Evidence map›Paper›PMID 38102454›Full record

ReviewNature aging2024

Mechanisms, pathways and strategies for rejuvenation through epigenetic reprogramming.

Andrea Cipriano, Mahdi Moqri, Sun Y Maybury-Lewis, Ryan Rogers-Hammond, Tineke Anna de Jong, Alexander Parker, Sajede Rasouli, Hans Robert Schöler, David A Sinclair, Vittorio Sebastiano

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Nature aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  3. Review
  4. Cellular senescence and aging: molecular mechanisms and convergent pathways.Cellular and molecular life sciences : CMLS · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Andrea Cipriano *Department of Obstetrics & Gynecology, Stanford School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0003-0775-3198
Mahdi Moqri *Department of Obstetrics & Gynecology, Stanford School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0001-6675-0566
Sun Y Maybury-Lewis *Department of Genetics, Harvard Medical School, Boston, MA, USA.
Ryan Rogers-HammondDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Tineke Anna de JongDepartment of Obstetrics & Gynecology, Stanford School of Medicine, Stanford University, Stanford, CA, USA.
Alexander ParkerDepartment of Obstetrics & Gynecology, Stanford School of Medicine, Stanford University, Stanford, CA, USA.
Sajede RasouliDepartment of Obstetrics & Gynecology, Stanford School of Medicine, Stanford University, Stanford, CA, USA.ORCID 0000-0002-9235-0336
Hans Robert SchölerDepartment of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID 0000-0003-2643-5136
David A SinclairDepartment of Genetics, Harvard Medical School, Boston, MA, USA. david_sinclair@hms.harvard.edu.ORCID 0000-0002-9936-436X
Vittorio SebastianoDepartment of Obstetrics & Gynecology, Stanford School of Medicine, Stanford University, Stanford, CA, USA. vsebast@stanford.edu.ORCID 0000-0002-8498-8655
California Institute for Regenerative Medicine · USHarvard University · USBrigham and Women's Hospital · USMax Planck Institute for Molecular Biomedicine · DE

Funding

Role of Sgs1 DNA helicase in telomere maintenanceR01AG019719 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SINCLAIR, DAVID A. · 2001 to 2022
$5.3M
Stanford Training Program in Aging ResearchT32AG047126 · NIA · STANFORD UNIVERSITY · PI VYJEYANTHI S PERIYAKOIL, TONY WYSS-CORAY · 2014 to 2026
$4.3M
Elucidating mechanisms of SIRT1 activationR01DK100263 · NIDDK · HARVARD MEDICAL SCHOOL · PI SINCLAIR, DAVID A. · 2016 to 2020
$2.5M
Dissecting the Molecular Role of TBX1 in the Context of Human Pharyngeal EndodermDevelopmentR01HL157139 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Vittorio Sebastiano · 2022 to 2026
$2.0M
NHLBI NIH HHS R01 HL157139NIA NIH HHS R01 AG019719NIA NIH HHS T32 AG047126NIDDK NIH HHS R01 DK100263
6 · The paper itself

Abstract

Over the past decade, there has been a dramatic increase in efforts to ameliorate aging and the diseases it causes, with transient expression of nuclear reprogramming factors recently emerging as an intriguing approach. Expression of these factors, either systemically or in a tissue-specific manner, has been shown to combat age-related deterioration in mouse and human model systems at the cellular, tissue and organismal level. Here we discuss the current state of epigenetic rejuvenation strategies via partial reprogramming in both mouse and human models. For each classical reprogramming factor, we provide a brief description of its contribution to reprogramming and discuss additional factors or chemical strategies. We discuss what is known regarding chromatin remodeling and the molecular dynamics underlying rejuvenation, and, finally, we consider strategies to improve the practical uses of epigenetic reprogramming to treat aging and age-related diseases, focusing on the open questions and remaining challenges in this emerging field.

Indexed as

Induced Pluripotent Stem CellsRejuvenationAgingAnimalsCellular ReprogrammingEpigenesis, GeneticHumansMice

Identifiers

PMID38102454
PMCPMC11058000
OpenAlexW4389786764

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.