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MicroRNA Expression in Plasma of Esophageal Squamous Cell Carcinoma Patients. | LitMetric

AI Article Synopsis

  • Patients with esophageal squamous cell carcinoma (ESCC) often have a poor prognosis, and current clinical biomarkers are ineffective, prompting the investigation of blood-based microRNAs as potential biomarkers.
  • A study analyzed plasma samples from 66 ESCC patients and 16 healthy controls, measuring levels of four specific microRNAs using advanced techniques.
  • Results showed that plasma miR-21 was significantly higher, while miR-31 and miR-375 were lower in ESCC patients; notably, miR-31 and miR-375 exhibited high sensitivity and specificity for distinguishing ESCC from healthy individuals, suggesting their potential as reliable diagnostic biomarkers.

Article Abstract

Background: Patients with esophageal squamous cell carcinoma (ESCC) have a poor prognosis and there are no effective clinical biomarkers. Recently, stable microRNAs detected in the blood have been suggested as potential biomarkers in various cancers. Therefore, we investigated whether plasma microRNAs could be feasible biomarkers for ESCC.

Methods: Peripheral blood samples were obtained from 16 healthy volunteers and 66 ESCC patients before treatment between May 2016 and April 2021. Plasma miR-18b, miR-21, miR-31, and miR-375 expression levels were measured using reverse transcription-quantitative polymerase chain reaction.

Results: Compared with those in healthy controls, the expression levels of plasma miR-21 were significantly higher ( = 0.022) and those of plasma miR-31 and miR-375 were significantly lower in ESCC patients (both < 0.001). Plasma miR-18b expression levels increased in ESCC patients, but the difference was not significant ( = 0.164). The sensitivities and specificities of miR-21, miR-31, and miR-375 for differentiating ESCC patients from healthy controls were 87.5% and 61.9%, 87.5% and 98.4%, and 87.5% and 100%, respectively. There was no difference in expression levels of plasma miR-21, miR-31, and miR-375 according to clinicopathological characteristics of sex, age, tumor size and location, histologic grade, and tumor-node-metastasis stage.

Conclusion: Our study demonstrated that plasma miR-21, miR-31, and miR-375 could be potential biomarkers for the diagnosis of ESCC. Particularly, plasma miR-31 and miR-375 showed high sensitivity and specificity for differentiating ESCC patients from healthy controls.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9247724PMC
http://dx.doi.org/10.3346/jkms.2022.37.e197DOI Listing

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