ADAR2-mediated A-to-I editing confers an oncogenic role on miR-376a-3p by shifting its target from KPNA4 to HOXD10, thereby facilitating PTC tumorigenesis through enhanced glycolysis.
It is suggested that lnc-DNAJC3-AS1 promotes GC progression, at least in part, through the miR-576-5p/LYPLA1 pathway, providing a potential target for GC treatment.
Zhen-Ni Sun, Ya-Sai Yao, Zhi-Jian Xu et al.· American Journal of Cancer R...· 0 citations
Within the present study, the objective was to investigate the effects of exosomal miR-145-5p on the proliferation, migration and invasion of papillary thyroid cancer (PTC) cells, and explore the molecular mechanism involved. Bioinformatics analyses based on numerous public databases were conducted to profile the expre...
Yun-Feng Weng, Xian-Jiao Cao, Wen-Yan Song et al.· Oncology Letters· 0 citations
Hepatocellular carcinoma (HCC) remains one of the most prevalent and lethal malignancies worldwide, characterized by limited treatment options and a poor prognosis. Emerging evidence underscores the central role of metabolic reprogramming in HCC development, with microRNAs (miRNAs) recognized as key modulators. However...
It is argued that while epitranscriptomics represents a compelling regulatory axis in cancer cell death, advancing the field will require integrative, high-resolution, and functionally precise approaches to move beyond correlative frameworks toward mechanistic and clinically actionable insights.
A. Mukherjee, Ankit Kumar Bharti, D. Mathew et al.· Functional & Integrative Gen...· 0 citations
Mechanistic studies demonstrated that circ_ATP5A1 acts as a ceRNA by sponging hsa-miR-145-5p, thereby relieving the repressive effect of hsa-miR-145-5p on its downstream target ZFP36.
Peng Huang, Ling-Zhang Meng, Jing Ma et al.· Hereditas· 0 citations
Evidence is provided for a novel UCA1 interaction regulatory network in bladder cancer, that is, UCA1-miR-582-5p-ATG7-autophagy axis, which provides a new insight into the treatment of bladder cancer.
Jun-Feng Wu, Wei Li, Jin-Zhuo Ning et al.· 0 citations