新型 NF-κB 抑制剂 (S)-b-salicyloylamino-a-exo-methylene-ƴ-butyrolactone 在二维和三维乳腺癌模型中的抗移行作用。

Paola Poma, Salvatrice Rigogliuso, Manuela Labbozzetta, Francesco Carfì Pavia, Camilla Carbone, Jun Ma, Alessandra Cusimano, Monica Notarbartolo
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摘要

治疗肿瘤疾病的药理学方法之一是针对肿瘤细胞的转移能力,以减少其侵袭行为。在这项研究中,我们分析了化合物 SEMBL((S)-β-水杨酰氨基-a-外亚甲基-ƴ-丁内酯,一种 (-)-Dehydroxymethylepoxyquinomicin ((-)-DHMEQ) 的新类似物)在三种不同乳腺癌细胞系中的抗转移能力:MCF-7、MCF-7R 和 MDA-MB-231。通过 MTS 法评估,该分子具有很强的抗增殖活性,比 DHMEQ 更强。通过 TransAM™ 检测法观察到,SEMBL 能够抑制核因子κκB(NF-κB)的活化,而通过金属蛋白酶 2(MMP-2)和波形蛋白(Vimentin)的减少,细胞侵袭和伤口愈合检测显示其侵袭能力大大降低。这些在体外获得的结果在聚乳酸(PLLA)支架组成的三维系统中得到了证实。总之,SEMBL在临床前乳腺癌模型中发挥了有趣的抗肿瘤活性,因此它可能是一种很有前途的新分子,也可用于其他类型肿瘤疾病的研究。
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Antimigratory effects of a new NF-κB inhibitor, (S)-b-salicyloylamino-a-exo-methylene-ƴ-butyrolactone, in 2D and 3D breast cancer models.

One of the pharmacological approaches to neoplastic disease aims to target the metastatic capacity of tumor cells to reduce their aggressive behavior. In this study, we analyzed the antimigratory capacity of the compound SEMBL, (S)-β-salicyloylamino-a-exo-methylene-ƴ-butyrolactone, a new analog of (-)-Dehydroxymethylepoxyquinomicin ((-)-DHMEQ), in three different breast cancer cell lines: MCF-7, MCF-7R and MDA-MB-231. This molecule is characterized by intense antiproliferative activity, evaluated by MTS assay, showing greater potency than DHMEQ. SEMBL was able to inhibit nuclear factor κappa B (NF-κB) activation observed through TransAM™ assay, while cell invasion and wound healing assays revealed a strong reduction in invasive capacity mediated by metalloproteinase 2 (MMP-2) and Vimentin decrease. These results, obtained in vitro, were corroborated on 3D systems made up of Poly-L-Lactic Acid (PLLA) scaffolds. In summary, SEMBL exerts interesting anti-tumor activities in preclinical breast cancer models and therefore it could be a promising new molecule to be studied also in other types of neoplastic disease.

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