TY - JOUR
T1 - DNAzyme targeting c-jun suppresses skin cancer growth
AU - Cai, Hong
AU - Santiago, Fernando S.
AU - Prado-Lourenco, Leonel
AU - Wang, Bo
AU - Patrikakis, Margaret
AU - Davenport, Miles P.
AU - Maghzal, Ghassan J.
AU - Stocker, Roland
AU - Parish, Christopher R.
AU - Chong, Beng H.
AU - Lieschke, Graham J.
AU - Wong, Tak Wah
AU - Chesterman, Colin N.
AU - Francis, Douglas J.
AU - Moloney, Fergal J.
AU - Barnetson, Ross St C.
AU - Halliday, Gary M.
AU - Khachigian, Levon M.
PY - 2012/6/20
Y1 - 2012/6/20
N2 - Worldwide, one in three cancers is skin-related, with increasing incidence in many populations. Here, we demonstrate the capacity of a DNAzyme-targeting c-jun mRNA, Dz13, to inhibit growth of two common skin cancer types - basal cell and squamous cell carcinomas - in a therapeutic setting with established tumors. Dz13 inhibited tumor growth in both immunodeficient and immunocompetent syngeneic mice and reduced lung nodule formation in a model of metastasis. In addition, Dz13 suppressed neovascularization in tumor-bearing mice and zebrafish and increased apoptosis of tumor cells. Dz13 inhibition of tumor growth, which required an intact catalytic domain, was due in part to the induction of tumor immunity. In a series of good laboratory practice-compliant toxicology studies in cynomolgus monkeys, minipigs, and rodents, the DNAzyme was found to be safe and well tolerated. It also did not interfere in more than 70 physiologically relevant in vitro bioassays, suggesting a reduced propensity for off-target effects. If these findings hold true in clinical trials, Dz13 may provide a safe, effective therapy for human skin cancer.
AB - Worldwide, one in three cancers is skin-related, with increasing incidence in many populations. Here, we demonstrate the capacity of a DNAzyme-targeting c-jun mRNA, Dz13, to inhibit growth of two common skin cancer types - basal cell and squamous cell carcinomas - in a therapeutic setting with established tumors. Dz13 inhibited tumor growth in both immunodeficient and immunocompetent syngeneic mice and reduced lung nodule formation in a model of metastasis. In addition, Dz13 suppressed neovascularization in tumor-bearing mice and zebrafish and increased apoptosis of tumor cells. Dz13 inhibition of tumor growth, which required an intact catalytic domain, was due in part to the induction of tumor immunity. In a series of good laboratory practice-compliant toxicology studies in cynomolgus monkeys, minipigs, and rodents, the DNAzyme was found to be safe and well tolerated. It also did not interfere in more than 70 physiologically relevant in vitro bioassays, suggesting a reduced propensity for off-target effects. If these findings hold true in clinical trials, Dz13 may provide a safe, effective therapy for human skin cancer.
UR - http://www.scopus.com/inward/record.url?scp=84862841985&partnerID=8YFLogxK
U2 - 10.1126/scitranslmed.3003960
DO - 10.1126/scitranslmed.3003960
M3 - Article
SN - 1946-6234
VL - 4
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 139
M1 - 139ra82
ER -