Evidence map›Paper›PMID 31554208›Full record

ArticleCancers2019

Impact of Fibroblast-Derived SPARC on Invasiveness of Colorectal Cancer Cells.

Daniel Drev, Felix Harpain, Andrea Beer, Anton Stift, Elisabeth S Gruber, Martin Klimpfinger, Sabine Thalhammer, Andrea Reti, Lukas Kenner, Michael Bergmann and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  5. Unraveling the role of cancer-associated fibroblasts in colorectal cancer.World journal of gastrointestinal oncology · 2024
    Review
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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.

Daniel DrevDepartment of Medicine 1, Institute of Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria. daniel.drev@meduniwien.ac.at.
Felix HarpainDepartment of Surgery, Division of General Surgery, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. felix.harpain@meduniwien.ac.at.ORCID 0000-0001-6589-5712
Andrea BeerClinical Institute of Pathology, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. andrea.beer@meduniwien.ac.at.ORCID 0000-0002-0726-1233
Anton StiftDepartment of Surgery, Division of General Surgery, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. anton.stift@meduniwien.ac.at.ORCID 0000-0002-7243-8138
Elisabeth S GruberDepartment of Surgery, Division of General Surgery, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. elisabeth.s.gruber@meduniwien.ac.at.ORCID 0000-0002-8646-1865
Martin KlimpfingerDepartment of Pathology, Social Medical Center South-Kaiser Franz Josef Hospital, Kundratstraβe 3, 1100 Vienna, Austria. martin.klimpfinger@wienkav.at.
Sabine ThalhammerDepartment of Pathology, Social Medical Center South-Kaiser Franz Josef Hospital, Kundratstraβe 3, 1100 Vienna, Austria. sabine.thalhammer@wienkav.at.
Andrea RetiDepartment of Medicine 1, Institute of Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria. reti.andrea@yahoo.com.
Lukas KennerClinical Institute of Pathology, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. lukas.kenner@meduniwien.ac.at.
Michael BergmannDepartment of Surgery, Division of General Surgery, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria. michael.bergmann@meduniwien.ac.at.ORCID 0000-0001-8529-1166
Brigitte MarianDepartment of Medicine 1, Institute of Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria. brigitte.marian@meduniwien.ac.at.ORCID 0000-0001-7034-5563
Medical University of Vienna · ATKaiser-Franz-Josef-Spital · AT

Funding

Austrian Science Fund P26218Oesterreichische Nationalbank 15655
6 · The paper itself

Abstract

Secreted protein acidic and rich in cysteine (SPARC) is a matricellular protein modulating cell-matrix interactions and was found up-regulated in tumor stroma. To explore the effect of high stromal SPARC on colorectal cancer (CRC) cell behavior and clinical outcome, this study determined SPARC expression in patients suffering from stage II and III CRC using a publicly available mRNA data set and immunohistochemistry of tissue microarray sections. Moreover, in vitro co-culture models using CRC cell lines together with colon-associated fibroblasts were established to determine the effect of fibroblast-derived SPARC on cancer cells. In 466 patient samples, high SPARC mRNA was associated with a shorter disease-free survival. In 99 patients of the tissue microarray cohort, high stromal SPARC in the primary tumor was an independent predictor of shorter survival in patients with relapse (27 cases; HR = 4574,

Indexed as

3D co-culturecancer-associated fibroblastscolorectal cancerSPARCtumor microenvironment

Identifiers

PMID31554208
PMCPMC6827058
OpenAlexW2975217081

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.