Evidence map›Paper›PMID 35779877›Full record

ArticleAdvances in cancer research2022

Nephrotoxicity in cancer treatment: An update.

Chaoling Chen, Dengpiao Xie, David A Gewirtz, Ningjun Li

Open access · greenAbstract read
In one paragraph

Article in Advances in cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
44.6field-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

16 citing papers in PubMed, 28 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

4 authors at 1 institution in 1 country.

Chaoling ChenDepartment of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, United States.
Dengpiao XieDepartment of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, United States.
David A GewirtzDepartment of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, United States.
Ningjun LiDepartment of Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, United States. Electronic address: ningjun.li@vcuhealth.org.
Virginia Commonwealth University · US

Funding

Renal sphingosine-1-phosphate receptor 1 in salt-sensitive hypertensionR01HL145163 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI LI, NINGJUN · 2019 to 2022
$1.6M
Molecular mechanism of hypertension-induced renal injury: the role of HIF-1alphaR01DK107991 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI LI, NINGJUN · 2017 to 2019
$698k
Inhibition of fatty acid amide hydrolase as a novel strategy to prevent nephrotoxicity of cisplatin.R21CA274012 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI LI, NINGJUN · 2022 to 2023
$398k
NCI NIH HHS R21 CA274012NHLBI NIH HHS R01 HL145163NIDDK NIH HHS R01 DK107991
6 · The paper itself

Abstract

It has been estimated that nearly 80% of anticancer drug-treated patients receive potentially nephrotoxic drugs, while the kidneys play a central role in the excretion of anticancer drugs. Nephrotoxicity has long been a serious complication that hampers the effectiveness of cancer treatment and continues to influence both mortality and length of hospitalization among cancer patients exposed to either conventional cytotoxic agents or targeted therapies. Kidney injury arising from anticancer drugs tends to be associated with preexisting comorbidities, advanced cancer stage, and the use of concomitant non-chemotherapeutic nephrotoxic drugs. Despite the prevalence and impact of kidney injury on therapeutic outcomes, the field is sorely lacking in an understanding of the mechanisms driving cancer drug-induced renal pathophysiology, resulting in quite limited and largely ineffective management of anticancer drug-induced nephrotoxicity. Consequently, there is a clear imperative for understanding the basis for nephrotoxic manifestations of anticancer agents for the successful management of kidney injury by these drugs. This article provides an overview of current preclinical research on the nephrotoxicity of cancer treatments and highlights prospective approaches to mitigate cancer therapy-related renal toxicity.

Indexed as

Antineoplastic AgentsDrug-Related Side Effects and Adverse ReactionsNeoplasmsHumansKidneyProspective StudiesAntineoplastic AgentsChemotherapyImmune checkpointKidney toxicityNon-coding RNAsRisk factorSphingolipidsTargeted cancer therapy

Identifiers

PMID35779877
PMCPMC11017963
OpenAlexW4226132839

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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.