Evidence map›Paper›PMID 19411761›Full record

ArticleThe Journal of clinical investigation2009

CEACAM6 attenuates adenovirus infection by antagonizing viral trafficking in cancer cells.

Yaohe Wang, Rathi Gangeswaran, Xingbo Zhao, Pengju Wang, James Tysome, Vipul Bhakta, Ming Yuan, C P Chikkanna-Gowda, Guozhong Jiang, Dongling Gao and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. The emerging roles of CEACAM6 in human cancer (Review).International journal of oncology · 2024
    Review
  2. Article
  3. Article
  4. Transient Inhibition of PI3Kδ Enhances the Therapeutic Effect of Intravenous Delivery of Oncolytic Vaccinia Virus.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Modification of the early gene enhancer-promoter improves the oncolytic potency of adenovirus 11.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Article
  12. Article
  13. Article
  14. Article
  15. Novel therapies for pancreatic cancer: setbacks and progress.Future oncology (London, England) · 2010
    Article
  16. 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

20 authors at 3 institutions in 2 countries.

Yaohe WangCentre for Molecular Oncology and Imaging, Institute of Cancer, Barts and The London School of Medicine and Dentistry, London, United Kingdom. yaohe.wang@cancer.org.uk
Rathi Gangeswaran
Xingbo Zhao
Pengju Wang
James Tysome
Vipul Bhakta
Ming Yuan
C P Chikkanna-Gowda
Guozhong Jiang
Dongling Gao
Fengyu Cao
Jennelle Francis
Jinxia Yu
Kangdong Liu
Hongyan Yang
Yunhan Zhang
Weidong Zang
Claude Chelala
Ziming Dong
Nick Lemoine
Queen Mary University of London · GBZhengzhou University · CNInstitute of Cancer Research · GB

Funding

Cancer Research UK C633-A6253/A6251
6 · The paper itself

Abstract

The changes in cancer cell surface molecules and intracellular signaling pathways during tumorigenesis make delivery of adenovirus-based cancer therapies inefficient. Here we have identified carcinoembryonic antigen- related cell adhesion molecule 6 (CEACAM6) as a cellular protein that restricts the ability of adenoviral vectors to infect cancer cells. We have demonstrated that CEACAM6 can antagonize the Src signaling pathway, downregulate cancer cell cytoskeleton proteins, and block adenovirus trafficking to the nucleus of human pancreatic cancer cells. Similar to CEACAM6 overexpression, treatment with a Src-selective inhibitor significantly reduced adenovirus replication in these cancer cells and normal human epithelial cells. In a mouse xenograft tumor model, siRNA-mediated knockdown of CEACAM6 also significantly enhanced the antitumor effect of an oncolytic adenovirus. We propose that CEACAM6-associated signaling pathways could be potential targets for the development of biomarkers to predict the response of patients to adenovirus-based therapies, as well as for the development of more potent adenovirus-based therapeutics.

Indexed as

AdenoviridaeAntigens, CDCell Adhesion MoleculesCell LineColorectal NeoplasmsCytoskeletonDown-RegulationGene Expression Regulation, NeoplasticGPI-Linked ProteinsHumansMicroscopy, Electron, TransmissionPancreatic NeoplasmsRNA, Small Interferingsrc-Family KinasesSubstrate SpecificityAntigens, CDCEACAM6 protein, humanCell Adhesion MoleculesGPI-Linked ProteinsRNA, Small Interferingsrc-Family Kinases

Identifiers

PMID19411761
PMCPMC2689137
OpenAlexW2110871523

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.