Evidence map›Paper›PMID 38141765›Full record

ArticleThe Journal of biological chemistry2024

Endolysosomal TRPML1 channel regulates cancer cell migration by altering intracellular trafficking of E-cadherin and β

Nadine Frey, Lina Ouologuem, Julia Blenninger, Wei-Xiong Siow, Julia Thorn-Seshold, Jan Stöckl, Carla Abrahamian, Thomas Fröhlich, Angelika M Vollmar, Christian Grimm and 1 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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 1 institution in 1 country.

Nadine FreyDepartment of Pharmacy, Pharmaceutical Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Lina OuologuemDepartment of Pharmacy, Pharmaceutical Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Julia BlenningerDepartment of Pharmacy, Pharmaceutical Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Wei-Xiong SiowDepartment of Pharmacy, Pharmaceutical Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Julia Thorn-SesholdDepartment of Pharmacy, Ludwig-Maximilians-University Munich, Munich, Germany.
Jan StöcklGene Center, Laboratory for Functional Genome Analysis, Ludwig Maximilians-University Munich, Munich, Germany.
Carla AbrahamianWalther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University Munich, Munich, Germany.
Thomas FröhlichGene Center, Laboratory for Functional Genome Analysis, Ludwig Maximilians-University Munich, Munich, Germany.
Angelika M VollmarDepartment of Pharmacy, Pharmaceutical Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Christian GrimmWalther-Straub-Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University Munich, Munich, Germany.
Karin BartelDepartment of Pharmacy, Pharmaceutical Biology, Ludwig-Maximilians-University Munich, Munich, Germany. Electronic address: karin.bartel@cup.uni-muenchen.de.
Ludwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis still accounts for 90% of all cancer-related death cases. An increase of cellular mobility and invasive traits of cancer cells mark two crucial prerequisites of metastasis. Recent studies highlight the involvement of the endolysosomal cation channel TRPML1 in cell migration. Our results identified a widely antimigratory effect upon loss of TRPML1 function in a panel of cell lines in vitro and reduced dissemination in vivo. As mode-of-action, we established TRPML1 as a crucial regulator of cytosolic calcium levels, actin polymerization, and intracellular trafficking of two promigratory proteins: E-cadherin and β

Indexed as

CadherinsCell MovementIntegrin beta1NeoplasmsTransient Receptor Potential ChannelsAnimalsAntigens, CDCalciumCell Line, TumorHumansLysosomesMiceNF-kappa BProtein TransportAntigens, CDCadherinsCalciumCDH1 protein, humanIntegrin beta1MCOLN1 protein, humanNF-kappa BTransient Receptor Potential Channelsadhesioncancer biologyion channellysosomemigration

Identifiers

PMID38141765
PMCPMC10825694
OpenAlexW4390064669

What Socratic 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 Socratic graph.