Evidence map›Paper›PMID 35939707›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

DARPP32, a target of hyperactive mTORC1 in the retinal pigment epithelium.

Jiyang Cai, Christopher Litwin, Rui Cheng, Jian-Xing Ma, Yan Chen

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. 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
1.2field-weighted citation impact, top 22% 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, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Role of LIPIN 1 in regulating metabolic homeostasis in the retinal pigment epithelium.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  6. Article
  7. Interleukin-17-mediated protective cytokine signaling against degeneration of the retinal pigment epithelium.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Lysosomes in retinal health and disease.Trends in neurosciences · 2023
    Review
  9. Article
  10. 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

5 authors at 3 institutions in 1 country.

Jiyang CaiDepartment of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104.ORCID 0000-0003-4755-5452
Christopher LitwinDean McGee Eye Institute, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104.
Rui ChengDepartment of Biochemistry, Wake Forest University Health Sciences, Winston Salem, NC 27157.
Jian-Xing MaDepartment of Biochemistry, Wake Forest University Health Sciences, Winston Salem, NC 27157.
Yan ChenDean McGee Eye Institute, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104.ORCID 0000-0001-8451-5498
Dean McGee Eye Institute · USWake Forest University · USUniversity of Oklahoma Health Sciences Center · US

Funding

P30-CENTER CORE GRANT FOR VISION RESEARCHP30EY021725 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Michelle C Callegan, MICHAEL H ELLIOTT · 2011 to 2026
$10.5M
mTORC1-TFEB pathway in degeneration of the RPER01EY026999 · NEI · UNIVERSITY OF TEXAS MED BR GALVESTON · PI CHEN, YAN · 2016 to 2025
$3.4M
Cadmium-potentiated metabolic reprogramming in pathogenesis of lung fibrosisR01ES031980 · NIEHS · EMORY UNIVERSITY · PI GO KANG, YOUNG-MI · 2021 to 2025
$2.2M
NEI NIH HHS P30 EY021725NEI NIH HHS R01 EY026999NIEHS NIH HHS R01 ES031980
6 · The paper itself

Abstract

The mechanistic target of rapamycin (mTOR) is assembled into signaling complexes of mTORC1 or mTORC2, and plays key roles in cell metabolism, stress response, and nutrient and growth factor sensing. Accumulating evidence from human and animal model studies has demonstrated a pathogenic role of hyperactive mTORC1 in age-related macular degeneration (AMD). The retinal pigment epithelium (RPE) is a primary injury site in AMD. In mouse models of RPE-specific deletion of Tuberous sclerosis 1 (

Indexed as

Dopamine and cAMP-Regulated Phosphoprotein 32Macular DegenerationMechanistic Target of Rapamycin Complex 1Retinal Pigment EpitheliumAnimalsDisease Models, AnimalEnzyme ActivationHumansMiceRetinaSignal TransductionDopamine and cAMP-Regulated Phosphoprotein 32Mechanistic Target of Rapamycin Complex 1PPP1R1B protein, humanPpp1r1b protein, mouseage-related macular degenerationdrusenmTORC1RPE

Identifiers

PMID35939707
PMCPMC9388070
OpenAlexW4290725188

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.