Expression of Circulating MicroRNA-141 in Epithelial Ovarian Cancer
Epithelial ovarian cancer (EOC) is a lethal disease due to late diagnosis and lack of effective screening methods. MicroRNA (miR/miRNA) plays an important role in ovarian carcinogenesis and may serve as a non-invasive biomarker for EOC. This study aimed to assess miR-141 expression in the blood plas...
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Published in | The Malaysian journal of medical sciences Vol. 27; no. 6; pp. 27 - 38 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Malaysia
Universiti Sains Malaysia Press
01.12.2020
Penerbit Universiti Sains Malaysia |
Subjects | |
Online Access | Get full text |
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Summary: | Epithelial ovarian cancer (EOC) is a lethal disease due to late diagnosis and lack of effective screening methods. MicroRNA (miR/miRNA) plays an important role in ovarian carcinogenesis and may serve as a non-invasive biomarker for EOC. This study aimed to assess miR-141 expression in the blood plasma of patients with EOC and healthy subjects and determine its association with the clinical stage of EOC.
This cross-sectional study used blood plasma from 30 newly diagnosed untreated patients with EOC and 25 healthy subjects. The mean age was 47.73 (SD = 10.29) years for EOC and 44.48 (SD = 16.14) years for healthy subject. The total RNA was isolated from blood plasma and reversed transcribed to obtain cDNA. The expression of miR-141 was measured by real-time quantitative polymerase chain reaction (qRT-PCR), and calculated using 2
methods. The data were analysed using Mann-Whitney test.
The expression of miR-141 was upregulated 8.41 fold in the blood plasma of EOC patients compared to healthy controls (
< 0.001). Expression of miR-141 in the advanced stage was upregulated 4.2 fold compared to the early stage (
< 0.001).
The miR-141 was upregulated in the blood plasma of EOC and associated with an advanced stage of disease, suggesting it has potential as a biomarker for EOC detection. |
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ISSN: | 1394-195X 2180-4303 |
DOI: | 10.21315/mjms2020.27.6.4 |