Evidence map›Paper›PMID 31481751›Full record

ArticleScientific reports2019

Loss of CEACAM1 is associated with poor prognosis and peritoneal dissemination of patients with gastric cancer.

Akihiro Takeuchi, Shozo Yokoyama, Mikihito Nakamori, Masaki Nakamura, Toshiyasu Ojima, Shunsuke Yamaguchi, Yasuyuki Mitani, John E Shively, Hiroki Yamaue

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 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Integration of TE Induces Cancer Specific Alternative Splicing Events.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Frontiers in genetics · 2021
    Article
  17. Article
  18. Review
  19. Joint analysis of lncRNA mCancer cell international · 2020
    Article
  20. Molecular biology and immunology of gastric cancer peritoneal metastasis.Translational gastroenterology and hepatology · 2020
    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

9 authors at 2 institutions in 2 countries.

Akihiro TakeuchiSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
Shozo YokoyamaSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan. yokoyama@wakayama-med.ac.jp.
Mikihito NakamoriSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
Masaki NakamuraSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
Toshiyasu OjimaSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
Shunsuke YamaguchiSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
Yasuyuki MitaniSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
John E ShivelyDepartment of Molecular Imaging & Therapy, Beckman Research Institute of the City of Hope, Duarte, CA, 91010, USA.
Hiroki YamaueSecond Department of Surgery, School of Medicine, Wakayama Medical University, Wakayama, 641-8510, Japan.
Wakayama Medical University · JPBeckman Research Institute

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CEACAM1 is associated with malignant potential of various cancers. The current study aims to clarify the association between carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) expression and malignant potential of gastric cancer and to address whether CEACAM1 cytoplasmic domain isoform balance modulates the properties of gastric cancer cells. Immunohistochemical analyses for CEACAM1 were performed in 235 patients with gastric cancer who underwent surgery. Risk factors for overall survival and peritoneal metastasis were calculated based on CEACAM1 expression in the gastric cancer tissue. Patients with CEACAM1 long (CEACAM1-L) or short (CEACAM1-S) cytoplasmic isoform dominance were compared with patients with null CEACAM1 expression in terms of overall survival. CEACAM1 transfected or knockdown gastric cancer cell line, NUGC3 and MKN7 cells, were examined by invasion assay and three dimensional (3D) culture, in order to clarify whether CEACAM1 modulate invasion, lumen formation and tumor growth of gastric cancer cells. Multivariate analysis demonstrated that gastric cancer without CEACAM1 is an independent prognostic factor and a risk factor for peritoneal dissemination. Patients with CEACAM1-S dominance had better prognosis than those with CEACAM1-L. CEACAM1-4L overexpression induced less invasion, more lumen formation, and less tumor growth of NUGC3 cells. CEACAM1-4S overexpression had less invasion and more lumen formations, but not less tumor growth. Knockdown of CEACAM1 expression had less invasion, but not less lumen formations of MKN7 cells. Loss of CEACAM1 is associated with poor prognosis and peritoneal dissemination of patients with gastric cancer. Expression of CEACAM1 in gastric cancer cells modulates invasiveness, lumen formation, and tumor growth.

Indexed as

Gene Expression Regulation, NeoplasticPeritoneal NeoplasmsStomach NeoplasmsAnimalsAntigens, CDCell Adhesion MoleculesCell Line, TumorDisease-Free SurvivalFemaleHumansMaleMiceMice, Inbred NODMice, SCIDNeoplasm InvasivenessNeoplasm MetastasisAntigens, CDCD66 antigensCell Adhesion MoleculesNeoplasm Proteins

Identifiers

PMID31481751
PMCPMC6722051
OpenAlexW2972097865

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.