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In vitro Evaluation of Anticancer Effect and Neurotoxicity of Styrylpyrone Derivative (SPD)

机译:体外评价抗癌效应和甾酮衍生物(SPD)的神经毒性

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The increasing number of death due to cancer emphasizes the need of novel anticancer agents. Styrylpyrone derivative (SPD) was previously found to have potential anticancer action towards many types of cancer. Some of the SPD-anticancer mechanisms were elucidated as induction of cancer cell apoptosis. However, more understanding on cancer cell type specific action of SPD-anticancer effects needs to be evaluated. HCT-116 cell line, a type of human colon carcinoma, was used to study SPD-anticancer effect. It was found that SPD concentration as low as 0.25 μM was able to inhibit 80% growth of cancer cells. IC_(50) value of SPD for HCT-116 was found to be 0.038 μM. Neurotoxicity test, carried out to determine the adverse effect of SPD towards nerve cells, gives CC_(50) value as 4.88 μM, thus concluded it to be a neurotoxic compound.
机译:由于癌症导致的死亡越来越多地强调了新的抗癌剂的需要。 先前发现Styrylpyrone衍生物(SPD)对许多类型的癌症具有潜在的抗癌作用。 一些SPD抗癌机制被阐明作为癌细胞凋亡的诱导。 然而,需要评估对癌细胞类型的对癌细胞类型的特异性作用进行更多的理解。 HCT-116细胞系,一种人结肠癌,用于研究SPD-抗癌效果。 发现低至0.25μm的SPD浓度能够抑制癌细胞的80%生长。 HCT-116的SPD的IC_(50)值被发现为0.038μm。 进行神经毒性测试,以确定SPD对神经细胞的不良影响,使CC_(50)值为4.88μm,因此将其结束为神经毒性化合物。

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