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Published on: December 13, 2018
Exosomal long non-coding RNA UCA1 functions as growth inhibitor in esophageal cancer
Zijiang Zhu1, Huilin Wang1, Yao Pang1
1Department of Thoracic Surgery, Gansu Provincial Hospital, Lanzhou, Gansu, China.
Purpose:
Esophageal cancer is a highly lethal and broad-spreading malignant tumor worldwide. Exosome-carrying lncRNAs play an essential role in the pathogenesis of various cancers.
Results:
The results revealed that the expression of UCA1 was decreased in esophageal cancer tissues and plasma exosomes. UCA1 was enriched in exosomes, and exosomal UCA1 was a promising biomarker for the diagnosis of esophageal cancer with 86.7% sensitivity and 70.2% specificity. Overexpression of UCA1 played anticancer roles in esophageal cancer cells through inhibiting cell proliferation, invasion and migration, and colony formation. Also, exosomal UCA1 was taken up by esophageal cancer cells and inhibited the progression of esophageal cancer in vitro and tumor growth in vivo. Furthermore, exosomal UCA1 could directly target miRNA-613 in esophageal cancer cells.
Conclusions:
The results suggested that exosomal UCA1 inhibits tumorigenesis and progression of esophageal cancer in vitro and in vivo, and might be a promising biomarker for esophageal cancer.
Patient And Methods:
In this study, we determined the expression of UCA1 in esophageal cancer tissues, plasma exosomes of patients with esophageal cancer. We determined the potential of exosomal UCA1 as a biomarker and its effect on the pathogenesis and progression of esophageal cancer in vitro and in vivo.
Insights
Decreased UCA1 in exosomes is linked to esophageal cancer. Exosomal UCA1 shows diagnostic potential and inhibits cancer progression, offering a new therapeutic target for this lethal disease.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Esophageal cancer is a globally prevalent and highly lethal malignancy.
- Exosome-associated long non-coding RNAs (lncRNAs) are implicated in cancer development.
Purpose of the Study:
- To investigate the expression of UCA1 in esophageal cancer.
- To evaluate exosomal UCA1 as a diagnostic biomarker.
- To determine the therapeutic potential of exosomal UCA1 in esophageal cancer.
Main Methods:
- Quantification of UCA1 expression in esophageal cancer tissues and plasma exosomes.
- Assessment of exosomal UCA1's diagnostic accuracy (sensitivity and specificity).
- In vitro and in vivo studies on the effects of UCA1 overexpression and exosomal UCA1 uptake on esophageal cancer cells and tumor growth.
Main Results:
- UCA1 expression was significantly decreased in esophageal cancer tissues and plasma exosomes.
- Exosomal UCA1 demonstrated diagnostic potential with 86.7% sensitivity and 70.2% specificity.
- Overexpression of UCA1 inhibited esophageal cancer cell proliferation, invasion, migration, and colony formation, and exosomal UCA1 targeted miRNA-613.
Conclusions:
- Exosomal UCA1 plays an inhibitory role in esophageal cancer progression both in vitro and in vivo.
- Exosomal UCA1 represents a promising biomarker for esophageal cancer diagnosis and a potential therapeutic agent.
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