Evidence map›Paper›PMID 31767037›Full record

ArticleCell communication and signaling : CCS2019

S100P is a molecular determinant of E-cadherin function in gastric cancer.

Patrícia Carneiro, Ana Margarida Moreira, Joana Figueiredo, Rita Barros, Patrícia Oliveira, Maria Sofia Fernandes, Anabela Ferro, Raquel Almeida, Carla Oliveira, Fátima Carneiro and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 32% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. [Expression of S100P in Lung Adenocarcinoma and Its Clinical Significance].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2026
    Article
  3. Article
  4. Review
  5. Molecular and Clinicopathologic Impact of GNAS Variants Across Solid Tumors.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  6. Prognostic Value of S100 Family mRNA Expression in Hepatocellular Carcinoma.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Article
  7. Article
  8. Review
  9. The role of PI3K/AKT signaling pathway in gallbladder carcinoma.American journal of translational research · 2022
    Review
  10. Article
  11. Article
  12. Genetic and Epigenetic Alterations ofPharmaceuticals (Basel, Switzerland) · 2021
    Article
  13. The Autophagy Machinery Contributes to E-cadherin Turnover in Breast Cancer.Frontiers in cell and developmental biology · 2020
    Article
  14. 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

14 authors at 1 institution in 1 country.

Patrícia CarneiroInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Ana Margarida MoreiraInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Joana FigueiredoInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Rita BarrosInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Patrícia OliveiraInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Maria Sofia FernandesInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Anabela FerroInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Raquel AlmeidaInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Carla OliveiraInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Fátima CarneiroInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Fernando SchmittInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Joana ParedesInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Sérgia VelhoInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal.
Raquel SerucaInstituto de Investigação e Inovação em Saúde (i3S), Epithelial Interactions in Cancer Group, Rua Alfredo Allen 208, 4200-135, Porto, Portugal. rseruca@ipatimup.pt.ORCID 0000-0002-8851-4166
Universidade do Porto · PT

Funding

EBV GENOME EXPRESSION:LOCALIZATION OF SPECIFIC FUNCTIONSR01CA030356 · NCI · JOHNS HOPKINS UNIVERSITY · PI HAYWARD, S DIANE · 1986 to 2009
$3.3M
VIRUS INDUCED MYELOID LEUKEMIAR01CA030383 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BOETTIGER, DAVID E · 1985 to 1990
–
EBV GENOME EXPRESSION:LOCALIZATION OF SPECIFIC FUNCTIONSR37CA030356 · NCI · JOHNS HOPKINS UNIVERSITY · PI HAYWARD, S DIANE · 1988 to 1995
–
6 · The paper itself

Abstract

backgroundE-cadherin has been awarded a key role in the aetiology of both sporadic and hereditary forms of gastric cancer. In this study, we aimed to identify molecular interactors that influence the expression and function of E-cadherin associated to cancer.

methodsA data mining approach was used to predict stomach-specific candidate genes, uncovering S100P as a key candidate. The role of S100P was evaluated through in vitro functional assays and its expression was studied in a gastric cancer tissue microarray (TMA).

resultsS100P was found to contribute to a cancer pathway dependent on the context of E-cadherin function. In particular, we demonstrated that S100P acts as an E-cadherin positive regulator in a wild-type E-cadherin context, and its inhibition results in decreased E-cadherin expression and function. In contrast, S100P is likely to be a pro-survival factor in gastric cancer cells with loss of functional E-cadherin, contributing to an oncogenic molecular program. Moreover, expression analysis in a gastric cancer TMA revealed that S100P expression impacts negatively among patients bearing Ecad

conclusionsWe propose that S100P has a dual role in gastric cancer, acting as an oncogenic factor in the context of E-cadherin loss and as a tumour suppressor in a functional E-cadherin setting. The discovery of antagonist effects of S100P in different E-cadherin contexts will aid in the stratification of gastric cancer patients who may benefit from S100P-targeted therapies.

Indexed as

CadherinsCalcium-Binding ProteinsHumansNeoplasm ProteinsSignal TransductionStomach NeoplasmsTumor Cells, CulturedCadherinsCalcium-Binding ProteinsNeoplasm ProteinsS100P protein, humanE-cadherinGastric cancerPrognosisS100PSurvival

Identifiers

PMID31767037
PMCPMC6878717
OpenAlexW2989770620

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.