Evidence map›Paper›PMID 35222406›Full record

ArticleFrontiers in immunology2022

Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib.

Ping Du, Lingling Xuan, Ting Hu, Zhuoling An, Lihong Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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 2 institutions in 1 country.

Ping DuDepartment of Pharmacy/Phase I Clinical Trial & Research Unit, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Lingling XuanDepartment of Pharmacy/Phase I Clinical Trial & Research Unit, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Ting HuDepartment of Pharmacy/Phase I Clinical Trial & Research Unit, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Zhuoling AnDepartment of Pharmacy/Phase I Clinical Trial & Research Unit, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Lihong LiuDepartment of Pharmacy/Phase I Clinical Trial & Research Unit, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Beijing Chao-Yang Hospital · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anlotinib (ANL) shows promising efficacy in patients with renal cell cancer (RCC). Here, for the first time, a serum eicosanoid metabolomics profile and pharmacodynamics in Renca syngeneic mice treated with ANL was performed and integrated using our previous HPLC-MS/MS method and multivariate statistical analysis. The tumor growth inhibition rates of ANL were 39% and 52% at low (3 mg/kg) and high (6 mg/kg) dose levels, without obvious toxicity. A total of 15 disturbed metabolites were observed between the normal group and the model group, and the intrinsic metabolic phenotype alterations had occurred due to the treatment of ANL. A total of eight potential metabolites from the refined partial least squares (PLS) model were considered as potential predictive biomarkers for the efficacy of ANL, and the DHA held the most outstanding sensitivity and specificity with an area under the receiver operating characteristic curve of 0.88. Collectively, the results of this exploratory study not only provide a powerful reference for understanding eicosanoid metabolic reprogramming of ANL but also offer an innovative perspective for the development of therapeutic targets and strategies, the discovery of predictive biomarkers, and the determination of effective tumor monitoring approaches.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAnimalsBiomarkersDisease Models, AnimalEicosanoidsHumansIndolesMetabolomicsMiceQuinolinesTandem Mass SpectrometryanlotinibBiomarkersEicosanoidsIndolesQuinolinesanlotinibeicosanoidsmetabolomicspharmacodynamicsrenal cell carcinoma

Identifiers

PMID35222406
PMCPMC8863591
OpenAlexW4211009644

What OpenQuestion holds

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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.