Evidence map›Paper›PMID 23659962›Full record

ArticleMolecular oncology2013

Enrichment map profiling of the cancer invasion front suggests regulation of colorectal cancer progression by the bone morphogenetic protein antagonist, gremlin-1.

George S Karagiannis, Aaron Berk, Apostolos Dimitromanolakis, Eleftherios P Diamandis

Open access · bronzeAbstract read
In one paragraph

Article in Molecular oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
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  8. Regulation of Molecular Targets in Osteosarcoma Treatment.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Cancer-associated fibroblasts in colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Photothermal modulation of human stem cells using light-responsive 2D nanomaterials.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Article
  17. 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

4 authors at 2 institutions in 1 country.

George S KaragiannisDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Aaron Berk
Apostolos Dimitromanolakis
Eleftherios P Diamandis
Mount Sinai Hospital · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cancer invasion front (CIF), a spatially-recognized area due to the frequent presence of peritumoral desmoplastic reaction, represents a cancer site where many hallmarks of cancer metastasis occur. It is now strongly suggested that the desmoplastic microenvironment holds crucial information for determining tumor development and progression. Despite extensive research on tumor-host cell interactions at CIFs, the exact paracrine molecular network that is hardwired into the proteome of the stromal and cancer subpopulations remains partially understood. Here, we interrogated the signaling pathways and the molecular functional signatures across the proteome of a desmoplastic coculture model system of colorectal cancer progression. We discovered a group of bone morphogenetic protein (BMP) antagonists that coordinates major biological programs in CIFs, including cell proliferation, invasion, migration and differentiation processes. Using a mathematical model of cancer cell progression, coupled to in vitro cell migration assays, we demonstrated that the prominent BMP antagonist gremlin-1 (GREM1) may trigger motility of cancer cell cohorts. Our data collectively demonstrate that the desmoplastic CIFs deploy a microenvironmental signature, based on BMP antagonism, in order to regulate the motogenic fates of cancer cell cohorts invading the adjacent stroma.

Indexed as

Cell Line, TumorCell MovementColorectal NeoplasmsComputational BiologyHumansIntercellular Signaling Peptides and ProteinsModels, MolecularGREM1 protein, humanIntercellular Signaling Peptides and Proteinsalpha-smooth muscle actinAmerican type culture collectionATCCBMP(I)Bone morphogenetic proteinbone morphogenetic protein (inhibitor)CAFcancer-associated fibroblastCancer-associated fibroblastscancer invasion frontCIFCOL12A1collagen type XIIcolorectal cancerColorectal cancerCRCDesmoplasiadesmoplastic protein datasetDMEMDPDDulbecco's modified Eagle's mediumECMEMTepithelial-to-mesenchymal transitionextracellular matrixFBSfetal bovine serumfollistatinfollistatin-like 3FSTFSTL3gene ontologyGOGREM1gremlin-1Gremlin-1hepatocyte growth factorHGFhigh temperature requirement A3HTRA3ingenuity pathway analysisingenuity pathway knowledgebaseIPAIPKBLOXlysine-6-oxidaseMigrationPDGFplatelet-derived growth factorTGF-βtransforming growth factor-betauPAurokinase-type plasminogen activatorvascular endothelial growth factor (receptor-2)VEGF(R2)α-SMA

Identifiers

PMID23659962
PMCPMC5528431
OpenAlexW2153243072

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.