Ganoderma lucidum Extract Reduces the Motility of Breast Cancer Cells Mediated by the RAC-Lamellipodin Axis

被引:18
作者
Acevedo-Diaz, Ariana [1 ]
Ortiz-Soto, Gabriela [2 ]
Suarez-Arroyo, Ivette J. [2 ]
Zayas-Santiago, Astrid [3 ]
Montemayor, Michelle M. Martinez [2 ]
机构
[1] Univ Puerto Rico Bayamon, Dept Biol, Bayamon, PR 00959 USA
[2] Univ Cent Caribe, Sch Med, Dept Biochem, Bayamon, PR 00960 USA
[3] Univ Cent Caribe, Sch Med, Dept Pathol & Lab Med, Bayamon, PR 00960 USA
基金
美国国家卫生研究院;
关键词
breast cancer; cancer cell migration; Ganoderma lucidum; lamellipodin; Rac; ACTIN CYTOSKELETON; MOLECULAR ASPECTS; RHO GTPASES; MIGRATION; GROWTH; INHIBITION; ENA/VASP; DYNAMICS; ESTROGEN; RECEPTOR;
D O I
10.3390/nu11051116
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Breast cancer (BC) is the second leading cause of cancer death among women worldwide. The main cause of BC morbidity and mortality is the invasiveness capacity of cancer cells that may lead to metastasis. Here, we aimed to investigate the therapeutic efficacy of Ganoderma lucidum extract (GLE)a medicinal mushroom with anticancer propertieson BC motility via the Rac/Lamellipodin pathway. GLE treatment effects were tested on MDA-MB-231 breast cancer cells. The effects were tested on cell viability, migration and invasion. Pulldowns, immunoblotting, and immunofluorescence were used to measure Rac activity and the expression of proteins involved in cell migration and in lamellipodia formation, respectively. As a result, GLE suppressed BC cell viability, migration, and invasion capacity. GLE impaired Rac activity, as well as downregulated Lamellipodin, ENA/VASP, p-FAK (Tyr925), Cdc42, and c-Myc expression. Lamellipodia formation was significantly reduced by GLE. In conclusion, we demonstrate that GLE reduces Rac activity and downregulates signaling molecules involved in lamellipodia formation. These novel findings serve as basis for further studies to elucidate the potential of GLE as a therapeutic agent regulating the Rac/Lamellipodin pathway in BC metastasis.
引用
收藏
页数:14
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