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菊苣来源的纤维素纳米晶体:通过 PI3K/AKT/mTOP 信号通路在乳腺癌细胞中作为芳香酶的非竞争性抑制剂。

Cellulose nanocrystals derived from chicory plant: an un-competitive inhibitor of aromatase in breast cancer cells via PI3K/AKT/mTOP signalling pathway.

机构信息

Department of Biochemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.

Department of Chemistry, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.

出版信息

J Biomol Struct Dyn. 2024 Jul;42(11):5575-5589. doi: 10.1080/07391102.2023.2226751. Epub 2023 Jun 20.

Abstract

A significant contributing factor in the development of breast cancer is the estrogens. The synthesis of estrogens is primarily facilitated by aromatase (CYP19), a cytochrome P450 enzyme. Notably, aromatase is expressed at a higher level in human breast cancer tissue compared with the normal breast tissue. Therefore, inhibiting aromatase activity is a potential strategy in hormone receptor-positive breast cancer treatment. In this study, Cellulose Nanocrystals (CNCs) were obtained from Chicory plant waste through a sulfuric acid hydrolysis method with the objective of investigating that whether the obtained CNCs could act as an inhibitor of aromatase enzyme, and prevent the conversion of androgens to estrogens. Structural analysis of CNCs was carried out using Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD), while morphological results were obtained using AFM, TEM, and FE-SEM. Furthermore, the nano-particles were found to be spherical in shape with a diameter range of 35-37 nm and displayed a reasonable negative surface charge. Stable transfection of MCF-7 cells with CYP19 has demonstrated the ability of CNCs to inhibit aromatase activities and prevent cell growth by interfering with the enzyme activities. Spectroscopic results revealed the binding constant of CYP19-CNCs and (CYP19-Androstenedione)-CNCs complexes to be 2.07 × 10 L/gr and 2.06 × 10 L/gr, respectively. Conductometry and CD data reported different interaction behaviors among CYP19 and CYP19-Androstenedione complexes at the presence of CNCs in the system. Moreover, the addition of CNCs to the solution in a successive manner resulted in the enhancement of the secondary structure of the CYP19-androstenedione complex. Additionally, CNCs showed a marked reduction in the viability of cancer cells compared to normal cells by enhancing the expression of Bax and p53 at protein and mRNA levels, and by decreasing mRNA levels of PI3K, AKT, and mTOP, as well as protein levels of PI3Kg-P110 and P-mTOP, in MCF-7 cells after incubation with CNCs at IC concentration. These findings confirm the decrease in proliferation of breast cancer cells associated with induction of apoptosis through down-regulation of the PI3K/AKT/mTOP signaling pathway. According to the provided data, the obtained CNCs are capable of inhibiting aromatase enzyme activity, which has significant implications for the treatment of cancer.Communicated by Ramaswamy H. Sarma.

摘要

乳腺癌发展的一个重要因素是雌激素。雌激素的合成主要由细胞色素 P450 酶芳香化酶(CYP19)促进。值得注意的是,芳香化酶在人乳腺癌组织中的表达水平明显高于正常乳腺组织。因此,抑制芳香化酶活性是治疗激素受体阳性乳腺癌的一种潜在策略。在这项研究中,通过硫酸水解法从菊苣植物废物中获得了纤维素纳米晶体(CNC),目的是研究所得的 CNC 是否可以作为芳香酶抑制剂,防止雄激素转化为雌激素。使用傅里叶变换红外光谱(FTIR)和 X 射线衍射(XRD)对 CNCs 进行结构分析,使用 AFM、TEM 和 FE-SEM 获得形态结果。此外,纳米颗粒呈球形,直径范围为 35-37nm,并显示出合理的负表面电荷。用 CYP19 稳定转染 MCF-7 细胞表明,CNC 能够通过干扰酶活性来抑制芳香酶活性并阻止细胞生长。光谱结果表明 CYP19-CNCs 和(CYP19-Androstenedione)-CNCs 复合物的结合常数分别为 2.07×10 L/gr 和 2.06×10 L/gr。电导率和 CD 数据报告了在系统中存在 CNCs 的情况下,CYP19 和 CYP19-Androstenedione 复合物之间不同的相互作用行为。此外,以连续的方式向溶液中添加 CNCs 会增强 CYP19-androstenedione 复合物的二级结构。此外,与正常细胞相比,CNC 可显著降低乳腺癌细胞的活力,通过在 MCF-7 细胞中增加 Bax 和 p53 的蛋白和 mRNA 水平的表达,并降低 PI3K、AKT 和 mTOP 的 mRNA 水平以及 PI3Kg-P110 和 P-mTOP 的蛋白水平,在 CNC 孵育后。这些发现证实了与通过下调 PI3K/AKT/mTOP 信号通路诱导细胞凋亡相关的乳腺癌细胞增殖减少。根据提供的数据,所得的 CNC 能够抑制芳香酶酶活性,这对癌症的治疗具有重要意义。由 Ramaswamy H. Sarma 传达。

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