Evidence map›Paper›PMID 34018656›Full record

ArticleAging cell2021

Age-related telomere attrition causes aberrant gene expression in sub-telomeric regions.

Xiao Dong, Shixiang Sun, Lei Zhang, Seungsoo Kim, Zhidong Tu, Cristina Montagna, Alexander Y Maslov, Yousin Suh, Tao Wang, Judith Campisi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Observational
  7. Increased cell senescence in human metabolic disorders.The Journal of clinical investigation · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

11 authors at 4 institutions in 3 countries.

Xiao DongDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0001-9987-5760
Shixiang SunDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0001-5499-2963
Lei ZhangDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Seungsoo KimDepartment of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY, USA.
Zhidong TuDepartment of Genetics and Genomic Sciences, Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine Mount Sinai, New York, NY, USA.
Cristina MontagnaDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Alexander Y MaslovDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Yousin SuhDepartment of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY, USA.
Tao WangDepartment of Epidemiology & Population Health, Albert Einstein College of Medicine, Bronx, NY, USA.
Judith CampisiBuck Institute for Research on Aging, Novato, CA, USA.ORCID 0000-0001-6858-9462
Jan VijgDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine · USColumbia University Irving Medical Center · USBuck Institute for Research on Aging · USIcahn School of Medicine at Mount Sinai · US

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
The role of hyaluronan in longevity and cancer resistance of longest-lived rodentP01AG047200 · NIA · UNIVERSITY OF ROCHESTER · PI JAN VIJG · 2014 to 2026
$36.9M
Validation and characterization of the identified variants associated with human longevity in mouse modelsU19AG056278 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Zhengdong Zhang · 2017 to 2026
$24.5M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
Human tissue specific age-related gene expression changes, their genetic regulations and the link to human diseasesR01AG055501 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI TU, ZHIDONG · 2018 to 2022
$2.2M
Computational evaluation of the causal role of somatic mutations in human agingR00AG056656 · NIA · UNIVERSITY OF MINNESOTA · PI DONG, XIAO · 2021 to 2023
$747k
Computational evaluation of the causal role of somatic mutations in human agingK99AG056656 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DONG, XIAO · 2018 to 2019
$272k
NIA NIH HHS K99 AG056656NIA NIH HHS P01 AG017242NIA NIH HHS P01 AG047200NIA NIH HHS P30 AG038072NIA NIH HHS R00 AG056656NIA NIH HHS R01 AG055501NIA NIH HHS U19 AG056278
6 · The paper itself

Abstract

Telomere attrition has been proposed as a biomarker and causal factor in aging. In addition to causing cellular senescence and apoptosis, telomere shortening has been found to affect gene expression in subtelomeric regions. Here, we analyzed the distribution of age-related differentially expressed genes from the GTEx RNA sequencing database of 54 tissue types from 979 human subjects and found significantly more upregulated than downregulated genes in subtelomeric regions as compared to the genome-wide average. Our data demonstrate spatial relationships between telomeres and gene expression in aging.

Indexed as

AdultAgedAgingCellular SenescenceFemaleGene ExpressionHumansMaleMiddle AgedTelomereYoung Adultaginggene expressiontelomere shortening

Identifiers

PMID34018656
PMCPMC8208793
OpenAlexW3162051090

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.