore, ATF3 and JDP2 were found to regulate SDF-1 transcription and secretion in fibroblasts, a phenomenon that is potentiated in the presence of cancer cells. Collectively, our results suggest that ATF3 and JDP2 regulate the expression of essential tumor promoting factors expressed by fibroblasts within the tumor microenvironment, and thus restrain tumor growth.

Indexed as

Activating Transcription Factor 3AnimalsBlood VesselsBone Marrow TransplantationCancer-Associated FibroblastsCell ProliferationChemokine CXCL12FemaleGene Expression Regulation, NeoplasticHEK293 CellsHumansMice, Inbred C57BLMice, KnockoutNeoplasms, ExperimentalRepressor ProteinsTumor MicroenvironmentActivating Transcription Factor 3Atf3 protein, mouseChemokine CXCL12Cxcl12 protein, mouseJDP2 protein, humanRepressor Proteins

Identifiers

PMID30670778
PMCPMC6756089
OpenAlexW2913062036

What OpenQuestion holds

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LicenceCC BY
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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.