新合成的钯(II)配合物诱导的细胞毒性导致MCF-7和MDA-MB-435癌细胞死亡

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Bruna Alexandre Oliveira da Silva, Isabela Spido Dias, Luís Eduardo Sarto, Elba Pereira de Gois, Claudia Torres, Eduardo Tonon de Almeida, Cibele Marli Cação Paiva Gouvêa
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引用次数: 1

摘要

目的:乳腺癌是最常见的女性恶性肿瘤,黑色素瘤是最致命的皮肤癌类型。传统的癌症治疗方法由于耐药和副作用,远远不能令人满意,因此正在强调寻找新的药物。钯(II)配合物已被报道为潜在的抗癌药物。在这项工作中,评估了一系列新的方形平面Pd(II)复合物对MCF-7和MDA-MB-435癌细胞的抗癌活性和细胞死亡诱导。方法:培养MCF-7(乳腺癌)和MDA-MB-435(黑色素瘤)细胞,用配体和Pd(II)复合物处理。研究了处理后细胞的生长、迁移和粘附抑制、形态改变、细胞死亡诱导和DNA相互作用。结果:Pd(II)复合物对两种细胞系都表现出短期和长期的抗增殖作用,在SRB实验中降低了80%的细胞生长,并通过克隆生成实验估计消除了长期的增殖。结论:总的来说,复合物具有细胞毒活性并诱导细胞死亡。这些观察结果强调了Pd(II)复合物在改善乳腺癌和黑色素瘤患者预后方面的抗癌作用和潜在的治疗价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cytotoxicity Induced by Newly Synthesized Palladium (II) Complexes Lead to the Death of MCF-7 and MDA-MB-435 Cancer Cell Lines.

Cytotoxicity Induced by Newly Synthesized Palladium (II) Complexes Lead to the Death of MCF-7 and MDA-MB-435 Cancer Cell Lines.

Cytotoxicity Induced by Newly Synthesized Palladium (II) Complexes Lead to the Death of MCF-7 and MDA-MB-435 Cancer Cell Lines.

Cytotoxicity Induced by Newly Synthesized Palladium (II) Complexes Lead to the Death of MCF-7 and MDA-MB-435 Cancer Cell Lines.

Purpose: Breast cancer is the most common female malignancy and melanoma is the most lethal type of skin cancer. Traditional therapy for cancer treatment is far from satisfactory due to drug resistance and side effects, thus a search for new medicines is being emphasized. Palladium(II) complexes have been reported as anticancer potential agents. In this work, the anticancer activities and cell death induction of a new series of square-planar Pd(II) complexes were evaluated against MCF-7 and MDA-MB-435 cancer cells. Methods: MCF-7 (breast carcinoma) and MDA-MB-435 (melanoma) cells were cultivated, and treated with ligand and Pd(II) complexes. Cell growth, migration and adhesion inhibition, morphological alterations, cell death induction and, DNA interaction upon treatment were studied. Results: Pd(II) complexes exhibited both short and long-term antiproliferative effects on both cell lines, reducing by 80% cell growth in the SRB assay and abolishing longterm proliferation, estimated by the clonogenic assay. Complexes reduced significantly (P<0.05) cell migration and adhesion when compared to the control group. Complexes induced morphological alterations in cell lines and significant (P<0.05) cellular shrinkage. Cell death was induced and the complexes were able to interact with DNA, inducing cleavage of double-stranded DNA, which may account for the complexes cytotoxic effects, observed against both MCF-7 and MDA-MB-435 cells. Conclusion: Overall, the complexes exhibited cytotoxic activities and induced cell death. These observations emphasize an anticancer role with a potential therapeutic value for Pd(II) complexes to improve the outcome of patients with breast cancer and melanoma.

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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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