Evidence map›Paper›PMID 28903370›Full record

ArticleOncotarget2017

Human mesenchymal stem cells preferentially migrate toward highly oncogenic human hepatocellular carcinoma cells with activated EpCAM signaling.

Berwini Endaya, Shou P Guan, Jennifer P Newman, Hung Huynh, Kian C Sia, Siao T Chong, Catherine Y L Kok, Alexander Y F Chung, Bin B Liu, Kam M Hui and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Shedding light on the EpCAM: An overview.Journal of cellular physiology · 2019
    Review
  6. Article
  7. Review
  8. 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

11 authors at 5 institutions in 3 countries.

Berwini Endaya *Division of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Shou P Guan *Division of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Jennifer P NewmanDivision of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Hung HuynhDivision of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Kian C SiaDivision of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Siao T ChongDivision of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Catherine Y L KokDivision of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
Alexander Y F ChungDepartment of General Surgery, Singapore General Hospital, Singapore City, Singapore.
Bin B LiuLiver Cancer Institute of Fudan University, Shanghai, China.
Kam M HuiDepartment of Biochemistry, National University of Singapore, Singapore City, Singapore.
Paula Y P LamDivision of Cellular and Molecular Research, National Cancer Centre, Singapore City, Singapore.
National Cancer Centre Singapore · SGDuke-NUS Medical School · SGFudan University Shanghai Cancer Center · CNInstitute of Molecular and Cell Biology · SGSingapore General Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial cell adhesion molecule (EpCAM) is a type I transmembrane glycoprotein that is regarded as one of the markers for tumor initiating cells (TIC) in human hepatocellular carcinoma (HCC). Much work has been directed towards targeting these TICs as a mean of placing these master regulators of cell proliferation and drug resistance under control. Human bone marrow-derived mesenchymal stem cells are known to exhibit an innate property of tumor tropism. However, the possible relationship between MSC and TIC is not well understood. In this study, we show that MSC migration to HCC can be effectively inhibited by TACE and γ-secretase inhibitors that stop the activation of EpCAM signaling event. Silencing of EpCAM expression through siRNA and antibody approaches also resulted in impaired MSC migration. By contrast, increase levels of EpICD proteins in HCC cells and HCC mouse xenografts resulted in enhanced MSC migration. Taken together, these findings show that MSC is drawn to the more oncogenic population of HCC, and could potentially serve as a cell-based carrier of therapeutic genes to target EpICD-enriched hepatic tumor cells.

Indexed as

EpCAM signalinghuman bone marrow-derived MSChuman hepatocellular carcinomatumor tropism

Identifiers

PMID28903370
PMCPMC5589609
OpenAlexW2610508262

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.