Evidence map›Paper›PMID 11948399›Full record

ArticleOncogene2002

Metastasis-associated protein (MTA)1 enhances migration, invasion, and anchorage-independent survival of immortalized human keratinocytes.

My G Mahoney, Anisha Simpson, Monika Jost, Mariadele Noé, Csaba Kari, Deanna Pepe, Yoo Won Choi, Jouni Uitto, Ulrich Rodeck

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. HPV16-E6 Oncoprotein Activates TGF-BioMed research international · 2018
    Article
  9. Review
  10. MTA1 promotes metastasis of MPM via suppression of E-cadherin.Journal of experimental & clinical cancer research : CR · 2015
    Article
  11. Article
  12. Embryonic stem cell-specific signature in cervical cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Review
  13. MTA1 promotes nasopharyngeal carcinoma growth in vitro and in vivo.Journal of experimental & clinical cancer research : CR · 2013
    Article
  14. Modulation of cancer traits by tumor suppressor microRNAs.International journal of molecular sciences · 2013
    Review
  15. Article
  16. Article
  17. MTA1 expression correlates significantly with cigarette smoke in non-small cell lung cancer.Virchows Archiv : an international journal of pathology · 2011
    Article
  18. Bidirectional autoregulatory mechanism of metastasis-associated protein 1-alternative reading frame pathway in oncogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  19. Article
  20. 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 2 institutions in 1 country.

My G MahoneyDepartment of Dermatology and Cutaneous Biology, Jefferson Medical College, and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, PA 19107, USA. My.Mahoney@mail.tju.edu
Anisha Simpson
Monika Jost
Mariadele Noé
Csaba Kari
Deanna Pepe
Yoo Won Choi
Jouni Uitto
Ulrich Rodeck
Jefferson Institute · USThomas Jefferson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human metastasis-associated gene (MTA1), a member of the nucleosome remodeling complex with histone deacetylase activity, is frequently overexpressed in biologically aggressive epithelial neoplasms. Here, we extend this observation to squamous carcinoma cells, which express high levels of MTA1 relative to normal or immortalized keratinocytes. To address functional aspects of MTA1 expression, we established variants of human immortalized keratinocytes (HaCaT cells) by expressing MTA1 cDNA in both the sense and antisense orientations. We demonstrate that (1) forced MTA1 expression enhances migration and invasion of immortalized keratinocytes; (2) MTA1 expression is necessary but not sufficient for cell survival in the anchorage independent state; (3) MTA1 contributes to expression of the anti-apoptotic Bcl-2 family member Bcl-x(L); (4) MTA1 expression in immortalized keratinocytes depends, in part, on activation of the epidermal growth factor receptor (EGFR). These results establish that, in keratinocytes, MTA1 expression contributes to several aspects of the metastatic phenotype including survival in the anchorage independent state, migration, and invasion.

Indexed as

Cell MovementHistone DeacetylasesRepressor ProteinsAnoikisbcl-X ProteinBlotting, WesternCarcinoma, Squamous CellCell AdhesionCell DivisionErbB ReceptorsGene Expression Regulation, NeoplasticHumansKeratinocytesNeoplasm InvasivenessNeoplasm MetastasisProteinsBCL2L1 protein, humanbcl-X ProteinErbB ReceptorsHistone DeacetylasesMTA1 protein, humanProteinsProto-Oncogene Proteins c-bcl-2Repressor ProteinsRNA, MessengerTrans-Activators

Identifiers

PMID11948399
OpenAlexW2021046438

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.