Literature DB >> 34035068

OCaMIR-A Noninvasive, Diagnostic Signature for Early-Stage Ovarian Cancer: A Multi-cohort Retrospective and Prospective Study.

Raju Kandimalla1, Wei Wang2,3, Fan Yu4, Nianxin Zhou5, Feng Gao6, Monique Spillman7, Lucie Moukova8, Ondrej Slaby9,10, Bodour Salhia11, Shengtao Zhou12, Xin Wang13,14, Ajay Goel15,16.   

Abstract

PURPOSE: Due to the lack of effective screening approaches and early detection biomarkers, ovarian cancer has the highest mortality rates among gynecologic cancers. Herein, we undertook a systematic biomarker discovery and validation approach to identify microRNA (miRNA) biomarkers for the early detection of ovarian cancer. EXPERIMENTAL
DESIGN: During the discovery phase, we performed small RNA sequencing in stage I high-grade serous ovarian cancer (n = 31), which was subsequently validated in multiple, independent data sets (TCGA, n = 543; GSE65819, n = 87). Subsequently, we performed multivariate logistic regression-based training in a serum data set (GSE106817, n = 640), followed by its independent validation in three retrospective data sets (GSE31568, n = 85; GSE113486, n = 140; Czech Republic cohort, n = 192) and one prospective serum cohort (n = 95). In addition, we evaluated the specificity of OCaMIR, by comparing its performance in several other cancers (GSE31568 cohort, n = 369).
RESULTS: The OCaMIR demonstrated a robust diagnostic accuracy in the stage I high-grade serous ovarian cancer patients in the discovery cohort (AUC = 0.99), which was consistently reproducible in both stage I (AUC = 0.96) and all stage patients (AUC = 0.89) in the TCGA cohort. Logistic regression-based training and validation of OCaMIR achieved AUC values of 0.89 (GSE106817), 0.85 (GSE31568), 0.86 (GSE113486), and 0.82 (Czech Republic cohort) in the retrospective serum validation cohorts, as well as prospective validation cohort (AUC = 0.92). More importantly, OCaMIR demonstrated a significantly superior diagnostic performance compared with CA125 levels, even in stage I patients, and was more cost-effective, highlighting its potential role for screening and early detection of ovarian cancer.
CONCLUSIONS: Small RNA sequencing identified a robust noninvasive miRNA signature for early-stage serous ovarian cancer detection. ©2021 American Association for Cancer Research.

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Year:  2021        PMID: 34035068     DOI: 10.1158/1078-0432.CCR-21-0267

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  5 in total

Review 1.  Non-coding RNAs as liquid biopsy biomarkers in cancer.

Authors:  Shusuke Toden; Ajay Goel
Journal:  Br J Cancer       Date:  2022-01-10       Impact factor: 7.640

Review 2.  Current and Emerging Methods for Ovarian Cancer Screening and Diagnostics: A Comprehensive Review.

Authors:  Juliane M Liberto; Sheng-Yin Chen; Ie-Ming Shih; Tza-Huei Wang; Tian-Li Wang; Thomas R Pisanic
Journal:  Cancers (Basel)       Date:  2022-06-11       Impact factor: 6.575

Review 3.  Toward More Comprehensive Homologous Recombination Deficiency Assays in Ovarian Cancer, Part 1: Technical Considerations.

Authors:  Stanislas Quesada; Michel Fabbro; Jérôme Solassol
Journal:  Cancers (Basel)       Date:  2022-02-23       Impact factor: 6.639

4.  Predict ovarian cancer by pairing serum miRNAs: Construct of single sample classifiers.

Authors:  Guini Hong; Fengyuan Luo; Zhihong Chen; Liyuan Ma; Guiyang Lin; Tong Wu; Na Li; Hao Cai; Tao Hu; Haijian Zhong; You Guo; Hongdong Li
Journal:  Front Med (Lausanne)       Date:  2022-08-02

Review 5.  The Role of miRNA in Ovarian Cancer: an Overview.

Authors:  Lihui Zhao; Xiaolei Liang; Liyan Wang; Xuehong Zhang
Journal:  Reprod Sci       Date:  2022-01-01       Impact factor: 2.924

  5 in total

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