Evidence map›Paper›PMID 29879416›Full record

ArticleThe American journal of pathology2018

Re-Evaluating E-Cadherin and β-Catenin: A Pan-Cancer Proteomic Approach with an Emphasis on Breast Cancer.

Nicholas Borcherding, Kimberly Cole, Paige Kluz, Michael Jorgensen, Ryan Kolb, Andrew Bellizzi, Weizhou Zhang

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in The American journal of pathology, 2018. 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
1.4field-weighted citation impact, top 19% 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, 28 citations in OpenAlex.

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  10. miR-205-5p Downregulation andInternational journal of molecular sciences · 2021
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  20. Synergistic inhibitory effects ofAvicenna journal of phytomedicine
    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

7 authors at 1 institution in 1 country.

Nicholas BorcherdingDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa; Cancer Biology Graduate Program, College of Medicine, University of Iowa, Iowa City, Iowa; Medical Scientist Training Program, College of Medicine, University of Iowa, Iowa City, Iowa; Holden Comprehensive Cancer Center, College of Medicine, University of Iowa, Iowa City, Iowa.
Kimberly ColeDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa.
Paige KluzDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa; Free Radical and Radiation Biology Program, College of Medicine, University of Iowa, Iowa City, Iowa.
Michael JorgensenDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa.
Ryan KolbDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa; Holden Comprehensive Cancer Center, College of Medicine, University of Iowa, Iowa City, Iowa.
Andrew BellizziDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa; Holden Comprehensive Cancer Center, College of Medicine, University of Iowa, Iowa City, Iowa. Electronic address: andrew-bellizzi@uiowa.edu.
Weizhou ZhangDepartment of Pathology, College of Medicine, University of Iowa, Iowa City, Iowa; Cancer Biology Graduate Program, College of Medicine, University of Iowa, Iowa City, Iowa; Medical Scientist Training Program, College of Medicine, University of Iowa, Iowa City, Iowa; Holden Comprehensive Cancer Center, College of Medicine, University of Iowa, Iowa City, Iowa; Free Radical and Radiation Biology Program, College of Medicine, University of Iowa, Iowa City, Iowa. Electronic address: weizhou-zhang@uiowa.edu.
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007337 · NIGMS · UNIVERSITY OF IOWA · PI GEYER, PAMELA K., LENTZ, STEVEN R · 1985 to 2020
$15.9M
INTERDISCIPLINARY IMMUNOLOGY TRAINING PROGRAMT32AI007260 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WU, LI · 1986 to 2023
$5.7M
Obesity, inflammation and breast cancerR01CA200673 · NCI · UNIVERSITY OF IOWA · PI ZHANG, WEIZHOU · 2016 to 2020
$1.7M
CD177 suppresses breast-cancer development by inhibiting beta-cateninR01CA203834 · NCI · UNIVERSITY OF IOWA · PI ZHANG, WEIZHOU · 2016 to 2020
$1.7M
The role of paracrine WNT5A/RYK in ErbB2-driven tumorigenesisF30CA206255 · NCI · UNIVERSITY OF IOWA · PI BORCHERDING, NICHOLAS · 2017 to 2020
$143k
NCI NIH HHS F30 CA206255NCI NIH HHS P30 CA086862NCI NIH HHS R01 CA200673NCI NIH HHS R01 CA203834NIAID NIH HHS T32 AI007260NIGMS NIH HHS T32 GM007337
6 · The paper itself

Abstract

E-cadherin is conventionally considered to be a good prognostic marker in cancer. The loss of E-cadherin is one of the key hallmarks of epithelial-to-mesenchymal transition, a biological process that promotes cancer cell invasiveness and metastasis. Recent evidence has cast doubt on the importance of epithelial-to-mesenchymal transition in metastasis. The availability of protein-level data in the Cancer Genome Atlas allows for the quantitative analysis of protein and prognosis. The prognostic values of E-cadherin and β-catenin were revisited across 19 cancer types, and high E-cadherin was found to correlate with good prognosis in most cancers. Conversely, higher E-cadherin and β-catenin correlated with shorter survival in invasive breast carcinoma. Stratifying breast cancers by histologic subtype revealed that the poor prognosis of E-cadherin and β-catenin proteins was characteristic of infiltrating ductal, but not lobular, carcinomas. To further corroborate the protein findings and examine cellular localization, immunohistochemistry was used for E-cadherin and β-catenin in 163 breast patient samples from the Iowa cohort. Most previous studies showing that reduced or absent E-cadherin and β-catenin was inversely associated with tumor stages in ductal carcinomas were confirmed. Taken together, these results lead us to question the prognostic values of E-cadherin and β-catenin in ductal carcinomas and indicate a complicated role of E-cadherin and β-catenin in breast cancer progression.

Indexed as

Antigens, CDbeta CateninBiomarkers, TumorBreast NeoplasmsCadherinsCarcinoma, Ductal, BreastCarcinoma, LobularFemaleHumansPrognosisProtein Array AnalysisSurvival RateAntigens, CDbeta CateninBiomarkers, TumorCadherinsCDH1 protein, humanCTNNB1 protein, human

Identifiers

PMID29879416
PMCPMC6119824
OpenAlexW2806021735

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.