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Arch Biochem Biophys. 2014 Sep 15;558:143-52. doi: 10.1016/j.abb.2014.06.021. Epub 2014 Jul 5.

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

Author information

1
Arizona Cancer Center, University of Arizona, Tucson, AZ, United States; Department of Pharmacology, University of Arizona, Tucson, AZ, United States. Electronic address: sdickinson@uacc.arizona.edu.
2
Arizona Cancer Center, University of Arizona, Tucson, AZ, United States; Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, United States.
3
Santalis Pharmaceuticals, Inc., San Antonio, TX, United States.
4
Arizona Cancer Center, University of Arizona, Tucson, AZ, United States.
5
Arizona Cancer Center, University of Arizona, Tucson, AZ, United States; Department of Medicine, University of Arizona, Tucson, AZ, United States.
6
Arizona Cancer Center, University of Arizona, Tucson, AZ, United States; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.

Abstract

One of the primary components of the East Indian sandalwood oil (EISO) is α-santalol, a molecule that has been investigated for its potential use as a chemopreventive agent in skin cancer. Although there is some evidence that α-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.

KEYWORDS:

Autophagy; Cell death; Sandalwood oil; Ultraviolet light

PMID:
25004464
PMCID:
PMC4172370
DOI:
10.1016/j.abb.2014.06.021
[Indexed for MEDLINE]
Free PMC Article

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