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新型反式钯(II)配合物对人细胞的体外细胞毒性评估。

Evaluation of cytotoxicity of new trans-palladium(II) complex in human cells in vitro.

作者信息

Kontek Renata, Matławska-Wasowska Ksenia, Kalinowska-Lis Urszula, Kontek Bogdan, Ochocki Justyn

机构信息

Laboratory of Cytogenetics, University of Lodz, 12/16 Banacha St., 90-237 Łódź, Poland.

出版信息

Acta Pol Pharm. 2011 Jan-Feb;68(1):127-36.

Abstract

Studies of cytotoxicity allow to elucidate the mechanisms by which chemical compounds influence cells and tissues. On the basis of the structural analogy between platinum(II) and palladium(II) complexes, a variety of studies on palladium(II) compounds as potential anticancer drugs have been carried out (1, 2). The cytotoxicity was evaluated by MTT assay. Abilities of trans-palladium(II) complex containing diethyl (pyridin-2-ylmethyl)phosphates as non-leaving ligands (trans-[PdCl2(2-pmOpe 2)]) to induce apoptosis and necrosis in normal lymphocytes, A549 cells and HT29 cell lines were performed by use of fluorochrome staining. The obtained results revealed, that the new trans-palladium(II) complex was more cytotoxic against A549 and HT29 tumor cells than on the normal lymphocytes in vitro. The novel complex induces apoptosis in all tested cells, but in lymphocytes to a lesser degree. The compound tested also induced significant amounts of necrotic cells, which exceeded the level of apoptotic cell fractions. The results demonstrate that the trans-Pd(II) complex showed substantial cytotoxic activity against A549 and HT29 tumor cells and indicate that the new trans-palladium(II) complex effectively inhibited cancer cells growth.

摘要

细胞毒性研究有助于阐明化合物影响细胞和组织的机制。基于铂(II)和钯(II)配合物之间的结构相似性,已对钯(II)化合物作为潜在抗癌药物进行了各种研究(1,2)。通过MTT法评估细胞毒性。使用荧光染色法研究了含有二乙基(吡啶-2-基甲基)磷酸酯作为非离去配体的反式钯(II)配合物(反式-[PdCl2(2-pmOpe 2)])诱导正常淋巴细胞、A549细胞和HT29细胞系凋亡和坏死的能力。所得结果表明,新的反式钯(II)配合物在体外对A549和HT29肿瘤细胞的细胞毒性比对正常淋巴细胞更强。该新型配合物在所有测试细胞中均诱导凋亡,但在淋巴细胞中的诱导程度较小。所测试的化合物还诱导了大量坏死细胞,其数量超过了凋亡细胞分数水平。结果表明,反式钯(II)配合物对A549和HT29肿瘤细胞显示出显著的细胞毒性活性,并表明新的反式钯(II)配合物有效地抑制了癌细胞的生长。

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