Evidence map›Paper›PMID 33490068›Full record

ArticleFrontiers in cell and developmental biology2020

The Identification of Plasma Exosomal miR-423-3p as a Potential Predictive Biomarker for Prostate Cancer Castration-Resistance Development by Plasma Exosomal miRNA Sequencing.

Tianyu Guo, Yang Wang, Jing Jia, Xueying Mao, Elzbieta Stankiewicz, Glenda Scandura, Edwina Burke, Lei Xu, Jacek Marzec, Caitlin R Davies and 17 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 3 pooled it
7.9field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 3 syntheses or guidelines pooled it, 63 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

27 authors at 11 institutions in 4 countries.

Tianyu GuoCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Yang WangCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Jing JiaDepartment of Tumor Biology, H. Lee Moffitt Cancer Center, Tampa, FL, United States.
Xueying MaoCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Elzbieta StankiewiczCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Glenda ScanduraCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Edwina BurkeCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Lei XuCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Jacek MarzecCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Caitlin R DaviesCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Jiaying Jasmin LuCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Prabhakar RajanCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Alistair GreyDepartment of Urology, Barts Health NHS, London, United Kingdom.
Karen TipplesDepartment of Urology, Barts Health NHS, London, United Kingdom.
John HinesDepartment of Urology, Barts Health NHS, London, United Kingdom.
Sakunthala KudahettiCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Tim OliverCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Thomas PowlesCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Constantine AlifrangisDepartment of Urology, Barts Health NHS, London, United Kingdom.
Manish KohliDepartment of Medicine, University of Utah, Huntsman Cancer Institute, Salt Lake City, UT, United States.
Greg ShawDepartment of Urology, Barts Health NHS, London, United Kingdom.
Wen WangDivision of Bioengineering, School of Engineering and Materials Science, Queen Mary University of London, London, United Kingdom.
Ninghan FengDepartment of Urology, Affiliated Wuxi No. 2 Hospital of Nanjing Medical University, Wuxi, China.
Jonathan ShamashDepartment of Medical Oncology, Barts Health NHS, London, United Kingdom.
Daniel BerneyCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Liang WangDepartment of Tumor Biology, H. Lee Moffitt Cancer Center, Tampa, FL, United States.
Yong-Jie LuCentre for Cancer Biomarker and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Queen Mary University of London · GBBarts Health NHS Trust · GBMoffitt Cancer Center · USNanjing Medical University · CNUniversity College London · GBUniversity College London Hospitals NHS Foundation Trust · GBHuntsman Cancer Institute · USSecond Affiliated Hospital of Zhejiang University · CNSun Yat-sen University · CNUniversity of Melbourne · AUWuxi No.2 People's Hospital · CN

Funding

Cell free nucleic acid-based biomarkers in advanced prostate cancerR01CA212097 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI KOHLI, MANISH, WANG, LIANG · 2017 to 2022
$3.1M
NCI NIH HHS R01 CA212097
6 · The paper itself

Abstract

Castration-resistant prostate cancer (CRPC) is the major cause of death from prostate cancer. Biomarkers to improve early detection and prediction of CRPC especially using non-invasive liquid biopsies could improve outcomes. Therefore, we investigated the plasma exosomal miRNAs associated with CRPC and their potential for development into non-invasive early detection biomarkers for resistance to treatment. RNA-sequencing, which generated approximately five million reads per patient, was performed to identify differentially expressed plasma exosomal miRNAs in 24 treatment-naive prostate cancer and 24 CRPC patients. RT-qPCR was used to confirm the differential expressions of six exosomal miRNAs, miR-423-3p, miR-320a, miR-99a-5p, miR-320d, miR-320b, and miR-150-5p (

Indexed as

biomarkercastration-resistance developmentmiR-423-3pplasma exosome miRNAprostate cancer

Identifiers

PMID33490068
PMCPMC7817948
OpenAlexW3120465538

What OpenQuestion holds

Textmetadata
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.