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微藻提取物抑制乳腺癌细胞的增殖、侵袭并诱导其凋亡。

Microalgae Extract Inhibits Proliferation, Invasion, and Induces Apoptosis in Breast Cancer Cells.

作者信息

Alateyah Nouralhuda, Ahmad Salma M S, Gupta Ishita, Fouzat Arij, Thaher Mahmoud Ibrahim, Das Probir, Al Moustafa Ala-Eddin, Ouhtit Allal

机构信息

Biological Sciences Program, Department of Biological and Environmental Sciences, College of Arts and Sciences, Qatar University, Doha, Qatar.

College of Medicine, Qatar University, Doha, Qatar.

出版信息

Front Nutr. 2022 May 11;9:882956. doi: 10.3389/fnut.2022.882956. eCollection 2022.

Abstract

Breast cancer (BC) is the most common malignant cancer in females worldwide. Drug resistance, toxicity, and the failure of current therapies to completely cure BC has challenged conventional medicine. Consequently, complementary alternative medicine has become popular due to its safety and efficacy. () is a green microalga living in fresh water, and its crude extract is rich of bioactives, including carotenoids, known to inhibit cancer cell growth. In the present study, we investigated the effects of a methanol crude extract called "T1" of on cell growth and migration/invasion of the BC cell line MDA-MB-231 in comparison to the fibroblast control cells. TI significantly suppressed BC cell growth, inhibited migration and invasion and induced apoptosis. Interestingly, apoptosis was mediated by a significant loss of mutant p53 protein, and increased Bax/Bcl2 ratio. Our findings support our hypothesis that T1 exerts its anti-cancer effects by inhibiting BC invasion and inducing apoptosis mediated, at least, the p53/Bax/Bcl2 pathway. Ongoing experiments aim to identify the molecular mechanisms underpinning T1-inhibited BC cell invasion using pre-designed metastasis gene-based array method.

摘要

乳腺癌(BC)是全球女性中最常见的恶性肿瘤。耐药性、毒性以及当前治疗方法无法完全治愈BC对传统医学提出了挑战。因此,补充替代医学因其安全性和有效性而受到欢迎。()是一种生活在淡水中的绿色微藻,其粗提物富含生物活性物质,包括已知可抑制癌细胞生长的类胡萝卜素。在本研究中,我们研究了一种名为“T1”的甲醇粗提物与成纤维细胞对照细胞相比,对BC细胞系MDA-MB-231的细胞生长和迁移/侵袭的影响。T1显著抑制BC细胞生长,抑制迁移和侵袭并诱导凋亡。有趣的是,凋亡是由突变型p53蛋白的显著缺失和Bax/Bcl2比值增加介导的。我们的研究结果支持了我们的假设,即T1通过抑制BC侵袭并诱导至少由p53/Bax/Bcl2途径介导的凋亡来发挥其抗癌作用。正在进行的实验旨在使用预先设计的基于转移基因的阵列方法确定T1抑制BC细胞侵袭的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/317a/9130701/3f37433a11c8/fnut-09-882956-g001.jpg

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