A novel chemopreventive mechanism for a traditional medicine: East Indian sandalwood oil induces autophagy and cell death in proliferating keratinocytes

被引:24
作者
Dickinson, Sally E. [1 ,2 ]
Olson, Erik R. [1 ,3 ]
Levenson, Corey [6 ]
Janda, Jaroslav [1 ]
Rusche, Jadrian J. [1 ]
Alberts, David S. [1 ,5 ]
Bowden, G. Timothy [1 ,4 ]
机构
[1] Univ Arizona, Arizona Canc Ctr, Tucson, AZ USA
[2] Univ Arizona, Dept Pharmacol, Tucson, AZ USA
[3] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[4] Univ Arizona, Dept Cellular & Mol Med, Tucson, AZ USA
[5] Univ Arizona, Dept Med, Tucson, AZ USA
[6] Santalis Pharmaceut Inc, San Antonio, TX USA
关键词
Sandalwood oil; Ultraviolet light; Cell death; Autophagy; SKIN TUMOR-DEVELOPMENT; ALPHA-SANTALOL; ACTIVATOR PROTEIN-1; CANCER; EXPRESSION; BINDING; AGENT;
D O I
10.1016/j.abb.2014.06.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
One of the primary components of the East Indian sandalwood oil (EISO) is alpha-santalol, a molecule that has been investigated for its potential use as a chemopreventive agent in skin cancer. Although there is some evidence that alpha-santalol could be an effective chemopreventive agent, to date, purified EISO has not been extensively investigated even though it is widely used in cultures around the world for its health benefits as well as for its fragrance and as a cosmetic. In the current study, we show for the first time that EISO-treatment of HaCaT keratinocytes results in a blockade of cell cycle progression as well as a concentration-dependent inhibition of UV-induced AP-1 activity, two major cellular effects known to drive skin carcinogenesis. Unlike many chemopreventive agents, these effects were not mediated through an inhibition of signaling upstream of AP-1, as EISO treatment did not inhibit UV-induced Akt or MAPK activity. Low concentrations of EISO were found to induce HaCaT cell death, although not through apoptosis as annexin V and PARP cleavage were not found to increase with EISO treatment. However, plasma membrane integrity was severely compromised in EISO-treated cells, which may have led to cleavage of LC3 and the induction of autophagy. These effects were more pronounced in cells stimulated to proliferate with bovine pituitary extract and EGF prior to receiving EISO. Together, these effects suggest that EISO may exert beneficial effects upon skin, reducing the likelihood of promotion of pre-cancerous cells to actinic keratosis (AK) and skin cancer. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 152
页数:10
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