Oridonin Suppresses the Malignant Progression of Lung Cancer by Targeting S100A11.

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Current medicinal chemistry Pub Date : 2026-01-01 DOI:10.2174/0109298673352893241228015939
Yulin Luo, Jingjing Li, Yao Chen, Yan Huang, Qi Luo, Qiang Luo, Qingqing Huang, Gang Huang, Mingming Jin
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Abstract

Background: Lung cancer (LC) is the second most lethal cancer and efficient treatments are missing. Our understanding of the underlying pathogenic mechanisms remains limited. Oridonin is a compound extracted from the Chinese herb Rabdosia rubescens with anticancer properties. Nevertheless, its effects on LC and the underlying mechanisms remain unknown.

Methods: In the current research, A549 and Hcc1833 cells were treated with different doses of oridonin, and cell proliferation and migration were detected using CCK8, EdU, Transwell, and wound healing assays. A subcutaneous tumor and caudal vein metastasis model was generated to verify the inhibitory effects of oridonin on Hcc1833 tumor growth and metastasis in vivo. Proteomics analyses then were performed to examine the regulatory mechanism. LiP-SMap combined with microscale thermophoresis and molecular docking analyses were used to validate the relationship between oridonin and S100A11.

Results: Data showed that oridonin suppressed cell proliferation and migration depending on dose and suppressed tumor growth and invasion. LiP-SMap and molecular docking analyses confirmed that oridonin interacted with the Asn-53 residue of S100A11, which inhibited the activation of oridonin. S100A11 overexpression reversed the inhibitory effects of oridonin on cell proliferation and migration.

Conclusion: In conclusion, the data indicate that oridonin suppresses LC malignant progression by targeting S100A11.

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Oridonin通过靶向S100A11抑制肺癌恶性进展
背景:肺癌(LC)是第二大致死性癌症,缺乏有效的治疗方法。我们对潜在致病机制的了解仍然有限。冬凌草素是从中草药冬凌草中提取的具有抗癌特性的化合物。然而,其对LC的影响及其潜在机制尚不清楚。方法:本研究以不同剂量的甲草甲素处理A549和Hcc1833细胞,采用CCK8、EdU、Transwell和创面愈合法检测细胞增殖和迁移。建立皮下肿瘤及尾静脉转移模型,验证冬凌草甲素对Hcc1833肿瘤体内生长和转移的抑制作用。然后进行蛋白质组学分析以检查调节机制。利用LiP-SMap结合微尺度热泳和分子对接分析验证了冬凌草甲素与S100A11的关系。结果:冬凌草甲素对细胞增殖和迁移有不同剂量的抑制作用,抑制肿瘤的生长和侵袭。LiP-SMap和分子对接分析证实,冬凌草甲素与S100A11的Asn-53残基相互作用,抑制了冬凌草甲素的活化。S100A11过表达逆转了冬甲素对细胞增殖和迁移的抑制作用。结论:综上所述,oridonin通过靶向S100A11抑制LC恶性进展。
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来源期刊
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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