Evidence map›Paper›PMID 37987209›Full record

ArticleCancer medicine2023

Radiotranscriptomics identified new mRNAs and miRNA markers for distinguishing prostate cancer from benign prostatic hyperplasia.

Qian Yang, Qiuyang Li, Nan Li, Dingyi Wang, Shaoxi Niu, Peng Tang, Jing Xiao, Jiahang Zhao, Pei Wang, Yukun Luo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

11 authors at 3 institutions in 2 countries.

Qian YangDepartment of Ultrasound, Air Force Medical Center, PLA, Air Force Military Medical University, Beijing, China.ORCID 0000-0003-4401-1257
Qiuyang LiDepartment of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Nan LiDepartment of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Dingyi WangDepartment of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Shaoxi NiuDepartment of Urology, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Peng TangDepartment of Orthopedics, China Rehabilitation Research Center, Beijing Charity Hospital, Beijing, China.
Jing XiaoDepartment of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Jiahang ZhaoDepartment of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Pei WangDepartment of Ultrasound Diagnosis and Treatment Center, Xi'an International Medical Center Hospital, Xian, China.
Yukun LuoDepartment of Ultrasound, Air Force Medical Center, PLA, Air Force Military Medical University, Beijing, China.
Jie TangDepartment of Ultrasound, First Medical Center, Chinese PLA General Hospital, Beijing, China.
Chinese PLA General Hospital · CNChina Rehabilitation Research Center · CNMedical Center Hospital · US

Funding

China Postdoctoral Science Foundation 2021T140795National Natural Science Foundation of China 81471682National Natural Science Foundation of China 81801708Natural Science Basic Research Program of Shaanxi Province 2023-JC-QN-0912Xi'an International Medical Center Hospital Level Project 2022QN01Xi'an Science and Technology Plan Project 21YXYJ0134
6 · The paper itself

Abstract

The present study investigated ultrasound (US) phenotypes reflecting prostate cancer (PCa)-related genetic mutations. Herein, integration of radiotranscriptomic data, US and contrast-enhanced ultrasound (CEUS) radiomic images, and RNA sequencing was performed with the aim of significantly improving the accuracy of PCa prognosis. We performed radiotranscriptomic analysis of clinical, imaging, and two genomic (mRNA and microRNA expression) datasets from 48 and 22 men with PCa and benign prostatic hyperplasia (BPH), respectively. Twenty-three US texture features and four microvascular perfusion features were associated with various patterns of 52 differentially expressed genes related to PCa (p < 0.05); 17 overexpressed genes were associated with two key texture features. Twelve overexpressed genes were identified using microvascular perfusion features. Furthermore, mRNA and miRNA biomarkers could be used to distinguish between PCa and BPH. Compared with RNA sequencing, B-mode and CEUS features reflected genomic alterations associated with hormone receptor status, angiogenesis, and prognosis in patients with PCa. These findings indicate the potential of US to assess biomarker levels in patients with PCa.

Indexed as

MicroRNAsProstatic HyperplasiaProstatic NeoplasmsBiomarkersHumansMaleRNA, MessengerBiomarkersMicroRNAsRNA, Messengerprostate cancerradiomicsradiotranscriptomicsultrasound

Identifiers

PMID37987209
PMCPMC10757143
OpenAlexW4388870290

What OpenQuestion holds

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Registered trials

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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.