Evidence map›Paper›PMID 35682716›Full record

ArticleInternational journal of molecular sciences2022

Expression Profiles of Circulating MicroRNAs in XELOX-Chemotherapy-Induced Peripheral Neuropathy in Patients with Advanced Gastric Cancer.

Yeongdon Ju, Young Mi Seol, Jungho Kim, Hyunwoo Jin, Go-Eun Choi, Aelee Jang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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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

6 authors at 3 institutions in 1 country.

Yeongdon JuDepartment of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea.ORCID 0000-0002-7792-1946
Young Mi SeolDivision of Hematology-Oncology, Department of Internal Medicine and Biomedical Research Institute, Pusan National University Hospital, Busan 49241, Korea.
Jungho KimDepartment of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea.
Hyunwoo JinDepartment of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea.ORCID 0000-0003-1773-023X
Go-Eun ChoiDepartment of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea.ORCID 0000-0003-0800-2919
Aelee JangDepartment of Nursing, University of Ulsan, Ulsan 44610, Korea.ORCID 0000-0002-4060-1279
Catholic University of Pusan · KRPusan National University Hospital · KRUniversity of Ulsan · KR

Funding

The National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) NRF-2019R1C1C1004820The National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) NRF-2019R1F1A1063299
6 · The paper itself

Abstract

Gastric cancer (GC) is one of the most common cancers and a leading cause of cancer deaths around the world. Chemotherapy is one of the most effective treatments for cancer patients, and has remarkably enhanced survival rates. However, it has many side effects. Recently, microRNAs (miRNAs) have been intensively studied as potential biomarkers for cancer diagnosis and treatment monitoring. However, definitive biomarkers in chemotherapy-induced peripheral neuropathy (CIPN) are still lacking. The aim of this study was to identify the factors significant for neurological adverse events in GC patients receiving XELOX (oxaliplatin and capecitabine) chemotherapy. The results show that XELOX chemotherapy induces changes in the expression of hsa-miR-200c-3p, hsa-miR-885-5p, and hsa-miR-378f. Validation by qRT-PCR demonstrated that hsa-miR-378f was significantly downregulated in CIPN. Hsa-miR-378f was identified as showing a statistically significant correlation in GC patients receiving XELOX chemotherapy according to the analysis of differentially expressed (DE) miRNAs. Furthermore, 34 potential target genes were predicted using a web-based database for miRNA target prognostication and functional annotations. The identified genes are related to the peptidyl-serine phosphorylation and regulation of alternative mRNA splicing with enrichment in the gastric cancer, neurotrophin, MAPK, and AMPK signaling pathways. Collectively, these results provide information useful for developing promising strategies for the treatment of XELOX-chemotherapy-induced peripheral neuropathy.

Indexed as

Antineoplastic AgentsCirculating MicroRNAMicroRNAsPeripheral Nervous System DiseasesStomach NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsBiomarkersCapecitabineGene Expression ProfilingHumansOxaloacetatesAntineoplastic AgentsBiomarkersCapecitabineCirculating MicroRNAMicroRNAsOxaloacetatesbioinformatics analysischemotherapy-induced peripheral neuropathygastric cancermicroRNAs

Identifiers

PMID35682716
PMCPMC9180980
OpenAlexW4281636390

What OpenQuestion holds

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LicenceCC BY
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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.