Evidence map›Paper›PMID 35028969›Full record

ArticleJournal of clinical laboratory analysis2022

A panel of three serum microRNA can be used as potential diagnostic biomarkers for nasopharyngeal carcinoma.

Rongkang Li, Chong Lu, Weiqiang Yang, Yaqi Zhou, Jiatao Zhong, Xuan Chen, Xinji Li, Guocheng Huang, Xiqi Peng, Kaihao Liu and 3 more

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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

13 authors.

Rongkang LiDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Chong LuDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Weiqiang YangDepartment of Otorhinolaryngology, Peking University Shenzhen Hospital, Shenzhen, China.
Yaqi ZhouDepartment of Otorhinolaryngology, Peking University Shenzhen Hospital, Shenzhen, China.
Jiatao ZhongDepartment of Otorhinolaryngology, Peking University Shenzhen Hospital, Shenzhen, China.
Xuan ChenDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Xinji LiDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Guocheng HuangDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Xiqi PengDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Kaihao LiuDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Chunduo ZhangDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Hongyi HuDepartment of Otorhinolaryngology, Peking University Shenzhen Hospital, Shenzhen, China.
Yongqing LaiDepartment of Urology, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.ORCID https://orcid.org/0000-0002-5353-9355

Funding

Clinical Research Project of Peking University Shenzhen Hospital LCYJ2017001Clinical Research Project of Shenzhen Health Commission SZLY2018023Science and Technology Development Fund Project of Shenzhen JCYJ20180507183102747Shenzhen High-level Hospital Construction Fund, Basic Research Project of Peking University Shenzhen Hospital JCYJ2017001Shenzhen High-level Hospital Construction Fund, Basic Research Project of Peking University Shenzhen Hospital JCYJ2017004Shenzhen High-level Hospital Construction Fund, Basic Research Project of Peking University Shenzhen Hospital JCYJ2017005Shenzhen High-level Hospital Construction Fund, Basic Research Project of Peking University Shenzhen Hospital JCYJ2017006Shenzhen High-level Hospital Construction Fund, Basic Research Project of Peking University Shenzhen Hospital JCYJ2017007Shenzhen High-level Hospital Construction Fund, Basic Research Project of Peking University Shenzhen Hospital JCYJ2017012
6 · The paper itself

Abstract

backgroundNasopharyngeal carcinoma is cancer with unique epidemiological characteristics, showing obvious ethnicity, gender, and geographical prevalence. More and more evidence shows that microRNAs are stable in serum and are specific to different tumor types. Therefore, miRNA is a new non-invasive biomarker for cancer detection.

methodsThe experiment is divided into three stages, namely, the screening stage, the training stage, and the verification stage. We took 54 patients with nasopharyngeal carcinoma and 108 healthy controls as the research objects. We use the receiver-operating characteristic (ROC) curve and area under the ROC curve (AUC) to evaluate the diagnostic value of miRNA. Finally, a three-miRNA panel with high diagnostic efficiency was constructed. In addition, we conducted biological information analysis of these miRNAs to explore their functions.

resultsIn NPC patients, the expression of five serum miRNAs (miR-29c-3p, miR-143-5p, miR-150-5p, miR-145-3p, and miR-205-5p) is significantly dysregulated. Among them, the diagnostic value of these three miRNAs (miR-29c-3p, AUC = 0.702; miR-143-5p, AUC = 0.733; and miR-205-5p, AUC = 787) is more prominent. The diagnostic panel constructed by them has a higher diagnostic value (AUC = 0.902). Through the analysis of the TCGA data set, the target gene of the three-miRNA panel may be KLF7, NRG1, SH3BGRL2, and SYNPO2.

conclusionThe three-miRNA panel (miR-29c-3p, miR-143-5p, and miR-205-5p) may become a novel non-invasive biological marker for nasopharyngeal cancer screening.

Indexed as

AdultBiomarkers, TumorCirculating MicroRNAEarly Detection of CancerFemaleGene Expression ProfilingHumansMaleMiddle AgedNasopharyngeal CarcinomaROC CurveSensitivity and SpecificityBiomarkers, TumorCirculating MicroRNAbiomarkersmicroRNAnasopharyngeal carcinoma

Identifiers

PMID35028969
PMCPMC8842135

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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.