共 5 条
High-throughput quantitative detection of triple-negative breast cancer-associated expressed miRNAs by rolling circle amplification on fluorescence-encoded microspheres
被引:46
|作者:
Liu, Jieyu
[1
]
Zhang, Liming
[1
]
Zeng, Wentao
[1
]
Zhang, Lihua
[2
]
He, Nongyue
[3
,4
]
Lu, Zhuoxuan
[1
]
机构:
[1] Hainan Med Univ, Sch Trop Med, Sch Basic Med & Life Sci, Micronano Technol Res Inst,Key Lab Trop Translat M, Haikou 571199, Peoples R China
[2] Beadstar Biotechnol Hainan Prov Co Ltd, Haikou 570110, Peoples R China
[3] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[4] Hunan Univ Technol, Econ Forest Cultivat & Utilizat Collaborat Innovat, Hunan Key Lab Biomed Nanomat & Devices, Zhuzhou 412007, Peoples R China
基金:
海南省自然科学基金;
关键词:
MicroRNAs;
Rolling circle amplification;
Fluorescence -encoded microspheres;
High;
-throughput;
Triple -negative breast cancer;
SUSPENSION ARRAY;
QUANTIFICATION;
MICRORNA;
FEATURES;
D O I:
10.1016/j.cclet.2023.108141
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Compared with other types of breast cancer, triple-negative breast cancer (TNBC) has the characteristics of a high degree of malignancy and poor prognosis. Early diagnosis of TNBC through biological markers and timely development of effective treatment methods can reduce its mortality. Many Research experiments have confirmed that some specific miRNA expression profiles in TNBC can used as markers for early diagnosis. However, detecting the expression profiles of multiple groups of miRNAs according to traditional detection methods is complicated and consumes many samples. To address this issue, we developed a method for high-throughput, high-sensitivity quantitative detection of multiple sets of miRNAs (including miR-16, miR-21, miR-92, miR-199, and miR-342) specifically expressed in TNBC by rolling circle amplification (RCA) on fluorescence-encoded microspheres. Through the optimization of reaction system conditions, the developed method showed an extensive linear dynamic range and high sensitivity for all five miRNAs with the lowest limit of detection of 2 fmol/L. Meanwhile, this high-throughput detection method also appeared reasonable specificity. Only in the presence of a specific target miRNA, the fluorescence signal on the correspondingly encoded microspheres is significantly increased, while the fluorescence signal on other non-correspondingly encoded microspheres is almost negligible. Furthermore, this process exhibited good recovery and reproducibility in serum. The advantages of this method allow us to more conveniently obtain the expression profiles of multiple groups of TNBC-associated miRNAs, which is beneficial for the early detection of TNBC.& COPY; 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
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