Plant thymidine kinase 1: a novel efficient suicide gene for malignant glioma therapy

Z Khan, W Knecht, M Willer, E Rozpedowska… - Neuro …, 2010 - academic.oup.com
The prognosis for malignant gliomas remains poor, and new treatments are urgently
needed. Targeted suicide gene therapy exploits the enzymatic conversion of a prodrug …

Enhancement of CPT-11 antitumor activity by adenovirus-mediated expression of β–glucuronidase in tumors

PT Huang, KC Chen, ZM Prijovich, TL Cheng… - Cancer gene …, 2011 - nature.com
CPT-11 is a clinically important prodrug that requires conversion into the active metabolite
SN-38, a potent topoisomerase I poison, for antitumor activity. However, SN-38 is rapidly …

Novel therapeutic strategies in human malignancy: combining immunotherapy and oncolytic virotherapy

P Sampath, SH Thorne - Oncolytic virotherapy, 2015 - Taylor & Francis
Results from randomized clinical trials over the last several years have finally begun to
demonstrate the potential of oncolytic viral therapies to treat a variety of cancers. One reason …

Advances in imaging gene-directed enzyme prodrug therapy

S Bhaumik - Current pharmaceutical biotechnology, 2011 - ingentaconnect.com
Gene-directed enzyme prodrug therapy (GDEPT) is one of the promising alternatives to
conventional chemotherapy. Suicide gene therapy based anticancer strategy involves …

Cell death mechanisms induced by CLytA-DAAO chimeric enzyme in human tumor cell lines

M Fuentes-Baile, P García-Morales… - International Journal of …, 2020 - mdpi.com
The combination of the choline binding domain of the amidase N-acetylmuramoyl-L-alanine
(CLytA)-D-amino acid oxidase (DAAO)(CLytA-DAAO) and D-Alanine induces cell death in …

[引用][C] 六味地黄丸对小鼠移植性肝癌自杀基因治疗的增效作用

杜标炎, 王慧峰, 谭宇蕙, 吴映雅, 张立群, 李杰芬… - 广州中医药大学学报, 2007

Gene Targeting and Subsequent Site-Specific Transgenesis at the β-actin (ACTB) Locus in Common Marmoset Embryonic Stem Cells

S Shiozawa, K Kawai, Y Okada, I Tomioka… - Stem cells and …, 2011 - liebertpub.com
Nonhuman primate embryonic stem (ES) cells have vast promise for preclinical studies.
Genetic modification in nonhuman primate ES cells is an essential technique for maximizing …

Insulators to improve the safety of retroviral vectors for HIV gene therapy

DL Browning, GD Trobridge - Biomedicines, 2016 - mdpi.com
Retroviral vector gene therapy is a promising approach to treating HIV-1. However,
integrated vectors are mutagens with the potential to dysregulate nearby genes and cause …

Soluble precipitable porphyrins for use in targeted molecular brachytherapy

Z Yao, KE Borbas, JS Lindsey - New Journal of Chemistry, 2008 - pubs.rsc.org
In a new therapy that aims to concentrate and immobilize therapeutic radionuclides in
nanoscale assemblies within solid tumors, a soluble precipitable reagent (SPR) is …

Strategies to achieve systemic delivery of therapeutic cells and microbes to tumors

SH Thorne - Expert opinion on biological therapy, 2007 - Taylor & Francis
In order to more effectively treat cancer, targeted delivery of therapeutic agents will be
needed. The creation of delivery vehicles capable of locating and entering tumors before …