Evidence map›Paper›PMID 27482645›Full record

ArticleHepatology (Baltimore, Md.)2016

Liver protects metastatic prostate cancer from induced death by activating E-cadherin signaling.

Bo Ma, Sarah E Wheeler, Amanda M Clark, Diana L Whaley, Min Yang, Alan Wells

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

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  17. A Perspective on Therapeutic Pan-Resistance in Metastatic Cancer.International journal of molecular sciences · 2020
    Review
  18. Review
  19. Article
  20. Adult Stem Cell Functioning in the Tumor Micro-Environment.International journal of molecular sciences · 2019
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Bo MaDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA.
Sarah E WheelerDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA.
Amanda M ClarkDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA.
Diana L WhaleyDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA.
Min YangDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA.
Alan WellsDepartment of Pathology, University of Pittsburgh, Pittsburgh, PA. wellsa@upmc.edu.
VA Pittsburgh Healthcare System · USUniversity of Pittsburgh · USUPMC Hillman Cancer Center · US

Funding

Probing the Role of the Tumor Microenvironment on Mechanistic Biomarkers for Chemotherapeutic ResistanceUH3TR000496 · NCATS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRIFFITH, LINDA G · 2014 to 2016
$3.5M
Molecular Regulation of Cancer ProgressionI01BX001017 · VA · VETERANS HEALTH ADMINISTRATION · PI WELLS, ALAN · 2012 to 2015
–
Molecular Regulation of Breast Cancer ProgressionI01BX003368 · VA · VETERANS HEALTH ADMINISTRATION · PI WELLS, ALAN · 2016 to 2023
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BLRD VA I01 BX001017BLRD VA I01 BX003368NCATS NIH HHS UH3 TR000496
6 · The paper itself

Abstract

Liver is one of the most common sites of cancer metastasis. Once disseminated, the prognosis is poor as these tumors often display generalized chemoresistance, particularly for carcinomas that derive not from the aerodigestive tract. When these cancers seed the liver, the aggressive cells usually undergo a mesenchymal to epithelial reverting transition that both aids colonization and renders the tumor cells chemoresistant. In vitro studies demonstrate that hepatocytes drive this phenotypic shift. However, the in vivo evidence and the molecular signals that protect these cells from induced death are yet to be defined. Herein, we report that membrane surface E-cadherin-expressing prostate cancer cells were resistant to cell death by chemotherapeutic drugs but E-cadherin null cells or those expressing E-cadherin only in the cytoplasm were sensitive to death signals and chemotherapies both in vitro and in vivo. While cell-cell E-cadherin ligandation reduced mitogenesis, this chemoprotection was proliferation-independent as killing of both 5-ethynyl-2'-deoxyuridine-positive (or Ki67

conclusionLiver microenvironment-driven phenotypic switching of carcinoma cells and subsequent survival signaling results in activation of canonical survival pathways that protect the disseminated prostate cancer liver micrometastases in a proliferation-independent manner, and these pathways can be targeted as an adjuvant treatment to improve the efficacy of traditional chemotherapeutics (Hepatology 2016;64:1725-1742).

Indexed as

AnimalsCadherinsCell DeathHumansLiverMaleMiceNeoplasm MetastasisProstatic NeoplasmsSignal TransductionTumor Cells, CulturedCadherins

Identifiers

PMID27482645
PMCPMC5074910
OpenAlexW2498518809

What OpenQuestion holds

Textmetadata
LicenceTDM
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.