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    標題: A fluorene derivative inhibits human hepatocellular carcinoma cells by ROS-mediated apoptosis, anoikis and autophagy
    作者: Urade, Ritesh
    Chang, Wen-Tsan
    Ko, Ching-Chung
    Li, Ruei-Nian
    Yang, Hui-Min
    Chen, Hsuan-Yu
    Huang, Lin-Ya
    Chang, Meng-Yang
    Wu, Chang-Yi
    Chiu, Chien-Chih
    貢獻者: Natl Sun Yat Sen Univ, Dept Biol Sci
    Kaohsiung Med Univ, Dept Biotechnol
    Kaohsiung Med Univ Hosp, Dept Surg, Div Gen & Digest Surg
    Kaohsiung Med Univ, Coll Med, Sch Med, Dept Surg
    Chi Mei Med Ctr, Dept Med Imaging
    Chia Nan Univ Pharm & Sci, Dept Hlth & Nutr
    Kaohsiung Med Univ, Dept Biomed Sci & Environm Biol
    Kaohsiung Med Univ, Dept Med
    Kaohsiung Med Univ, Dept Med & Appl Chem
    Natl Appl Res Labs, Natl Lab Anim Ctr
    Kaohsiung Med Univ Hosp, Dept Med Res
    Kaohsiung Med Univ, Ctr Canc Res
    關鍵字: Hepatocellular carcinoma (HCC)
    Fluorene derivative MSDF
    ROS generation
    Apoptosis
    Anoikis
    Autophagy
    Immune checkpoint proteins
    日期: 2023
    上傳時間: 2024-12-25 11:04:42 (UTC+8)
    出版者: PERGAMON-ELSEVIER SCIENCE LTD
    摘要: Fluorene was previously reported to have anticancer activity against human cancer cells. In this study, we examined the in vitro function of 9-methanesulfonylmethylene-2, 3-dimethoxy-9 H-fluorene (MSDF), a novel fluorene derivative, its anticancer potential in human hepatocellular carcinoma (HCC) cells and its underlying molecular mechanism. The disruption of cellular homeostasis caused by MSDF was found to promote reactive oxygen species (ROS) generation, leading to the activation of cellular apoptosis. As a survival strategy, cells undergo autophagy during oxidative stress. MSDF-induced apoptosis occurred through both receptor-mediated extrinsic and mitochondrial-mediated intrinsic routes. The development of acidic vesicular organelles and the accumulation of LC3-II protein suggest an increase in the autophagic process. Apoptosis was detected by double staining. The MAPK/ERK and PI3K/Akt signaling pathways were indeed suppressed during treatment. Along with elevated ROS generation and apoptosis, MSDF also caused anoikis and cell death by causing cells to lose contact with their extracellular matrix. ROS production was induced by MSDF and sustained by an NAC scav-enger. MSDF-induced apoptosis led to increased autophagy, as shown by the suppression of apoptosis by Z-VAD-FMK. However, inhibition of autophagy by inhibitor 3-MA increased MSDF-induced apoptosis. More evidence shows that MSDF downregulated the expression of immune checkpoint proteins, suggesting that MSDF could be used in the future as an adjuvant to improve the effectiveness of HCC immunotherapy. Altogether, our results highlight the potential of MSDF as a multitarget drug for the treatment of HCC.
    關聯: Life Sciences, v.329, Article 121835
    顯示於類別:[行政單位] 456

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