Evidence map›Paper›PMID 31561739›Full record

ReviewAnnual review of pharmacology and toxicology2020

Targeting the Trafficking of Kidney Water Channels for Therapeutic Benefit.

Pui W Cheung, Richard Bouley, Dennis Brown

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of pharmacology and toxicology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-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

28 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Expanding Mechanistic Insights into Urinary Concentrating Ability.Journal of the American Society of Nephrology : JASN · 2025
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Genome-Engineered mpkCCDc14 Cells as a New Resource for Studying AQP2.International journal of molecular sciences · 2023
    Article
  12. Metabolomic Analysis ofPharmaceuticals (Basel, Switzerland) · 2023
    Article
  13. Aquaporins in Cardiovascular System.Advances in experimental medicine and biology · 2023
    Article
  14. LRBA is essential for urinary concentration and body water homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

3 authors at 2 institutions in 1 country.

Pui W CheungCenter for Systems Biology, Program in Membrane Biology, and Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA; email: Brown.Dennis@mgh.harvard.edu.
Richard BouleyCenter for Systems Biology, Program in Membrane Biology, and Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA; email: Brown.Dennis@mgh.harvard.edu.
Dennis BrownCenter for Systems Biology, Program in Membrane Biology, and Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA; email: Brown.Dennis@mgh.harvard.edu.
Center for Systems Biology · USHarvard University · US

Funding

Transgenic CoreP30DK057521 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KAHN, BARBARA B. · 2000 to 2019
$31.4M
Cell Biology of Vasopressin-induced Water Channels-Research SupplementR01DK096586 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Dennis Brown · 2012 to 2026
$7.3M
Characterization of Novel Signaling Pathways Involved in Water Balance DisordersK08DK115901 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHEUNG, PUI WEN · 2018 to 2022
$919k
NIDDK NIH HHS K08 DK115901NIDDK NIH HHS P30 DK057521NIDDK NIH HHS R01 DK096586
6 · The paper itself

Abstract

The ability to regulate water movement is vital for the survival of cells and organisms. In addition to passively crossing lipid bilayers by diffusion, water transport is also driven across cell membranes by osmotic gradients through aquaporin water channels. There are 13 aquaporins in human tissues, and of these, aquaporin-2 (AQP2) is the most highly regulated water channel in the kidney: The expression and trafficking of AQP2 respond to body volume status and plasma osmolality via the antidiuretic hormone, vasopressin (VP). Dysfunctional VP signaling in renal epithelial cells contributes to disorders of water balance, and research initially focused on regulating the major cAMP/PKA pathway to normalize urine concentrating ability. With the discovery of novel and more complex signaling networks that regulate AQP2 trafficking, promising therapeutic targets have since been identified. Several strategies based on data from preclinical studies may ultimately translate to the care of patients with defective water homeostasis.

Indexed as

AnimalsAquaporin 2Cell MembraneCyclic AMPCyclic AMP-Dependent Protein KinasesHumansKidneyNeurophysinsProtein PrecursorsSignal TransductionVasopressinsWaterWater-Electrolyte BalanceWater-Electrolyte ImbalanceAquaporin 2AVP protein, humanCyclic AMPCyclic AMP-Dependent Protein KinasesNeurophysinsProtein PrecursorsVasopressinsWateraquaporin-2collecting duct principal cellsendocytosisexocytosisurine concentrationvasopressin receptor type 2

Identifiers

PMID31561739
PMCPMC7334826
OpenAlexW2975171073

What OpenQuestion holds

Textmetadata
LicenceTDM
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.