Evidence map›Paper›PMID 17540362›Full record

ArticleDevelopmental biology2007

PTEN modulates GDNF/RET mediated chemotaxis and branching morphogenesis in the developing kidney.

Doyeob Kim, Gregory R Dressler

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Developmental Hypoxia Enhances Kidney Organoid Complexity and Maturity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  3. Article
  4. Review
  5. Review
  6. Hallmarks of RET and Co-occuring Genomic Alterations inMolecular cancer therapeutics · 2021
    Review
  7. Organ-Specific Branching Morphogenesis.Frontiers in cell and developmental biology · 2021
    Review
  8. Article
  9. Article
  10. Review
  11. The GDNF Family: A Role in Cancer?Neoplasia (New York, N.Y.) · 2018
    Review
  12. Article
  13. Article
  14. Phosphatidylinositol 3-kinase signaling determines kidney size.The Journal of clinical investigation · 2015
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  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

2 authors at 1 institution in 1 country.

Doyeob KimDepartment of Pathology, University of Michigan, MSRB1, BSRB 2049, 109 Zina Pitcher Dr., Ann Arbor, MI 48109, USA.
Gregory R Dressler
University of Michigan–Ann Arbor · US

Funding

Cell Signaling in Developing EpitheliaR01DK062914 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DRESSLER, GREGORY R · 2003 to 2010
$1.8M
NIDDK NIH HHS DK062914NIDDK NIH HHS R01 DK062914
6 · The paper itself

Abstract

The RET receptor tyrosine kinase is activated by GDNF and controls outgrowth and invasion of the ureteric bud epithelia in the developing kidney. In renal epithelial cells and in enteric neuronal precursor cells, activation of RET results in chemotaxis as Ret expressing cells invade the surrounding GDNF expressing tissue. One potential downstream signaling pathway governing RET mediated chemotaxis may require phosphatidylinositol 3-kinase (PI3K), which generates PI(3,4,5) triphosphate. The PTEN tumor suppressor gene encodes a protein and lipid phosphatase that regulates cell growth, apoptosis and many other cellular processes. PTEN helps regulate cellular chemotaxis by antagonizing the PI3K signaling pathway through dephosphorylation of phosphotidylinositol triphosphates. In this report, we show that PTEN suppresses RET mediated cell migration and chemotaxis in cell culture assays, that RET activation results in asymmetric localization of inositol triphosphates and that loss of PTEN affects the pattern of branching morphogenesis in developing mouse kidneys. These data suggest a critical role for the PI3K/PTEN axis in shaping the pattern of epithelial branches in response to RET activation.

Indexed as

AnimalsCell LineCell MovementChemotaxisDogsGlial Cell Line-Derived Neurotrophic FactorGreen Fluorescent ProteinsKidneyMiceMice, TransgenicMorphogenesisMutationPhosphatidylinositol 3-KinasesPhosphatidylinositol PhosphatesProto-Oncogene Proteins c-retPTEN PhosphohydrolaseGlial Cell Line-Derived Neurotrophic FactorGreen Fluorescent Proteinsphosphatidylinositol 3,4,5-triphosphatePhosphatidylinositol 3-KinasesPhosphatidylinositol PhosphatesProto-Oncogene Proteins c-retPTEN PhosphohydrolaseRecombinant Proteins

Identifiers

PMID17540362
PMCPMC2129124
OpenAlexW1998366631

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.