Evidence map›Paper›PMID 28874057›Full record

ReviewAntioxidants & redox signaling2018

Emerging Omics Approaches in Aging Research.

Jared S Lorusso, Oleg A Sviderskiy, Vyacheslav M Labunskyy

Abstract readReview
In one paragraph

Review in Antioxidants & redox signaling, 2018. 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
–field-weighted citation impact
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.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. A Deep-Learning Proteomic-Scale Approach for Drug Design.Pharmaceuticals (Basel, Switzerland) · 2021
    Article
  8. Article
  9. Review
  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

3 authors.

Jared S Lorusso1 Department of Dermatology, Boston University School of Medicine , Boston, Massachusetts.
Oleg A Sviderskiy2 Department of Ecology and Life Safety, Samara National Research University , Samara, Russia .
Vyacheslav M Labunskyy1 Department of Dermatology, Boston University School of Medicine , Boston, Massachusetts.

Funding

Molecular mechanisms of translational regulation in agingR01AG058713 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LABUNSKYY, VYACHESLAV M · 2019 to 2023
$2.9M
Molecular mechanisms of translational regulation in agingR56AG054566 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LABUNSKYY, VYACHESLAV M · 2017 to 2018
$765k
Endoplasmic Reticulum Thiol Redox State and Unfolded Protein Response in AgingR00AG040191 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LABUNSKYY, VYACHESLAV M · 2014 to 2016
$723k
Endoplasmic Reticulum Thiol Redox State and Unfolded Protein Response in AgingK99AG040191 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LABUNSKYY, VYACHESLAV M · 2012 to 2013
$262k
NIA NIH HHS K99 AG040191NIA NIH HHS R00 AG040191NIA NIH HHS R01 AG058713NIA NIH HHS R56 AG054566
6 · The paper itself

Abstract

significanceAging is a complex trait that is influenced by a combination of genetic and environmental factors. Although many cellular and physiological changes have been described to occur with aging, the precise molecular causes of aging remain unknown. Given the biological complexity and heterogeneity of the aging process, understanding the mechanisms that underlie aging requires integration of data about age-dependent changes that occur at the molecular, cellular, tissue, and organismal levels. Recent Advances: The development of high-throughput technologies such as next-generation sequencing, proteomics, metabolomics, and automated imaging techniques provides researchers with new opportunities to understand the mechanisms of aging. Using these methods, millions of biological molecules can be simultaneously monitored during the aging process with high accuracy and specificity. CRITICAL ISSUES: Although the ability to produce big data has drastically increased over the years, integration and interpreting of high-throughput data to infer regulatory relationships between biological factors and identify causes of aging remain the major challenges. In this review, we describe recent advances and survey emerging omics approaches in aging research. We then discuss their limitations and emphasize the need for the further development of methods for the integration of different types of data. FUTURE DIRECTIONS: Combining omics approaches and novel methods for single-cell analysis with systems biology tools would allow building interaction networks and investigate how these networks are perturbed with aging and disease states. Together, these studies are expected to provide a better understanding of the aging process and could provide insights into the pathophysiology of many age-associated human diseases. Antioxid. Redox Signal. 29, 985-1002.

Indexed as

Biomedical ResearchComputational BiologyAgingAnimalsHumansagingmetabolomicsnext-generation sequencingproteomicssystems biologytranslational regulation

Identifiers

PMID28874057
PMCPMC6104250

What OpenQuestion holds

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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.