Biomol Ther  
Shikonin Exerts Cytotoxic Effects in Human Colon Cancers by Inducing Apoptotic Cell Death via the Endoplasmic Reticulum and Mitochondria-Mediated Pathways
Xia Han, Kyoung Ah Kang, Mei Jing Piao, Ao Xuan Zhen, Yu Jae Hyun, Hyun Min Kim, Yea Seong Ryu and Jin Won Hyun*
Jeju National University School of Medicine, Jeju 63243, Republic of Korea
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The first two authors contributed equally to this work.
Received: March 13, 2018; Revised: April 29, 2018; Accepted: May 3, 2018; Published online: June 21, 2018.
© The Korean Society of Applied Pharmacology. All rights reserved.

The apoptotic effects of shikonin (5,8-dihydroxy-2-[(1R)-1-hydroxy-4-methylpent-3-enyl]naphthalene-1,4-dione) on the human colon cancer cell line SNU-407 were investigated in this study. Shikonin showed dose-dependent cytotoxic activity against SNU-407 cells, with an estimated IC50 value of 3 μM after 48 h of treatment. Shikonin induced apoptosis, as evidenced by apoptotic body formation, sub-G1 phase cells, and DNA fragmentation. Shikonin induced apoptotic cell death by activating mitogen-activated protein kinase family members, and the apoptotic process was mediated by the activation of endoplasmic reticulum (ER) stress, leading to activation of the PERK/elF2α/CHOP apoptotic pathway, and mitochondrial Ca2+ accumulation. Shikonin increased mitochondrial membrane depolarization and altered the levels of apoptosis-related proteins, with a decrease in B cell lymphoma (Bcl)-2 and an increase in Bcl-2-associated X protein, and subsequently, increased expression of cleaved forms of caspase-9 and -3. Taken together, we suggest that these mechanisms, including MAPK signaling and the ER- and mitochondria-mediated pathways, may underlie shikonin-induced apoptosis related to its anticancer effect.
Keywords: Shikonin, Human colon cancer, Apoptosis, Mitochondria, Endoplasmic reticulum

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