Evidence map›Paper›PMID 27822417›Full record

ArticleAmerican journal of cancer research2016

Tumor endothelial cells promote metastasis and cancer stem cell-like phenotype through elevated Epiregulin in esophageal cancer.

Lichao Sun, Jian Pan, Long Yu, Huiqi Liu, Xiong Shu, Lixin Sun, Jinning Lou, Zhihua Yang, Yuliang Ran

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  5. A NovelClinical Medicine Insights. Oncology · 2024
    Article
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  18. Cancer stem cells as key drivers of tumour progression.Journal of biomedical science · 2018
    Review
  19. 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

9 authors at 3 institutions in 1 country.

Lichao SunState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Jian PanDepartment of Hematology and Oncology, Children's Hospital of Soochow University Suzhou, Jiangsu, People's Republic of China.
Long YuState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Huiqi LiuState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Xiong ShuState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Lixin SunState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Jinning LouInstitute of Clinical Medical Sciences, China-Japan Friendship Hospital Beijing, People's Republic of China.
Zhihua YangState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Yuliang RanState Key Laboratory of Molecular Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College Beijing, People's Republic of China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNChina-Japan Friendship Hospital · CNSoochow University · CN

Funding

The Role of mGluR5 Receptors in Extinction Learning of Alcohol CuesR00AA020537 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GASS, JUSTIN T · 2013 to 2015
$732k
The Role of mGluR5 Receptors in Extinction Learning of Alcohol CuesK99AA020537 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GASS, JUSTIN T · 2011 to 2012
$272k
NIAAA NIH HHS K99 AA020537NIAAA NIH HHS R00 AA020537
6 · The paper itself

Abstract

Tumor endothelial cells have been found to be associated with metastasis and cancer progression. In this study, we reported that human esophageal cancer endothelial cells (HECEC), unlike corresponding human esophageal normal endothelial cells (HENEC) displayed several distinct feature couple with unique gene expression profile. Further studies showed that HECEC can enhance migration, invasion and self-renewal properties of esophageal carcinoma cell in vitro by a direct cell-cell interaction. In vivo assay demonstrated that HECEC could significantly enhance the invasion and lung metastasis of esophageal cancer cells. To elucidate the molecular mechanisms of HECEC in esophageal carcinoma progression, we employed the microarray to analyze the gene expression profiles before and after treating with HECEC, HENEC or conditioned meium from HECEC. Among the highly expressed HECEC-regulated genes, we focused on Epiregulin (EREG). Further studies demonstrated that overexpression of EREG in EC9706 or Kyse30 cells can induce actin reorganization, sphere formation ability and a significantly enrichment of CD44

Indexed as

cancer stem cellCD44EREGEsophageal cancermetastasistumor endothelial cells

Identifiers

PMID27822417
PMCPMC5088291
OpenAlexW2567006178

What OpenQuestion holds

Textmetadata
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Registered trials

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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.