PTEN公司
竞争性内源性RNA
核糖核酸
小RNA
前列腺癌
癌症研究
基因表达
长非编码RNA
生物
基因
化学
癌症
生物化学
细胞凋亡
遗传学
PI3K/AKT/mTOR通路
作者
Shunye Su,Leyi Liu,Qingfeng Fu,Minghao Ma,Na Yang,Ting Pan,Shengyong Geng,Xue‐Feng Yu,Jianqiang Zhu
标识
DOI:10.1186/s12951-024-02659-2
摘要
Prostate cancer (PCa) has a high incidence in men worldwide, and almost all PCa patients progress to the androgen-independent stage which lacks effective treatment measures. PTENP1, a long non-coding RNA, has been shown to suppress tumor growth through the rescuing of PTEN expression via a competitive endogenous RNA (ceRNA) mechanism. However, PTENP1 was limited to be applied in the treatment of PCa for the reason of rapid enzymatic degradation, poor intracellular uptake, and excessively long base sequence to be synthesized. Considering the unique advantages of artificial nanomaterials in drug loading and transport, black phosphorus (BP) nanosheet was employed as a gene-drug carrier in this study.
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