Evidence map›Paper›PMID 22863617›Full record

ArticleThe Journal of clinical investigation2012

Chemokine 25-induced signaling suppresses colon cancer invasion and metastasis.

Huanhuan Joyce Chen, Robert Edwards, Serena Tucci, Pengcheng Bu, Jeff Milsom, Sang Lee, Winfried Edelmann, Zeynep H Gümüs, Xiling Shen, Steven Lipkin

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Lamin A/C and the Immune System: One Intermediate Filament, Many Faces.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Chemokines and Chemokine Receptors: Orchestrating Tumor Metastasization.International journal of molecular sciences · 2018
    Review
  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

10 authors at 2 institutions in 1 country.

Huanhuan Joyce ChenDepartment of Medicine, Genetic Medicine, Weill Cornell Medical College, New York, New York, USA.
Robert Edwards
Serena Tucci
Pengcheng Bu
Jeff Milsom
Sang Lee
Winfried Edelmann
Zeynep H Gümüs
Xiling Shen
Steven Lipkin
Cornell University · USUniversity of California, Irvine · US

Funding

DNA Mismatch Repair and associated genes in suppression of GI adenomas and carcinR01CA098626 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LIPKIN, STEVEN M · 2004 to 2014
$2.9M
Multi-scale modeling of asymmetric cell divisionR01GM095990 · NIGMS · CORNELL UNIVERSITY · PI SHEN, XILING · 2011 to 2015
$1.5M
NCI NIH HHS R01 CA098626NCI NIH HHS R21 CA122937NIGMS NIH HHS R01 GM095990
6 · The paper itself

Abstract

Chemotactic cytokines (chemokines) can help regulate tumor cell invasion and metastasis. Here, we show that chemokine 25 (CCL25) and its cognate receptor chemokine receptor 9 (CCR9) inhibit colorectal cancer (CRC) invasion and metastasis. We found that CCR9 protein expression levels were highest in colon adenomas and progressively decreased in invasive and metastatic CRCs. CCR9 was expressed in both primary tumor cell cultures and colon-cancer-initiating cell (CCIC) lines derived from early-stage CRCs but not from metastatic CRC. CCL25 stimulated cell proliferation by activating AKT signaling. In vivo, systemically injected CCR9+ early-stage CCICs led to the formation of orthotopic gastrointestinal xenograft tumors. Blocking CCR9 signaling inhibited CRC tumor formation in the native gastrointestinal CCL25+ microenvironment, while increasing extraintestinal tumor incidence. NOTCH signaling, which promotes CRC metastasis, increased extraintestinal tumor frequency by stimulating CCR9 proteasomal degradation. Overall, these data indicate that CCL25 and CCR9 regulate CRC progression and invasion and further demonstrate an appropriate in vivo experimental system to study CRC progression in the native colon microenvironment.

Indexed as

Signal TransductionAdenocarcinomaAnimalsBasic Helix-Loop-Helix ProteinsCell Line, TumorChemokines, CCChemotaxisColorectal NeoplasmsGene Expression Regulation, NeoplasticGene Regulatory NetworksHomeodomain ProteinsMiceMice, Inbred NODMice, SCIDNeoplasm InvasivenessNeoplasm TransplantationBasic Helix-Loop-Helix ProteinsCC chemokine receptor 9CCL25 protein, humanChemokines, CCHES1 protein, humanHomeodomain ProteinsReceptors, CCRTranscription Factor HES-1

Identifiers

PMID22863617
PMCPMC3428084
OpenAlexW2039068432

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.