Evidence map›Paper›PMID 32160961›Full record

ArticleTranslational research : the journal of laboratory and clinical medicine2020

Amelotin is expressed in retinal pigment epithelium and localizes to hydroxyapatite deposits in dry age-related macular degeneration.

Dinusha Rajapakse, Katherine Peterson, Sanghamitra Mishra, Jianguo Fan, Joshua Lerner, Maria Campos, Graeme Wistow

Open access · greenAbstract read
In one paragraph

Article in Translational research : the journal of laboratory and clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Dinusha RajapakseSection on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Katherine PetersonSection on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Sanghamitra MishraSection on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Jianguo FanSection on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Joshua LernerSection on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Maria CamposHistopathology Core Facility, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Graeme WistowSection on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Bethesda, Maryland. Electronic address: graeme@helix.nih.gov.
National Institutes of Health · USNational Eye Institute · US

Funding

Functional Analysis of Novel Genes in Eye Development and VisionZIAEY000433 · NEI · NATIONAL EYE INSTITUTE · PI WISTOW, GRAEME J · 2009 to 2025
$18.2M
NEIBank: Est Analysis And Bioinformatics For Ocular GenomicsZIAEY000320 · NEI · NATIONAL EYE INSTITUTE · PI WISTOW, GRAEME J · 2009 to 2023
$1.5M
Intramural NIH HHS ZIA EY000433
6 · The paper itself

Abstract

Deposition of hydroxyapatite (HAP) basal to the retinal pigment epithelium (RPE) is linked to the progression of age-related macular degeneration (AMD). Serum-deprivation of RPE cells in culture mimics some features of AMD. We now show that serum-deprivation also leads to the induction of amelotin (AMTN), a protein involved in hydroxyapatite mineralization in enamel. HAP is formed in our culture model and is blocked by siRNA inhibition of AMTN expression. In situ hybridization and immunofluorescence imaging of human eye tissue show that AMTN is expressed in RPE of donor eyes with geographic atrophy ("dry" AMD) in regions with soft drusen containing HAP spherules or nodules. AMTN is not found in hard drusen, normal RPE, or donor eyes diagnosed with wet AMD. These findings suggest that AMTN is involved in formation of HAP spherules or nodules in AMD, and as such provides a new therapeutic target for slowing disease progression.

Indexed as

AgedCulture Media, Serum-FreeDental Enamel ProteinsDurapatiteGeographic AtrophyHumansRetinal Pigment EpitheliumAMTN protein, humanCulture Media, Serum-FreeDental Enamel ProteinsDurapatite

Identifiers

PMID32160961
PMCPMC7197213
OpenAlexW3008916215

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.