Haque Md Anwarul, Islam Md Anwar Ul
Department of Experimental Pathology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
Medicina (Kaunas). 2019 Oct 28;55(11):716. doi: 10.3390/medicina55110716.
: Mushrooms that have medicinal properties are part of many traditional diets. The aim of the present study was to use the human breast cancer cell line MCF-7 to investigate the anticancer activity of mushroom purified extract fraction-III (PEF-III) and to elucidate the possible mechanism of that activity. : The effects of PEF-III on cell proliferation and viability were evaluated by a colony formation assay and an MTT assay, respectively. Cell morphological changes, annexin-V phycoerythrin and propidium iodide (PI) staining, DNA fragmentation, and caspase 3/7 activity assays were performed to determine the induction of apoptosis by PEF-III. The genes responsible for regulation of apoptosis were analyzed by means of Western blot analysis. In vitro tumor sphere formation assay was performed using a 3D sphere culture system. : PEF-III significantly reduced the proliferation and viability of MCF-7 cells. Cell shrinkage and rounding, and annexin-V phycoerythrin and PI staining followed by flow cytometry indicated that the cell death was due to apoptosis. Additionally, a laddering DNA pattern and increased levels of caspase-3/7 enzyme also corroborated the notion of apoptosis-mediated cell death. This incidence was further confirmed by upregulation of proapoptotic genes ( and its target gene, ) and downregulation of the expression of an antiapoptotic gene (). PEF-III also reduced the size and number of the tumor spheres in 3D culture conditions. : The anticancer activity of PEF-III is due to induction of apoptosis by a shift in the balance of proapoptotic and antiapoptotic genes. Therefore, the findings of the present study may open a path to exploring potential drug candidates from the mushroom for combating breast cancer.
具有药用特性的蘑菇是许多传统饮食的一部分。本研究的目的是使用人乳腺癌细胞系MCF-7来研究蘑菇纯化提取物组分III(PEF-III)的抗癌活性,并阐明该活性可能的机制。
通过集落形成试验和MTT试验分别评估PEF-III对细胞增殖和活力的影响。进行细胞形态变化、膜联蛋白-V藻红蛋白和碘化丙啶(PI)染色、DNA片段化以及半胱天冬酶3/7活性测定,以确定PEF-III诱导的细胞凋亡。通过蛋白质免疫印迹分析来分析负责细胞凋亡调节的基因。使用三维球体培养系统进行体外肿瘤球体形成试验。
PEF-III显著降低了MCF-7细胞的增殖和活力。细胞收缩和变圆,以及膜联蛋白-V藻红蛋白和PI染色,随后进行流式细胞术分析表明细胞死亡是由于凋亡。此外,DNA梯形条带模式和半胱天冬酶-3/7酶水平的增加也证实了凋亡介导的细胞死亡这一观点。促凋亡基因(及其靶基因)的上调和抗凋亡基因()表达的下调进一步证实了这种情况。PEF-III在三维培养条件下也减小了肿瘤球体的大小并减少了其数量。
PEF-III的抗癌活性归因于促凋亡和抗凋亡基因平衡的改变所诱导的细胞凋亡。因此,本研究的结果可能为从蘑菇中探索对抗乳腺癌的潜在候选药物开辟一条道路。