透明质酸
衰老
脂质体
化学
活力测定
细胞
肝细胞癌
细胞培养
细胞生长
癌症研究
肝癌
癌症
癌细胞
细胞毒性
药理学
药品
细胞生物学
生物化学
细胞衰老
DNA损伤
癌
癌症治疗
药物发现
癌细胞系
G2水电站
癌症治疗
DNA合成
肝癌
细胞生理学
细胞疗法
WI-38
体外
DNA
毒品携带者
细胞周期
肿瘤细胞
体内
生物
药物输送
生物活性
作者
Ruilin Lu,Xin Long,Xi‐Yao Li,Jiayan Li,Zhen Liu,Kexin Chai,Yujie Zhang,Yan Lin,Zhongbing Liu,Singkome Tima,Zhirong Zhong,Xiaoduan Sun
摘要
ABSTRACT Icaritin (ICT) shows great potential in cancer therapy. To enhance the cancer‐fighting properties of icaritin against hepatocellular carcinoma (HCC), we developed icaritin‐loaded liposomes modified with hyaluronic acid (HA‐Lip‐ICT). We employed statistical design methods to analyze how various factors affected particle dimensions and drug encapsulation, creating an optimized HA‐Lip‐ICT formulation that could effectively suppress HCC cell growth and trigger cellular aging. The human HCC cell line Huh7 was then exposed to different icaritin preparations. We assessed tumor cell viability through multiple assays, including colony formation and DNA synthesis measurements. Our results demonstrated that the refined HA‐Lip‐ICT significantly impaired HCC cell proliferation. Moreover, at a concentration of 10 μmol/L, HA‐Lip‐ICT markedly accelerated cellular senescence in HCC cells. These observations support our initial hypothesis that HA‐Lip‐ICT can inhibit HCC cell growth and promote their aging. While further research is needed to elucidate the exact mechanisms, this approach shows the promise of HA‐Lip‐ICT as a targeted therapy for improving the HCC treatments.
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