Evidence map›Paper›PMID 21183474›Full record

ArticleDisease models & mechanisms2011

Transient receptor potential ion channel Trpm7 regulates exocrine pancreatic epithelial proliferation by Mg2+-sensitive Socs3a signaling in development and cancer.

Nelson S Yee, Weiqiang Zhou, I-Chau Liang

Open access · hybridAbstract read
In one paragraph

Article in Disease models & mechanisms, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 98 citations in OpenAlex.

  1. Review
  2. Article
  3. MgJournal of cellular physiology · 2025
    Article
  4. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. MgNutrients · 2021
    Review
  14. Article
  15. The Presence and Distribution of TRPM7 in the Canine Mammary Glands.Animals : an open access journal from MDPI · 2020
    Article
  16. TRP Channels in Digestive Tract Cancers.International journal of molecular sciences · 2020
    Review
  17. Review
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Nelson S YeeDivision of Hematology, Oncology, and Blood & Marrow Transplantation, Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA. nelson-yee@uiowa.edu
Weiqiang Zhou
I-Chau Liang
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
ZEBRAFISH INTERNATIONAL RESOURCE CENTERP40RR012546 · NCRR · UNIVERSITY OF OREGON · PI WESTERFIELD, MONTE · 1998 to 2011
$21.9M
Analysis of zebrafish exocrine pancreas developmentK08DK060529 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI YEE, NELSON SHU-SANG · 2002 to 2006
$648k
Cloning of Zebrafish exocrine pancreas mutantR03DK071960 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI YEE, NELSON SHU-SANG · 2005 to 2006
$151k
NCI NIH HHS P30 CA 086862NCI NIH HHS P30 CA086862NCRR NIH HHS P40 RR012546NCRR NIH HHS P40 RR12546NIDDK NIH HHS K08 DK 060529NIDDK NIH HHS K08 DK060529NIDDK NIH HHS R03 DK 071960NIDDK NIH HHS R03 DK071960
6 · The paper itself

Abstract

Genetic analysis of pancreatic development has provided new insights into the mechanisms underlying the formation of exocrine pancreatic neoplasia. Zebrafish sweetbread (swd) mutants develop hypoplastic acini and dysmorphic ducts in the exocrine pancreas, with impeded progression of cell division cycle and of epithelial growth. Positional cloning and allelic complementation have revealed that the swd mutations affect the transient receptor potential melastatin-subfamily member 7 (trpm7) gene, which encodes a divalent cation-permeable channel with kinase activity. Supplementary Mg(2+) partially rescued the exocrine pancreatic defects of the trpm7 mutants by improving cell-cycle progression and growth and repressing the suppressor of cytokine signaling 3a (socs3a) gene. The role of Socs3a in Trpm7-mediated signaling is supported by the findings that socs3a mRNA level is elevated in the trpm7 mutants, and antisense inhibition of socs3a expression improved their exocrine pancreatic growth. TRPM7 is generally overexpressed in human pancreatic adenocarcinoma. TRPM7-deficient cells are impaired in proliferation and arrested in the G0-G1 phases of the cell division cycle. Supplementary Mg(2+) rescued the proliferative defect of the TRPM7-deficient cells. Results of this study indicate that Trpm7 regulates exocrine pancreatic development via the Mg(2+)-sensitive Socs3a pathway, and suggest that aberrant TRPM7-mediated signaling contributes to pancreatic carcinogenesis.

Indexed as

AllelesAnimalsCell CycleCell Cycle ProteinsCell ProliferationEpithelial CellsGene Expression Regulation, NeoplasticGenetic LociHumansMagnesiumMutationOligonucleotides, AntisensePancreas, ExocrinePancreatic NeoplasmsProtein Serine-Threonine KinasesSequence Homology, Amino AcidCell Cycle ProteinsMagnesiumOligonucleotides, AntisenseProtein Serine-Threonine Kinasessocs3a protein, zebrafishSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling ProteinsTRPM7 protein, humanTrpm7 protein, zebrafishTRPM Cation ChannelsZebrafish Proteins

Identifiers

PMID21183474
PMCPMC3046099
OpenAlexW2163323412

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.