Small molecule as potent hepatocellular carcinoma progression inhibitor through stabilizing G-quadruplex DNA to activate replication stress responded DNA damage

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fei Huang , Yan Liu , Jinhua Huang , Dongqing He , Qiong Wu , Yongchang Zeng , Bin Zhao , Wenjie Mei
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引用次数: 0

Abstract

G-quadruplex (G4) DNA, prevalent in tumor cells, offers a potential anticancer target. This study examined TA-1, a tanshinone IIA derivative, for its antitumor activity against liver cancer. We found that TA-1 binds and stabilizes multiple G4 DNA,triggering DNA damage, suppressing the angiogenesis in vitro and in vivo and leading to cancer cell death. Notably, we confirmed TA-1's inhibitory effect on liver cancer cells and explored its mechanism, which involves stabilizing G4 DNA to mediate replication-stress-dependent DNA damage. Furthermore, TA-1 promotes 53BP1 expression, activating toxic NHEJ repair and leading to apoptotic cell death via the ATM-Chk2-p53 pathway. In vivo studies further supported these findings. In summary, TA-1 is a potent VEGF G-quadruplex stabilizer that inhibits liver cancer progression.

Abstract Image

小分子作为有效的肝癌进展抑制剂,通过稳定g -四重体DNA激活复制应激应答的DNA损伤。
普遍存在于肿瘤细胞中的g -四重体(G4) DNA提供了一个潜在的抗癌靶点。本研究考察了丹参酮IIA衍生物TA-1对肝癌的抗肿瘤活性。我们发现TA-1结合并稳定多个G4 DNA,引发DNA损伤,抑制体外和体内血管生成,导致癌细胞死亡。值得注意的是,我们证实了TA-1对肝癌细胞的抑制作用,并探讨了其机制,包括稳定G4 DNA介导复制应激依赖性DNA损伤。此外,TA-1通过ATM-Chk2-p53通路促进53BP1表达,激活毒性NHEJ修复并导致凋亡细胞死亡。体内研究进一步支持了这些发现。综上所述,TA-1是一种有效的抑制肝癌进展的VEGF g -四重体稳定剂。
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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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