Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles

被引:10
作者
Padroni, Lisa [1 ,2 ]
De Marco, Laura [1 ,2 ]
Fiano, Valentina [3 ]
Milani, Lorenzo [4 ]
Marmiroli, Giorgia [1 ,2 ]
Giraudo, Maria Teresa [4 ]
Macciotta, Alessandra [4 ]
Ricceri, Fulvio [4 ]
Sacerdote, Carlotta [1 ,2 ]
机构
[1] Citta Salute & Sci Univ Hosp, Unit Canc Epidemiol, Via St ena 7, I-10126 Turin, Italy
[2] Ctr Canc Prevent CPO, Via St ena 7, I-10126 Turin, Italy
[3] Univ Turin, Dept Med Sci, Unit Canc Epidemiol, I-10126 Turin, Italy
[4] Univ Turin, Ctr Biostat Epidemiol & Publ Hlth C BEPH, Dept Clin & Biol Sci, I-10043 Orbassano, Italy
关键词
breast cancer; microRNA; miRNA; serum; plasma; high throughput techniques; BIOMARKER; SIGNATURE; QUALITY;
D O I
10.3390/ijms242015114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The analysis of circulating tumor cells and tumor-derived materials, such as circulating tumor DNA, circulating miRNAs (cfmiRNAs), and extracellular vehicles provides crucial information in cancer research. CfmiRNAs, a group of short noncoding regulatory RNAs, have gained attention as diagnostic and prognostic biomarkers. This review focuses on the discovery phases of cfmiRNA studies in breast cancer patients, aiming to identify altered cfmiRNA levels compared to healthy controls. A systematic literature search was conducted, resulting in 16 eligible publications. The studies included a total of 585 breast cancer cases and 496 healthy controls, with diverse sample types and different cfmiRNA assay panels. Several cfmiRNAs, including MIR16, MIR191, MIR484, MIR106a, and MIR193b, showed differential expressions between breast cancer cases and healthy controls. However, the studies had a high risk of bias and lacked standardized protocols. The findings highlight the need for robust study designs, standardized procedures, and larger sample sizes in discovery phase studies. Furthermore, the identified cfmiRNAs can serve as potential candidates for further validation studies in different populations. Improving the design and implementation of cfmiRNA research in liquid biopsies may enhance their clinical diagnostic utility in breast cancer patients.
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页数:19
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