Evidence map›Paper›PMID 31797958›Full record

ArticleScientific reports2019

Carcinoembryonic antigen cell adhesion molecule 6 (CEACAM6) in Pancreatic Ductal Adenocarcinoma (PDA): An integrative analysis of a novel therapeutic target.

Ritu Pandey, Muhan Zhou, Shariful Islam, Baowei Chen, Natalie K Barker, Paul Langlais, Anup Srivastava, Moulun Luo, Laurence S Cooke, Eric Weterings and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
2.4field-weighted citation impact, top 9% 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, 67 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
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  8. Review
  9. Article
  10. Exploring the interactions of integrins and CEACAM6 (Review).Experimental and therapeutic medicine · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Proteomics in pancreatic cancer.Biomarker research · 2025
    Review
  16. Identification of CD66c as a potential target in gastroesophageal junction cancer for antibody-drug conjugate development.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
    Article
  17. Article
  18. Review
  19. Article
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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.

Ritu PandeyUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA. ritu@email.arizona.edu.
Muhan ZhouUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA.
Shariful IslamUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA.
Baowei ChenUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA.
Natalie K BarkerDepartment of Medicine, College of Medicine, University of Arizona, Tucson, USA.
Paul LanglaisDepartment of Medicine, College of Medicine, University of Arizona, Tucson, USA.
Anup SrivastavaDepartment of Medicine, College of Medicine, University of Arizona, Tucson, USA.
Moulun LuoDepartment of Medicine, College of Medicine, University of Arizona, Tucson, USA.
Laurence S CookeUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA.
Eric WeteringsUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA.
Daruka MahadevanUniversity of Arizona Cancer Center, University of Arizona, Tucson, USA. dmahadevan@uacc.arizona.edu.
University of Arizona · USUniversity of Arizona Cancer Center

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Teri L Bankhead · 1985 to 2026
$110.2M
NCI NIH HHS P30 CA023074
6 · The paper itself

Abstract

We investigated biomarker CEACAM6, a highly abundant cell surface adhesion receptor that modulates the extracellular matrix (ECM) in pancreatic ductal adenocarcinoma (PDA). The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) RNA-Seq data from PDA patients were analyzed for CEACAM6 expression and evaluated for overall survival, association, enrichment and correlations. A CRISPR/Cas9 Knockout (KO) of CEACAM6 in PDA cell line for quantitative proteomics, mitochondrial bioenergetics and tumor growth in mice were conducted. We found CEACAM6 is over-expressed in primary and metastatic basal and classical PDA subtypes. Highest levels are in classical activated stroma subtype. CEACAM6 over-expression is universally a poor prognostic marker in KRAS mutant and wild type PDA. High CEACAM6 expression is associated with low cytolytic T-cell activity in both basal and classical PDA subtypes and correlates with low levels of T-

Indexed as

AdenocarcinomaAnimalsAntigens, CDCarcinoma, Pancreatic DuctalCell Adhesion MoleculesCell Line, TumorCell ProliferationEnergy MetabolismGene Expression Regulation, NeoplasticGPI-Linked ProteinsHeterograftsHumansMiceMitochondriaMolecular Targeted TherapyProto-Oncogene Proteins p21(ras)Antigens, CDCEACAM6 protein, humanCell Adhesion MoleculesGPI-Linked ProteinsKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID31797958
PMCPMC6893022
OpenAlexW2993073257

What OpenQuestion holds

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Registered trials

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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.