Kumar Amit, Gupta Ragni, Rashid Haroon, Bhat Aalim Maqsood, Sharma Raghu Rai, Naikoo Shahid Hussain, Kaur Sarabjit, Tasduq Sheikh Abdullah
Natural Product and Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine Jammu-180001 Jammu and Kashmir India.
Department of Pharmaceutical Sciences, Guru Nanak Dev University Amritsar-143005 India.
RSC Adv. 2023 Apr 11;13(16):11130-11141. doi: 10.1039/d2ra08023k. eCollection 2023 Apr 3.
Melanoma, the most serious yet uncommon type of cancer, originates in melanocytes. Risk factors include UV radiation, genetic factors, tanning lamps and beds. Here, we described the synthesis and selective anti melanoma activity of [3,2-]indole fused 18β-glycyrrhetinic acid, a derivative of 18β-glycyrrhetinic acid in murine B16F10 and A375 human melanoma cell lines. Among the 14 molecules, GPD-12 showed significant selective cytotoxic activity against A375 and B16F10 cell lines with IC50 of 13.38 μM and 15.20 μM respectively. GPD 12 induced the formation of reactive oxygen species in A375 cells that could trigger oxidative stress mediated cell death as is evident from the increased expression of apoptosis related proteins such as caspase-9 and caspase-3 and the increased ratio of Bax to Bcl2. The results showed that GPD 12 can be used as an effective therapeutic agent against melanoma.
黑色素瘤是最严重但并不常见的癌症类型,起源于黑素细胞。风险因素包括紫外线辐射、遗传因素、晒黑灯和晒黑床。在此,我们描述了[3,2-]吲哚稠合的18β-甘草次酸(18β-甘草次酸的一种衍生物)在小鼠B16F10和人A375黑色素瘤细胞系中的合成及选择性抗黑色素瘤活性。在这14种分子中,GPD-12对A375和B16F10细胞系表现出显著的选择性细胞毒性活性,IC50分别为13.38 μM和15.20 μM。GPD 12诱导A375细胞中活性氧的形成,这可能引发氧化应激介导的细胞死亡,这从凋亡相关蛋白如caspase-9和caspase-3的表达增加以及Bax与Bcl2的比例增加可以明显看出。结果表明,GPD 12可作为一种有效的抗黑色素瘤治疗药物。