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取代的“氨基-烷基-若丹明”衍生物对 MCF-7 人乳腺癌细胞系的抗癌潜力。

Anti-cancer potential of substituted "amino-alkyl-rhodamine" derivatives against MCF-7 human breast cancer cell line.

机构信息

Department of Pharmaceutical Sciences, Jharkhand Rai University, Ratu Road, Ranchi, 835222, Jharkhand, India.

Department of Pharmacology, Eminent College of Pharmaceutical Technology, Barasat, 700126, West Bengal, India.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2023 May;396(5):1001-1007. doi: 10.1007/s00210-022-02376-3. Epub 2023 Jan 3.

DOI:10.1007/s00210-022-02376-3
PMID:36595094
Abstract

Breast cancer is the most prevalent diagnosed cancer among women and the main cause of morbidity and mortality. As for breast cancer, MCF-7 cells are an important candidate since they are widely utilized in research for estrogen receptor (ER)-positive breast cancer cell assays, and various sub-clones have been identified to reflect different classes of ER-positive tumors with varied levels of nuclear receptor expression. Rhodamines and its derivatives have shown a great interest over the past two decades due to their excellent structural and spectroscopic properties. Rhodamine derivatives have been widely investigated for their mitochondrial targeting and chemotherapeutic properties. Rhodamine derivatives, in particular, have been widely investigated for their therapeutic properties. In this regard, several studies have shown that rhodamine dye derivatives have promising in vitro and in vivo therapeutic efficacy. The present study deals with potential anticancer activity of few synthesized rhodamine derivatives against MCF-7 cell lines.

摘要

乳腺癌是女性中最常见的诊断癌症,也是发病率和死亡率的主要原因。就乳腺癌而言,MCF-7 细胞是一个重要的候选细胞,因为它们广泛应用于研究雌激素受体 (ER) 阳性乳腺癌细胞的测定,并且已经鉴定出各种亚克隆来反映不同类别的 ER 阳性肿瘤,其核受体表达水平不同。近二十年来,由于罗丹明及其衍生物具有优异的结构和光谱性质,因此引起了人们的极大兴趣。罗丹明衍生物因其靶向线粒体和化疗特性而被广泛研究。罗丹明衍生物,特别是其治疗特性,已经得到了广泛的研究。在这方面,几项研究表明,罗丹明染料衍生物具有有前途的体外和体内治疗效果。本研究探讨了几种合成的罗丹明衍生物对 MCF-7 细胞系的潜在抗癌活性。

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本文引用的文献

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Selective pressure of endocrine therapy activates the integrated stress response through NFκB signaling in a subpopulation of ER positive breast cancer cells.内分泌治疗的选择压力通过 NFκB 信号通路在 ER 阳性乳腺癌细胞的亚群中激活整合应激反应。
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Preferences of rhodamine coupled (aminoalkyl)-piperazine probes towards Hg(II) ion and their FRET mediated signaling.吖啶酮偶联(氨烷基)-哌嗪探针对 Hg(II)离子的偏好及其荧光共振能量转移介导的信号传递。
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