Evidence map›Paper›PMID 33438055›Full record

ReviewCellular and molecular life sciences : CMLS2021

Molecular mechanisms of doxorubicin-induced cardiotoxicity: novel roles of sirtuin 1-mediated signaling pathways.

Jie Wang A, Jingjing Zhang, Mengjie Xiao, Shudong Wang, Jie Wang B, Yuanfang Guo, Yufeng Tang, Junlian Gu

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 1% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Jie Wang ASchool of Nursing, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Jingjing ZhangDepartment of Cardiology, The First Hospital of China Medical University, Shenyang, 110016, Liaoning, China.
Mengjie XiaoSchool of Nursing, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Shudong WangDepartment of Cardiology, The First Hospital of Jilin University, Changchun, 130021, Jilin, China.
Jie Wang BSchool of Nursing, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Yuanfang GuoSchool of Nursing, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Yufeng TangDepartment of Orthopedic Surgery, The First Affiliated Hospital of Shandong First Medical University, Jinan, 250014, Shandong, China.
Junlian GuSchool of Nursing, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China. junlian_gu@sdu.edu.cn.ORCID http://orcid.org/0000-0001-8146-1260
Shandong University · CNJilin University · CNLiaoning Provincial People's Hospital · CNShandong First Medical University · CN

Funding

Jilin Science and Technology Department 20200801061GHNational Natural Science Foundation of China 81700329National Natural Science Foundation of China 81770375Qilu Young Scholar's Program of Shandong University 21330089963007
6 · The paper itself

Abstract

Doxorubicin (DOX) is an anthracycline chemotherapy drug used in the treatment of various types of cancer. However, short-term and long-term cardiotoxicity limits the clinical application of DOX. Currently, dexrazoxane is the only approved treatment by the United States Food and Drug Administration to prevent DOX-induced cardiotoxicity. However, a recent study found that pre-treatment with dexrazoxane could not fully improve myocardial toxicity of DOX. Therefore, further targeted cardioprotective prophylaxis and treatment strategies are an urgent requirement for cancer patients receiving DOX treatment to reduce the occurrence of cardiotoxicity. Accumulating evidence manifested that Sirtuin 1 (SIRT1) could play a crucially protective role in heart diseases. Recently, numerous studies have concentrated on the role of SIRT1 in DOX-induced cardiotoxicity, which might be related to the activity and deacetylation of SIRT1 downstream targets. Therefore, the aim of this review was to summarize the recent advances related to the protective effects, mechanisms, and deficiencies in clinical application of SIRT1 in DOX-induced cardiotoxicity. Also, the pharmaceutical preparations that activate SIRT1 and affect DOX-induced cardiotoxicity have been listed in this review.

Indexed as

AnimalsAntibiotics, AntineoplasticCardiotoxicityDoxorubicinHumansSignal TransductionSirtuin 1Antibiotics, AntineoplasticDoxorubicinSirtuin 1CardiotoxicityDeacetylationDoxorubicinMechanismSIRT1SIRT1 agonists

Identifiers

PMID33438055
PMCPMC11072696
OpenAlexW3121059516

What OpenQuestion 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 OpenQuestion graph.