Evidence map›Paper›PMID 31294477›Full record

ArticleThe EMBO journal2019

The tumor cell-secreted matricellular protein WISP1 drives pro-metastatic collagen linearization.

Hong Jia, Jagadeesh Janjanam, Sharon C Wu, Ruishan Wang, Glendin Pano, Marina Celestine, Ophelie Martinot, Hannah Breeze-Jones, Georgia Clayton, Cecile Garcin and 4 more

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

38 citing papers in PubMed, 48 citations in OpenAlex.

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  17. An overview of CCN4 (WISP1) role in human diseases.Journal of translational medicine · 2024
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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

14 authors at 2 institutions in 1 country.

Hong JiaDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Jagadeesh JanjanamDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Sharon C WuDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Ruishan WangDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Glendin PanoDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Marina CelestineDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Ophelie MartinotDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Hannah Breeze-JonesDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Georgia ClaytonDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Cecile GarcinDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Abbas ShirinifardDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.
Ana Maria ZaskeDivision of Cardiology, Department of Internal Medicine, UTHealth - The University of Texas Health Science Center at Houston, Houston, TX, USA.
David FinkelsteinDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Myriam LabelleDepartment of Developmental Neurobiology, Comprehensive Cancer Center, Solid Tumor Program, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-3451-1186
St. Jude Children's Research Hospital · USThe University of Texas Health Science Center at Houston · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
American Lebanese Syrian Associated Charities (ALSAC)HHS|NIH|National Cancer Institute (NCI) NCI P30 CA021765NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

Collagen linearization is a hallmark of aggressive tumors and a key pathogenic event that promotes cancer cell invasion and metastasis. Cell-generated mechanical tension has been proposed to contribute to collagen linearization in tumors, but it is unknown whether other mechanisms play prominent roles in this process. Here, we show that the secretome of cancer cells is by itself able to induce collagen linearization independently of cell-generated mechanical forces. Among the tumor cell-secreted factors, we find a key role in this process for the matricellular protein WISP1 (CCN4). Specifically, WISP1 directly binds to type I collagen to promote its linearization in vitro (in the absence of cells) and in vivo in tumors. Consequently, WISP1-induced type I collagen linearization facilitates tumor cell invasion and promotes spontaneous breast cancer metastasis, without significantly affecting gene expression. Furthermore, higher WISP1 expression in tumors from cancer patients correlates with faster progression to metastatic disease and poor prognosis. Altogether, these findings reveal a conceptually novel mechanism whereby pro-metastatic collagen linearization critically depends on a cancer cell-secreted factor.

Indexed as

AnimalsBreast NeoplasmsCCN Intercellular Signaling ProteinsCell Line, TumorCell ProliferationCollagen Type IDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMiceNeoplasm MetastasisNeoplasm TransplantationPrognosisProto-Oncogene ProteinsTransforming Growth Factor beta1CCN4 protein, humanCCN Intercellular Signaling ProteinsCollagen Type IProto-Oncogene ProteinsTGFB1 protein, humanTransforming Growth Factor beta1breast cancercollageninvasionmetastasisWISP1

Identifiers

PMID31294477
PMCPMC6694215
OpenAlexW2961700625

What OpenQuestion holds

Textmetadata
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.