MedElevator Войти в исследования
← Поиск публикаций

DOI 10.2217/fon-2021-0271

Медицинская библиотека · Future oncology (London, England) · 2022

UCK2 regulated by miR-139-3p regulates the progression of hepatocellular carcinoma cells.

Yu Youlin, You Shuqing, Fan Rengen, Shan Xiangxiang

СтатьяПеревод в очереди

Аннотация

Objective

This study mainly explores how UCK2 impacts the progression of hepatocellular carcinoma (HCC).

Methods

Mature miRNA and mRNA expression data along with the clinical data of HCC were provided by The Cancer Genome Atlas to mine differentially expressed miRNAs and mRNAs. Expression levels of UCK2 and miR-139-3p in HCC were tested through quantitative real-time PCR. How UCK2 and miR-139-3p impacted HCC cell activities were detected by Transwell, wound healing and cell proliferation approaches. Whether miR-139-3p could bind to UCK2 was detected by dual-luciferase assay.

Results

This investigation found evidently high levels of UCK2 in both HCC tissue and cells and its marked association with poor prognosis. Overexpression of UCK2 could significantly promote the behaviors of HCC cells. In addition, poorly expressed miR-139-3p was inversely associated with UCK2. Dual-luciferase method also proved the association. The rescue experiment showed that miR-139-3p regulated cell behaviors in HCC through targeting UCK2.

Conclusion

Highly expressed UCK2 was mediated by miR-139-3p to modulate cell behaviors in HCC. It is assumed that UCK2 is a possible target of HCC for cancer therapy purposes.

Для цитирования: Yu Youlin, You Shuqing, Fan Rengen, Shan Xiangxiang. UCK2 regulated by miR-139-3p regulates the progression of hepatocellular carcinoma cells.. Future oncology (London, England). 2022. DOI: 10.2217/fon-2021-0271.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.