Evidence map›Paper›PMID 21963850›Full record

ArticleOncogene2012

EGFR-dependent pancreatic carcinoma cell metastasis through Rap1 activation.

M Huang, S Anand, E A Murphy, J S Desgrosellier, D G Stupack, S J Shattil, D D Schlaepfer, D A Cheresh

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.8field-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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
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  7. Article
  8. Article
  9. Systems andFrontiers in pharmacology · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. TMEM16A controls EGF-induced calcium signaling implicated in pancreatic cancer prognosis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  20. Article
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

8 authors at 1 institution in 1 country.

M HuangDepartment of Pathology, Moores University of California San Diego Cancer Center, La Jolla, CA 92093-1503, USA.
S Anand
E A Murphy
J S Desgrosellier
D G Stupack
S J Shattil
D D Schlaepfer
D A Cheresh
University of California, San Diego · US

Funding

UCSD Cancer Center Training Program in Drug DevelopmentT32CA121938 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Michael Bouvet, Dwayne G. Stupack · 2006 to 2026
$10.3M
Discoveries at the Crossroads of Integrin and Inflammatory Signaling in PlateletsR01HL056595 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHATTIL, SANFORD J · 1996 to 2020
$7.5M
REGULATION OF TUMOR CELL ATTACHMENT BY SURFACE ANTIGENSR01CA045726 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHERESH, DAVID A · 1988 to 2017
$7.4M
Role of Focal Adhesion Kinase In TumorigenesisR01CA102310 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCHLAEPFER, DAVID D · 2003 to 2019
$5.0M
Integrins and Caspase 8 in Tumor ProgressionR01CA107263 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI STUPACK, DWAYNE G. · 2005 to 2014
$3.1M
Vascular Survival Governed by Integrin Ligation StateR01CA095262 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHERESH, DAVID A · 2002 to 2011
$2.9M
NCI NIH HHS CA045726NCI NIH HHS CA102310NCI NIH HHS CA107263NCI NIH HHS R01 CA045726NCI NIH HHS R01 CA095262NCI NIH HHS R01 CA102310NCI NIH HHS R01 CA107263NCI NIH HHS T32 CA121938NHLBI NIH HHS HL47900NHLBI NIH HHS HL56595NHLBI NIH HHS R01 HL056595
6 · The paper itself

Abstract

Tyrosine kinase receptors have an essential role in various aspects of tumor progression. In particular, epidermal growth factor receptor (EGFR) and its ligands have been implicated in the growth and dissemination of a wide array of human carcinomas. Here, we describe an EGFR-mediated signaling pathway that regulates human pancreatic carcinoma cell invasion and metastasis, yet does not influence the growth of primary tumors. In fact, ligation/activation of EGFR induces Src-dependent phosphorylation of two critical tyrosine residues of p130CAS, leading to the assembly of a Crk-associated substrate (CAS)/Nck1 complex that promotes Ras-associated protein-1 (Rap1) signaling. Importantly, GTP loading of Rap1 is specifically required for pancreatic carcinoma cell migration on vitronectin but not on collagen. Furthermore, Rap1 activation is required for EGFR-mediated metastasis in vivo without impacting primary tumor growth. These findings identify a molecular pathway that promotes the invasive/metastatic properties of human pancreatic carcinomas driven by EGFR.

Indexed as

Cell MovementAdaptor Proteins, Signal TransducingAnimalsBlotting, WesternCell ProliferationCells, CulturedChick EmbryoErbB ReceptorsHumansImmunoenzyme TechniquesImmunoprecipitationNeoplasm MetastasisOncogene ProteinsPancreatic NeoplasmsRNA, Small InterferingShelterin ComplexAdaptor Proteins, Signal TransducingEGFR protein, humanErbB ReceptorsNck proteinOncogene ProteinsRNA, Small InterferingShelterin ComplexTelomere-Binding ProteinsTERF2IP protein, human

Identifiers

PMID21963850
PMCPMC3711644
OpenAlexW2039038314

What OpenQuestion holds

Textmetadata
LicenceTDM
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.