K
Kong-Nan Zhao
Researcher at University of Queensland
Publications - 76
Citations - 1738
Kong-Nan Zhao is an academic researcher from University of Queensland. The author has contributed to research in topics: Cancer & Gene. The author has an hindex of 22, co-authored 69 publications receiving 1485 citations. Previous affiliations of Kong-Nan Zhao include Princess Alexandra Hospital & QIMR Berghofer Medical Research Institute.
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Journal ArticleDOI
The role of the PI3K/Akt/mTOR signalling pathway in human cancers induced by infection with human papillomaviruses
TL;DR: Improved understanding of the mechanism by which the PI3K/Akt/mTOR signalling pathway contributes to the immortalization and carcinogenesis of HPV-transduced cells will assist in devising novel strategies for preventing and treating HPV-induced cancers.
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Codon modified human papillomavirus type 16 E7 DNA vaccine enhances cytotoxic T-lymphocyte induction and anti-tumour activity
Wen Jun Liu,Fengguang Gao,Kong-Nan Zhao,Weiming Zhao,Germain Jithendra Fernando,Ranjeny Thomas,Ian H. Frazer +6 more
TL;DR: The data indicate that immunogenicity of an E7 polynucleotide vaccine can be enhanced by codon modification, however, this may be insufficient for priming E7 responses in animals with split tolerance to E7 as a consequence of expression of E7 in somatic cells.
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Polynucleotide viral vaccines: codon optimisation and ubiquitin conjugation enhances prophylactic and therapeutic efficacy.
Wen Jun Liu,Kong-Nan Zhao,Feng Guang Gao,Graham R. Leggatt,Germain J. P. Fernando,Ian H. Frazer +5 more
TL;DR: It is shown that the lack of immunogenicity of polynucleotide vaccines based on the L1 gene can be overcome with codon modified L1, which induces strong immune responses, including conformational virus neutralising antibody and delayed type hypersensitivity.
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Effects of Intestinal Microbial⁻Elaborated Butyrate on Oncogenic Signaling Pathways.
TL;DR: The low bioavailability of butyrate for medicinal applications may be overcome by several approaches including nano-delivery, analogue development and combination use with other anti-cancer agents or phytochemicals.
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Codon usage bias and A+T content variation in human papillomavirus genomes.
TL;DR: Analyzing the codon usage bias of eight open reading frames (ORFs) across up to 79 human papillomavirus (HPV) genotypes from three distinct phylogenetic groups suggests that specific codonusage bias and A+T content variation may somehow increase the replicational fitness of HPVs in mammalian epithelial cells, and have practical implications for gene therapy of HPV infection.