Literature DB >> 35013528

Cell-free plasma microRNAs that identify patients with glioblastoma.

Matias A Bustos1, Negin Rahimzadeh2, Suyeon Ryu3, Rebecca Gross2, Linh T Tran3, Victor M Renteria-Lopez3, Romela I Ramos2, Amy Eisenberg4, Parvinder Hothi5, Santosh Kesari4,6, Garni Barkhoudarian4, Yuki Takasumi7, Charles Cobbs5, Daniel F Kelly4, Dave S B Hoon2,3.   

Abstract

Glioblastoma (GBM) is still one of the most commonly diagnosed advanced stage primary brain tumors. Current treatments for patients with primary GBM (pGBM) are often not effective and a significant proportion of the patients with pGBM recur. The effective treatment options for recurrent GBM (rGBM) are limited and survival outcomes are poor. This retrospective multicenter pilot study aims to determine potential cell-free microRNAs (cfmiRs) that identify patients with pGBM and rGBM tumors. 2,083 miRs were assessed using the HTG miRNA whole transcriptome assay (WTA). CfmiRs detection was compared in pre-operative plasma samples from patients with pGBM (n = 32) and rGBM (n = 13) to control plasma samples from normal healthy donors (n = 73). 265 cfmiRs were found differentially expressed in plasma samples from pGBM patients compared to normal healthy donors (FDR < 0.05). Of those 193 miRs were also detected in pGBM tumor tissues (n = 15). Additionally, we found 179 cfmiRs differentially expressed in rGBM, of which 68 cfmiRs were commonly differentially expressed in pGBM. Using Random Forest algorithm, specific cfmiR classifiers were found in the plasma of pGBM, rGBM, and both pGBM and rGBM combined. Two common cfmiR classifiers, miR-3180-3p and miR-5739, were found in all the comparisons. In receiving operating characteristic (ROC) curves analysis for rGBM miR-3180-3p showed a specificity of 87.7% and a sensitivity of 100% (AUC = 98.5%); while miR-5739 had a specificity of 79.5% and sensitivity of 92.3% (AUC = 90.2%). This study demonstrated that plasma samples from pGBM and rGBM patients have specific miR signatures. CfmiR-3180-3p and cfmiR-5739 have potential utility in diagnosing patients with pGBM and rGBM tumors using a minimally invasive blood assay.
© 2022. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

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Year:  2022        PMID: 35013528     DOI: 10.1038/s41374-021-00720-4

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  2 in total

1.  Silencing of vacuolar ATPase c subunit ATP6V0C inhibits the invasion of prostate cancer cells through a LASS2/TMSG1-independent manner.

Authors:  Pengcheng Zou; Yifeng Yang; Xiaoyan Xu; Beiying Liu; Fang Mei; Jiangfeng You; Qichen Liu; Fei Pei
Journal:  Oncol Rep       Date:  2017-11-10       Impact factor: 3.906

Review 2.  Liquid biopsy in central nervous system tumors: the potential roles of circulating miRNA and exosomes.

Authors:  Yirizhati Aili; Nuersimanguli Maimaitiming; Yusufu Mahemuti; Hu Qin; Yongxin Wang; Zengliang Wang
Journal:  Am J Cancer Res       Date:  2020-12-01       Impact factor: 6.166

  2 in total
  1 in total

1.  Urine Cell-Free MicroRNAs in Localized Prostate Cancer Patients.

Authors:  Yoko Koh; Matias A Bustos; Jamie Moon; Rebecca Gross; Romela Irene Ramos; Suyeon Ryu; Jane Choe; Selena Y Lin; Warren M Allen; David L Krasne; Timothy G Wilson; Dave S B Hoon
Journal:  Cancers (Basel)       Date:  2022-05-12       Impact factor: 6.575

  1 in total

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