Zhang Hao, Zhao Ying, Chen Tingting, Mao Xinliang, Li Jiping, Fan Li, Li Min, Wen Xianchun
Pharmacy School, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Medical Technology School, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Front Oncol. 2025 May 27;15:1573628. doi: 10.3389/fonc.2025.1573628. eCollection 2025.
Melanoma is the most aggressive skin tumor, and conventional treatment is ineffective. Studies have shown that shikonin, derived from the traditional Chinese medicine , has various anticancer activities. In this work, RGD- modified liposomes encapsulated with shikonin (RGD-Lip-SHK) were prepared by thin- film dispersion, which could highly recognize the integrin αβ on the surface of melanoma cells. RGD-Lip-SHK appeared as spheroid-like vesicles with a particle size of approximately 120 nm, and its ξ-potential was negative. RGD-Lip-SHK remained stable in serum within 48 h and possessed sustained-release effect. , compared with non -targeted liposomes (Lip-SHK), RGD-Lip-SHK was more efficiently taken up, had higher cytotoxicity, was better targeted to inhibit cell growth, migration, and invasion, and boost cell apoptosis by regulating the expression of Bcl-2 and Bax proteins in melanoma cells. , RGD-Lip-SHK had the strongest targeted anti-melanoma effect by αβ-mediated endocytosis with a long circulation time and inhibited tumor growth in B16F10 tumor-bearing mice compared to other groups. Furthermore, the histology of major organs and the body weight of mice showed that RGD-Lip-SHK had less toxicity. In summary, these results indicated that RGD-Lip-SHK has great potential for the targeted treatment of melanoma, and is expected to become a novel and highly effective strategy for tumor-targeted therapy.
黑色素瘤是最具侵袭性的皮肤肿瘤,传统治疗方法无效。研究表明,源自中药的紫草素具有多种抗癌活性。在本研究中,采用薄膜分散法制备了包裹紫草素的RGD修饰脂质体(RGD-Lip-SHK),其能够高度识别黑色素瘤细胞表面的整合素αβ。RGD-Lip-SHK呈类球状囊泡,粒径约为120nm,其ξ电位为负。RGD-Lip-SHK在血清中48小时内保持稳定并具有缓释效果。与非靶向脂质体(Lip-SHK)相比,RGD-Lip-SHK的摄取效率更高,具有更高的细胞毒性,能更好地靶向抑制细胞生长、迁移和侵袭,并通过调节黑色素瘤细胞中Bcl-2和Bax蛋白的表达促进细胞凋亡。通过αβ介导的内吞作用,RGD-Lip-SHK具有最强的靶向抗黑色素瘤作用,循环时间长,与其他组相比,可抑制B16F10荷瘤小鼠的肿瘤生长。此外,主要器官的组织学检查和小鼠体重表明,RGD-Lip-SHK的毒性较小。综上所述,这些结果表明RGD-Lip-SHK在黑色素瘤的靶向治疗方面具有巨大潜力,有望成为肿瘤靶向治疗的一种新型高效策略。