Evidence map›Paper›PMID 35965684›Full record

ReviewOxidative medicine and cellular longevity2022

Genetic Susceptibility and Mechanisms Underlying the Pathogenesis of Anthracycline-Associated Cardiotoxicity.

Yonghe Ding, Ke Du, Yu-Juan Niu, Yong Wang, Xiaolei Xu

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Revolutionising Cardio-Oncology Care with Precision Genomics.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Review
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  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

5 authors at 3 institutions in 2 countries.

Yonghe DingThe Biomedical Sciences Institute of Qingdao University Qingdao (Branch of SJTU Bio-X Institutes), Qingdao University, Qingdao 266021, China.ORCID https://orcid.org/0000-0002-4531-1721
Ke DuThe Biomedical Sciences Institute of Qingdao University Qingdao (Branch of SJTU Bio-X Institutes), Qingdao University, Qingdao 266021, China.
Yu-Juan NiuThe Biomedical Sciences Institute of Qingdao University Qingdao (Branch of SJTU Bio-X Institutes), Qingdao University, Qingdao 266021, China.
Yong WangSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 10029, China.
Xiaolei XuDepartment of Biochemistry and Molecular Biology, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN 55902, USA.ORCID https://orcid.org/0000-0002-4928-3422
Qingdao University · CNBeijing University of Chinese Medicine · CNMayo Clinic in Arizona · US

Funding

Epicardial remodeling in cardiomyopathy and cardiac agingR01HL107304 · NHLBI · MAYO CLINIC ROCHESTER · PI Xiaolei Xu · 2011 to 2026
$6.6M
NHLBI NIH HHS R01 HL107304
6 · The paper itself

Abstract

Anthracyclines are chemotherapeutic agents widely used to treat a variety of cancers, and these drugs have revolutionized our management of cancer patients. The dose-dependent cardiotoxicity of anthracyclines, however, remains one of the leading causes of chemotherapy treatment-associated mortality in cancer survivors. Patient threshold doses leading to anthracycline-induced cardiotoxicity (AIC) are highly variable among affected patients. This variability is largely ascribed to genetic variants in individuals' genomes. Here, we briefly discuss the prevailing mechanisms underlying the pathogenesis of AIC, and then, we review the genetic variants, mostly identified through human genetic approaches and identified in cancer survivors. The identification of all genetic susceptibilities and elucidation of underlying mechanisms of AIC can help improve upfront risk prediction assessment for potentially severe cardiotoxicity disease and provide valuable insights into the understanding of AIC pathophysiology, which can be further leveraged to develop targeted pharmacogenetic therapies for those at high risk.

Indexed as

Antineoplastic AgentsNeoplasmsAnthracyclinesAntibiotics, AntineoplasticCardiotoxicityGenetic Predisposition to DiseaseHumansAnthracyclinesAntibiotics, AntineoplasticAntineoplastic Agents

Identifiers

PMID35965684
PMCPMC9365594
OpenAlexW4289654128

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.