Joint International Research Laboratory of Translational Cancer Research of Chinese Medicines of the Ministry of Education of the People's Republic of China, Guangdong Provincial Key Laboratory of Translational Cancer Research of Chinese Medicines, International Institute for Translational Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Molecules. 2024 Feb 19;29(4):906. doi: 10.3390/molecules29040906.
Melanoma is the most aggressive and difficult to treat of all skin cancers. Despite advances in the treatment of melanoma, the prognosis for melanoma patients remains poor, and the recurrence rate remains high. There is substantial evidence that Chinese herbals effectively prevent and treat melanoma. The bioactive ingredient Salvianolic acid B (SAB) found in , a well-known Chinese herbal with various biological functions, exhibits inhibitory activity against various cancers. A375 and mouse B16 cell lines were used to evaluate the main targets and mechanisms of SAB in inhibiting melanoma migration. Online bioinformatics analysis, Western blotting, immunofluorescence, molecular fishing, dot blot, and molecular docking assays were carried out to clarify the potential molecular mechanism. We found that SAB prevents the migration and invasion of melanoma cells by inhibiting the epithelial-mesenchymal transition (EMT) process of melanoma cells. As well as interacting directly with the N-terminal domain of β-actin, SAB enhanced its compactness and stability, thereby inhibiting the migration of cells. Taken together, SAB could significantly suppress the migration of melanoma cells via direct binding with β-actin, suggesting that SAB could be a helpful supplement that may enhance chemotherapeutic outcomes and benefit melanoma patients.
黑色素瘤是所有皮肤癌中最具侵袭性和最难治疗的一种。尽管在治疗黑色素瘤方面取得了进展,但黑色素瘤患者的预后仍然不佳,复发率仍然很高。有大量证据表明中草药能有效预防和治疗黑色素瘤。丹参中的生物活性成分丹酚酸 B(SAB)具有多种生物学功能,对各种癌症具有抑制活性。我们使用 A375 和小鼠 B16 细胞系来评估 SAB 抑制黑色素瘤迁移的主要靶点和机制。通过在线生物信息学分析、Western blot、免疫荧光、分子捕捞、点印迹和分子对接实验,阐明了其潜在的分子机制。我们发现 SAB 通过抑制黑色素瘤细胞的上皮-间充质转化(EMT)过程来阻止黑色素瘤细胞的迁移和侵袭。SAB 直接与β-actin 的 N 端结构域相互作用,增强了其致密性和稳定性,从而抑制了细胞的迁移。总之,SAB 可以通过与β-actin 的直接结合显著抑制黑色素瘤细胞的迁移,这表明 SAB 可能是一种有益的补充,有助于增强化疗效果,使黑色素瘤患者受益。