Evidence map›Paper›PMID 36302155›Full record

ReviewJournal of applied physiology (Bethesda, Md. : 1985)2022

A bench to bedside perspective on anthracycline chemotherapy-mediated cardiovascular dysfunction: challenges and opportunities. A symposium review.

Zachary S Clayton, Carl J Ade, Christina M Dieli-Conwright, Hansie M Mathelier

Open access · greenAbstract readReview
In one paragraph

Review in Journal of applied physiology (Bethesda, Md. : 1985), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. 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

4 authors at 4 institutions in 1 country.

Zachary S ClaytonDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado.ORCID 0000-0003-3878-3533
Carl J AdeDepartment of Kinesiology, Kansas State University, Manhattan, Kansas.ORCID 0000-0002-1837-2342
Christina M Dieli-ConwrightDivision of Population Sciences, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Hansie M MathelierPenn Medicine, University of Pennsylvania Health System, Philadelphia, Pennsylvania.
Harvard University · USKansas State University · USUniversity of Colorado Boulder · USUniversity of Pennsylvania Health System · US

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
Translational studies of cellular senescence as a regulator of doxorubicin-mediated arterial dysfunctionK99HL159241 · NHLBI · UNIVERSITY OF COLORADO · PI CLAYTON, ZACHARY S. · 2022 to 2023
$350k
Mitochondrial oxidative stress: a target for treatment of doxorubicin-associated vascular endothelial dysfunctionF32HL151022 · NHLBI · UNIVERSITY OF COLORADO · PI CLAYTON, ZACHARY S. · 2020 to 2021
$89k
NCATS NIH HHS UL1 TR001855NHLBI NIH HHS F32 HL151022NHLBI NIH HHS K99 HL159241
6 · The paper itself

Abstract

Cardiovascular diseases (CVD) are the leading cause of death worldwide and the risk of developing CVD is markedly increased following anthracycline chemotherapy treatment. Anthracyclines are an essential component of the cancer treatment regimen used for common forms of cancer in male and female children, adolescents, young adults, and older adults. Increased CVD risk with anthracyclines occurs, in part, due to vascular dysfunction-impaired endothelial function and arterial stiffening. These features of vascular dysfunction also play a major role in other common disorders observed following anthracycline treatment, including chronic kidney disease, dementia, and exercise intolerance. However, the mechanisms by which anthracycline chemotherapy induces and sustains vascular dysfunction are incompletely understood. This budding area of biomedical research is termed cardio-oncology, which presents the unique opportunity for collaboration between physicians and basic scientists. This symposium, presented at Experimental Biology 2022, provided a timely update on this important biomedical research topic. The speakers presented observations made at levels from cells to mice to humans treated with anthracycline chemotherapeutic agents using an array of translational research approaches. The speaker panel included a diverse mix of female and male investigators and unique insight from a cardio-oncology physician-scientist. Particular emphasis was placed on challenges and opportunities in this field as well as mechanisms that could be viewed as therapeutic targets leading to novel treatment strategies.

Indexed as

Cardiovascular DiseasesNeoplasmsPolyketidesAdolescentAgedAnimalsAnthracyclinesArteriesChildFemaleHumansMaleMiceTranslational Research, BiomedicalYoung AdultAnthracyclinesPolyketidesarterial stiffnesscardio-oncologyclinical careendothelial functionvascular dysfunction

Identifiers

PMID36302155
PMCPMC9762976
OpenAlexW4307440658

What Socratic holds

Textmetadata
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 Socratic graph.