Evidence map›Paper›PMID 23832500›Full record

ArticlePflugers Archiv : European journal of physiology2013

The role of TMEM16A (ANO1) and TMEM16F (ANO6) in cell migration.

K S Jacobsen, K Zeeberg, D R P Sauter, K A Poulsen, E K Hoffmann, A Schwab

Abstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
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

43 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Open medicine (Warsaw, Poland) · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Activation of TMEM16A CaJournal of advanced research · 2021
    Article
  12. Review
  13. Review
  14. Article
  15. The Prognostic Value and Mechanisms of TMEM16A in Human Cancer.Frontiers in molecular biosciences · 2021
    Review
  16. Review
  17. Review
  18. Review
  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

6 authors.

K S JacobsenDepartment of Biology, August Krogh Building, Universitetsparken 13, 2100, Copenhagen Ø, Denmark.
K Zeeberg
D R P Sauter
K A Poulsen
E K Hoffmann
A Schwab

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the TMEM16 family have recently been described as Ca(2+)-activated Cl(-) channels. They have been implicated in cancer and appear to be associated with poor patient prognosis. Here, we investigate the role of TMEM16 channels in cell migration, which is largely unknown. We focused on TMEM16A and TMEM16F channels that have the highest expression of TMEM16 channels in Ehrlich Lettre ascites (ELA) cells. Due to the lack of specific pharmacological modulators, we employed a miRNA approach and stably knocked down the expression of TMEM16A and TMEM16F channels, respectively. Migration analysis shows that TMEM16A KD clones are affected in their directional migration, whereas TMEM16F KD clones show a 40 % reduced rate of cell migration. Moreover, TMEM16A KD clones have a smaller projected cell area, and they are rounder than TMEM16F KD clones. The morphological changes are linearly correlated with the directionality of cells. TMEM16A and TMEM16F, thus, have an important function in cell migration-TMEM16A in directional migration, TMEM16F in determination of the speed of migration. We conclude that TMEM16A and TMEM16F channels have a distinct impact on the steering and motor mechanisms of migrating ELA cells.

Indexed as

AnimalsAnoctamin-1AnoctaminsCarcinoma, Ehrlich TumorCell MovementChloride ChannelsGene Knockdown TechniquesMicePhospholipid Transfer ProteinsANO1 protein, mouseANO6 protein, mouseAnoctamin-1AnoctaminsChloride ChannelsPhospholipid Transfer Proteins

Identifiers

PMID23832500
PMCPMC3898376

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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.