Evidence map›Paper›PMID 32425074›Full record

ReviewExpert review of proteomics2020

The power of proteomics to monitor senescence-associated secretory phenotypes and beyond: toward clinical applications.

Nathan Basisty, Abhijit Kale, Sandip Patel, Judith Campisi, Birgit Schilling

Open access · hybridAbstract readReview
In one paragraph

Review in Expert review of proteomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Therapeutic targeting of senescent cells in the CNS.Nature reviews. Drug discovery · 2024
    Review
  19. Article
  20. 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 1 institution in 1 country.

Nathan BasistyBuck Institute for Research on Aging, Novato , California, USA.ORCID 0000-0001-6173-1139
Abhijit KaleBuck Institute for Research on Aging, Novato , California, USA.ORCID 0000-0002-1105-6953
Sandip PatelBuck Institute for Research on Aging, Novato , California, USA.ORCID 0000-0002-0651-4438
Judith CampisiBuck Institute for Research on Aging, Novato , California, USA.ORCID 0000-0001-6858-9462
Birgit SchillingBuck Institute for Research on Aging, Novato , California, USA.ORCID 0000-0001-9907-2749
Buck Institute for Research on Aging · 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
Quantitative Proteomics to Develop Robust Senescence-Related Biomarkers for AgingU01AG060906 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI SCHILLING, BIRGIT · 2018 to 2022
$4.0M
Cellular Senescence, astrocytes and Alzheimer's diseaseR01AG051729 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI CAMPISI, JUDITH · 2016 to 2020
$2.7M
TripleTOF 5600 High Resolution Mass SpectrometerS10OD016281 · OD · BUCK INSTITUTE FOR RESEARCH ON AGING · PI GIBSON, BRADFORD WAYNE · 2013 to 2013
$597k
Quantitating, Targeting, and Phenotyping In Vivo Cellular Senescence in HumansK99AG065484 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI BASISTY, NATAN BOHDONIVICH · 2020 to 2021
$158k
NIA NIH HHS K99 AG065484NIA NIH HHS P01 AG017242NIA NIH HHS R01 AG051729NIA NIH HHS U01 AG060906NIH HHS S10 OD016281
6 · The paper itself

Abstract

introductionCellular senescence is a rapidly growing field with potential relevance for the treatment of multiple human diseases. In the last decade, cellular senescence and the senescence-associated secretory phenotype (SASP) have emerged as central drivers of aging and many chronic diseases, including cancer, neurodegeneration, heart disease and osteoarthritis. Major efforts are underway to develop drugs that selectively eliminate senescent cells (senolytics) or alter the SASP (senomorphics) to treat age-related diseases in humans. The translation of senescence-targeting therapies into humans is still in early stages. Nonetheless, it is clear that proteomic approaches will facilitate the discovery of important SASP proteins, development of senescence- and SASP-derived biomarkers, and identification of therapeutic targets for senolytic and senomorphic drugs. AREAS COVERED: We review recent proteomic studies of cellular senescence and their translational relevance and, particularly, characterization of the secretory phenotype and preclinical development of biomarkers (from 2008-2020, PubMed). We focus on emerging areas, such as the heterogeneity of senescent cells and the SASP, extracellular vesicles released by senescent cells, and validating biomarkers of aging in vivo. EXPERT OPINION: Proteomic and multi-omic approaches will be important for the development of senescence-based biomarkers to facilitate and monitor future therapeutic interventions that target senescent cells.

Indexed as

Cellular SenescenceAnimalsExosomesHumansPhenotypeProteomeProteomicsProteomeAgingbiomarkersclinical proteomicsdata-independent acquisitionplasmasecretomesenescencesenescence-associated secretory phenotypesenolyticssenomorphics

Identifiers

PMID32425074
PMCPMC7416420
OpenAlexW3027623100

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.