New imidazolidindionedioximes and their Pt(II) complexes: synthesis and investigation of their antitumoral activities on breast cancer cells.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of Chemical Research Pub Date : 2024-01-22 eCollection Date: 2024-01-01 DOI:10.55730/1300-0527.3681
Emrah Karahan, Tuğba Gençoğlu Katmerlikaya, Emel Önal, Aydan Dağ, Ayşe Gül Gürek, Vefa Ahsen
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Abstract

Breast cancer is one of the most common types of cancer worldwide and has the most lethality ratio for females among all cancers. Although current cancer therapeutics have made considerable advancements, there is still room for improvement in terms of efficacy. Many anticancer drugs have a risk of causing serious adverse effects due to their nonspecific cytotoxic effects on both tumor and healthy cells. New therapeutics might have a greater ability to kill cancer cells, reduce the volume of tumors, and improve overall therapy response rates. Herein, we report the efficient synthesis and characterization of three amphi vic-dioximes and their six novel mono-, which are extremely rare in platinum chemistry, and bisplatinum(II) complexes for breast cancer treatment. Antitumoral activities of Pt(II) complexes have been investigated on CCD-1079Sk healthy fibroblast cell line, MCF-7 and MDA-MB-231 human breast cancer cell lines. Cytotoxicity, cell cycle, and apoptotic assays were performed. All new Pt(II) complexes exhibited selective antiproliferative effects on breast cancer cells by showing less cytotoxicity to healthy cells than known anticancer drugs cisplatin and bicalutamide. In vitro studies show that these new Pt complexes have high anticancer and antiproliferative effects and may be new alternatives to existing anticancer drugs.

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新型咪唑烷吲哚二氧肟及其铂(II)配合物:合成及其对乳腺癌细胞抗肿瘤活性的研究。
乳腺癌是全球最常见的癌症之一,也是女性致死率最高的癌症。尽管目前的癌症疗法已经取得了长足的进步,但在疗效方面仍有改进的余地。许多抗癌药物由于对肿瘤细胞和健康细胞具有非特异性细胞毒性作用,有可能导致严重的不良反应。新疗法可能具有更强的杀灭癌细胞、缩小肿瘤体积和提高总体治疗反应率的能力。在此,我们报告了用于乳腺癌治疗的三种双沧海二氧肟及其六种新型单铂和双铂(II)配合物的高效合成和表征。在 CCD-1079Sk 健康成纤维细胞系、MCF-7 和 MDA-MB-231 人类乳腺癌细胞系上研究了铂(II)配合物的抗肿瘤活性。实验中进行了细胞毒性、细胞周期和细胞凋亡检测。与已知的抗癌药物顺铂和比卡鲁胺相比,所有新的铂(II)复合物对健康细胞的细胞毒性较低,对乳腺癌细胞具有选择性抗增殖作用。体外研究表明,这些新型铂配合物具有很强的抗癌和抗增殖作用,可能成为现有抗癌药物的新替代品。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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