粗神经孢子虫是乳腺癌抗癌药物的潜在来源。

IF 2.9
Breast cancer (Tokyo, Japan) Pub Date : 2022-11-01 Epub Date: 2022-07-05 DOI:10.1007/s12282-022-01383-9
Rui Han, Hongxing Yang, Changquan Ling, Lingeng Lu
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引用次数: 2

摘要

真菌是一种极好的药物来源,包括抗肿瘤药物。粗神经孢子虫产生的代谢物具有多种结构类别,但其作为抗肿瘤药物来源的潜力尚未得到探索。本研究旨在探讨粗神经孢子菌混合物对乳腺癌的潜在作用。体外T-47D和MDA-MB-231实验表明,1.7和0.85µg/ml浓度的草苔草混合物均能显著抑制肿瘤细胞的增殖、迁移和侵袭以及3D球体的形成。而MCF-10A在0.85和1.7µg/ml浓度下的抑制率为10-20%。浓度为0.85µg/ml的混合物可显著下调T-47D或MDA-MD-231乳腺癌细胞株中E2F1、E2F3转录因子、肿瘤干细胞相关基因LIN28、HIWI、CD133和onco-lncRNA HOTAIR的表达,提高CASP3活性。体内乳腺癌C3H小鼠模型实验结果显示,草苔草混合物明显抑制肿瘤生长。这些发现提示,草属植物含有抗乳腺癌侵袭性的抗肿瘤成分,其可能通过下调肿瘤干细胞相关和/或转录因子基因和癌基因,促进细胞凋亡,从而抑制乳腺癌干细胞的自我更新和分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurospora crassa is a potential source of anti-cancer agents against breast cancer.

Fungi are an excellent source of pharmaceuticals including anti-tumor agents. Neurospora crassa generates metabolites with diverse structural classes, however, its potential as an anti-tumor agent source has not been explored. The purpose of this study aimed to investigate the potential of Neurospora crassa mixture against breast cancer. The in vitro T-47D and MDA-MB-231 experiments showed that N. crassa mixture at the concentrations of both 1.7 and 0.85 µg/ml significantly inhibited tumor cell proliferation, migration and invasion, and 3D spheroid formation. However, the inhibition rates of MCF-10A ranged 10-20% at concentrations of 0.85 and 1.7 µg/ml. The mixture at the concentration of 0.85 µg/ml could significantly downregulate the expressions of transcription factors of E2F1 and E2F3, cancer stem cell-related genes of LIN28, HIWI, and CD133, and onco-lncRNA HOTAIR, and increase CASP3 activity in either T-47D or MDA-MD-231 breast cancer cell lines. In vivo breast cancer C3H mouse model results showed that N. crassa mixture significantly inhibited tumor growth. These findings suggest that N. crassa contains an antitumor component(s) against breast cancer invasiveness, which may inhibit the self-renewal and differentiation of breast cancer stem cells possibly by downregulating cancer stem cell-associated and/or transcription factor genes and oncogenes, and promoting apoptosis.

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