Evidence map›Paper›PMID 32819319›Full record

ArticleBMC cancer2020

MEIS1 promotes expression of stem cell markers in esophageal squamous cell carcinoma.

Selma Zargari, Shabnam Negahban Khameneh, Abolfazl Rad, Mohammad Mahdi Forghanifard

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The impact ofAnimal cells and systems · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. In Search of a Unifying Concept in Human Diseases.Diseases (Basel, Switzerland) · 2021
    Article
  12. 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

4 authors at 3 institutions in 1 country.

Selma ZargariMedical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Shabnam Negahban KhamenehDepartment of Biology, Damghan branch, Islamic Azad University, P.O.Box: 3671639998, Cheshmeh-Ali Boulevard, Sa'dei Square, Damghan, Islamic Republic of Iran.
Abolfazl RadCellular and Molecular Research center, Sabzevar University of Medical Sciences, Sabzevar, Iran.
Mohammad Mahdi ForghanifardDepartment of Biology, Damghan branch, Islamic Azad University, P.O.Box: 3671639998, Cheshmeh-Ali Boulevard, Sa'dei Square, Damghan, Islamic Republic of Iran. forghanifard@gmail.com.ORCID http://orcid.org/0000-0002-7691-6897
Islamic Azad University, Damghan Branch · IRMashhad University of Medical Sciences · IRSabzevar University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMEIS1 (Myeloid ecotropic viral integration site 1) as a homeobox (HOX) transcription factor plays regulatory roles in a variety of cellular processes including development, differentiation, survival, apoptosis and hematopoiesis, as well as stem cell regulation. Few studies have established pluripotency and self-renewal regulatory roles for MEIS1 in human esophageal squamous cell carcinoma (ESCC), and our aim in this study was to evaluate the functional correlation between MEIS1 and the stemness markers in ESCC patients and cell line KYSE-30.

methodsExpression pattern of MEIS1 and SALL4 gene expression was analyzed in different pathological features of ESCC patients. shRNA in retroviral vector was used for constantly silencing of MEIS1 mRNA in ESCC line (KYSE-30). Knockdown of MEIS1 gene and the expression pattern of selected stemness markers including SALL4, OCT4, BMI-1, HIWI, NANOG, PLK1, and KLF4 were evaluated using real-time PCR.

resultsSignificant correlations were observed between MEIS1 and stemness marker SALL4 in different early pathological features of ESCC including non-invaded tumors, and the tumors with primary stages of progression. Retroviral knockdown of MEIS1 in KYSE-30 cells caused a noteworthy underexpression of both MEIS1 and major involved markers in stemness state of the cells including SALL4, OCT4, BMI-1, HIWI and KLF4.

conclusionsThe results highlight the important potential role of MEIS1 in modulating stemness properties of ESCCs and cells KYSE-30. These findings may confirm the linkage between MEIS1 and self-renewal capacity in ESCC and support probable oncogenic role for MEIS1 in the disease.

Indexed as

AgedBiomarkers, TumorCell Line, TumorCell Self RenewalDisease ProgressionEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaEsophagusFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHEK293 CellsHumansKruppel-Like Factor 4MaleMiddle AgedBiomarkers, TumorKLF4 protein, humanKruppel-Like Factor 4MEIS1 protein, humanMyeloid Ecotropic Viral Integration Site 1 ProteinESCCKYSE-30MEIS1Self-renewalStemness markers

Identifiers

PMID32819319
PMCPMC7441725
OpenAlexW3060959467

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.