Liao Hongye, Xia Tong, Zeng Ziyuan, Yang Xun, Yang Simei, Xiong Xia, He Yuanmin, Sun Changzhen, Hao Na, Liu Li
Department of Dermatology, The Affiliated Hospital, Southwest Medical University, Luzhou, 646000, China.
School of Public Health, Southwest Medical University, Luzhou, 646000, China.
Mol Med. 2025 Jun 10;31(1):226. doi: 10.1186/s10020-025-01289-0.
Melanoma is a highly invasive and metastatic skin cancer lacking effective options for early diagnosis and treatment. To address these challenges, this study aimed to synthesize a novel near-infrared fluorescent probe and research the antitumor mechanism of melanoma.
We have designed and synthesized a novel near-infrared fluorescent probe, IR-546. This study explores imaging capabilities, anti-tumor effects, and underlying mechanisms of IR-546 in melanoma xenograft models.
In vitro, IR-546 selectively accumulates in melanoma cells, demonstrating robust tumor imaging and potent cytotoxicity by targeting mitochondria, generating reactive oxygen species (ROS), and disrupting mitochondrial membrane potential, activating the mitochondrial apoptotic pathway. Additionally, IR-546 exhibits anti-metastatic properties in vitro. In vivo, using A375 cell line-derived melanoma xenograft models, IR-546 showed significant anti-tumor effect and biosafety. Western blot analyses of both in vivo and in vitro revealed that IR-546 induces apoptosis and inhibits metastasis of melanoma by activating the mitochondrial apoptosis pathway, suppressing the AKT/GSK3β signaling pathway, and downregulating the β-catenin signaling pathway and its downstream targets. Immunohistochemistry and immunofluorescence further confirmed that IR-546 suppressed the expression of key proteins in the AKT/GSK3β pathway in vivo.
Collectively, these findings highlight IR-546 as a promising tool for both imaging and treatment of melanoma, with the potential to induce apoptosis and inhibit metastasis of melanoma through modulation of the AKT/GSK3β pathway.
Summary of the diagnostic and anti-tumor effects of IR-546 in melanoma. [Image: see text]
The online version contains supplementary material available at 10.1186/s10020-025-01289-0.
黑色素瘤是一种具有高度侵袭性和转移性的皮肤癌,缺乏早期诊断和治疗的有效方法。为应对这些挑战,本研究旨在合成一种新型近红外荧光探针,并研究黑色素瘤的抗肿瘤机制。
我们设计并合成了一种新型近红外荧光探针IR-546。本研究探讨了IR-546在黑色素瘤异种移植模型中的成像能力、抗肿瘤作用及潜在机制。
在体外,IR-546选择性地积聚在黑色素瘤细胞中,通过靶向线粒体、产生活性氧(ROS)、破坏线粒体膜电位、激活线粒体凋亡途径,显示出强大的肿瘤成像能力和强大的细胞毒性。此外,IR-546在体外具有抗转移特性。在体内,使用A375细胞系来源的黑色素瘤异种移植模型,IR-546显示出显著的抗肿瘤作用和生物安全性。体内和体外的蛋白质印迹分析表明,IR-546通过激活线粒体凋亡途径、抑制AKT/GSK3β信号通路以及下调β-连环蛋白信号通路及其下游靶点,诱导黑色素瘤细胞凋亡并抑制其转移。免疫组织化学和免疫荧光进一步证实,IR-546在体内抑制了AKT/GSK3β通路中关键蛋白的表达。
总体而言,这些发现突出了IR-546作为一种有前景的黑色素瘤成像和治疗工具的潜力,它有可能通过调节AKT/GSK3β通路诱导黑色素瘤细胞凋亡并抑制其转移。
IR-546在黑色素瘤中的诊断和抗肿瘤作用总结。[图像:见正文]
在线版本包含可在10.1186/s10020-025-01289-0获取的补充材料。