Institute of Biomedical Chemistry, 10 Building 8, Pogodinskaya Str., 119121 Moscow, Russia.
Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, Kuprevich Str., 5/2, 220084 Minsk, Belarus.
Molecules. 2024 Aug 26;29(17):4026. doi: 10.3390/molecules29174026.
Activation of the Hedgehog (Hh) signaling pathway is often associated with the progression of various types of cancer. The purpose of study was to search for inhibitors of the Hh signaling pathway among eight compounds belonging to the group of isoxazolyl steroids. The evaluation of the effectiveness of the compounds was based on the analysis of their cytotoxicity, effect on the cell cycle, on the expression of key Hh-signaling-pathway genes (Ptch1, Smo, and Gli1) and putative target genes MMP-2 and MMP-9. Four compounds with the most pronounced cytotoxic effect were identified: compounds , (HeLa cells) and , (A549 cells). Compounds and significantly reduced the expression of the Ptch1, Smo, Gli1 genes, but had the opposite effect on MMP-2 gene expression: Compound increased it, and compound decreased it. Compounds and did not have a noticeable inhibitory effect on the expression of the Shh pathway receptors, but significantly inhibited MMP-2 and MMP-9 expression. Thus, it was shown that inhibition of the Shh signaling pathway by isoxazolyl steroids can have the opposite effect on MMPs gene expression, which is what should be taken into account in further studies of these compounds as therapeutic agents.
Hedgehog (Hh) 信号通路的激活通常与各种类型癌症的进展有关。本研究的目的是在属于异噁唑甾体类的 8 种化合物中寻找 Hh 信号通路的抑制剂。化合物有效性的评估基于对其细胞毒性、对细胞周期的影响、对关键 Hh 信号通路基因 (Ptch1、Smo 和 Gli1) 和假定靶基因 MMP-2 和 MMP-9 的表达的分析。确定了四种具有最明显细胞毒性作用的化合物:化合物 、 、 和 (HeLa 细胞)和 、 (A549 细胞)。化合物 和 显著降低了 Ptch1、Smo、Gli1 基因的表达,但对 MMP-2 基因表达有相反的影响:化合物 增加了它,而化合物 降低了它。化合物 和 对 Shh 通路受体的表达没有明显的抑制作用,但显著抑制了 MMP-2 和 MMP-9 的表达。因此,结果表明,异噁唑甾体对 Hh 信号通路的抑制作用可能对 MMPs 基因表达产生相反的影响,这在进一步研究这些化合物作为治疗剂时应予以考虑。