Procyanidins from Vitis vinifera seeds induce apoptotic and autophagic cell death via generation of reactive oxygen species in squamous cell carcinoma cells

被引:21
作者
Hah, Young-Sool [1 ]
Kim, Jin Gu [2 ]
Cho, Hee Young [1 ]
Park, Jin Sung [3 ]
Heo, Eun Phil [4 ]
Yoon, Tae-Jin [2 ]
机构
[1] Gyeongsang Natl Univ, Biomed Res Inst, Gyeongsang Natl Univ Hosp, Sch Med, Jinju 52727, Gyeongsangnam D, South Korea
[2] Gyeongsang Natl Univ, Dept Dermatol, Gyeongsang Natl Univ Hosp, Sch Med,Inst Hlth Sci, 79 Gangnam Ro, Jinju 52727, Gyeongsangnam D, South Korea
[3] Gyeongsang Natl Univ Hosp, Dept Orthoped Surg, Jinju 52727, Gyeongsangnam D, South Korea
[4] Sungkyunkwan Univ, Dept Dermatol, Sch Med, Samsung Changwon Hosp, Chang Won 51353, Gyeongsangnam D, South Korea
基金
新加坡国家研究基金会;
关键词
procyanidins; squamous cell carcinoma; anticancer activity; apoptosis; autophagy; GRAPE SEEDS; IN-VITRO; PROANTHOCYANIDINS; EXTRACT; ACTIVATION; DISEASE; PROTEIN; GROWTH;
D O I
10.3892/ol.2017.6422
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Procyanidins can inhibit cell proliferation and tumorigenesis and induce apoptosis in human skin, breast and prostate carcinoma cell lines. Squamous cell carcinoma (SCC) of the skin is a common form of keratinocytic or non-melanoma skin cancer and is a deadly disease with a poor prognosis due to the ineffectiveness of therapy. The present study aimed to determine whether grape seed proanthocyanidin (GSP) may regulate different modes of cell death in the human SCC12 cell line. The present study found that the treatment of SCC12 cells with GSP inhibited proliferation in a dose-dependent manner and reduced the motility and invasiveness of SCC12 cells through suppression of matrix metalloproteinase-2/9 expression. GSP treatment also resulted in induction of apoptosis and autophagy via generation of reactive oxygen species. The inhibition of autophagy by 3-methyladenine decreased GSP-induced cell death, which suggested that GSP-induced autophagy can promote cell death. The results of the present study suggested that autophagy functions as a death mechanism in SCC and provided a rationale for the use of GSP in combination with autophagy activators for treating cancers such as SCC.
引用
收藏
页码:1925 / 1932
页数:8
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