Deletion of F4L (ribonucleotide reductase) in vaccinia virus produces a selective oncolytic virus and promotes anti‐tumor immunity with superior safety in bladder cancer models-Reference-Cited by-同舟云学术

Deletion of F4L (ribonucleotide reductase) in vaccinia virus produces a selective oncolytic virus and promotes anti‐tumor immunity with superior safety in bladder cancer models

Published:2017-03-13 Issue:5 Volume:9 Page:638-654
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Potts Kyle G¹²³,Irwin Chad R²³⁴,Favis Nicole A²³⁴,Pink Desmond B¹³,Vincent Krista M¹³⁵,Lewis John D¹³^ORCID,Moore Ronald B¹³⁶,Hitt Mary M¹²³,Evans David H²³⁴^ORCID

Affiliation:

1. Department of Oncology Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada

2. Li Ka Shing Institute of Virology Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada

3. Cancer Research Institute of Northern Alberta (CRINA) Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada

4. Department of Medical Microbiology & Immunology Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada

5. Department of Anatomy & Cell Biology Faculty of Medicine and Dentistry University of Western Ontario London ON Canada

6. Department of Surgery Faculty of Medicine and Dentistry University of Alberta Edmonton AB Canada

Funder

Alberta Innovates - Health Solutions

Alberta Cancer Foundation

University of Alberta

Li Ka Shing Foundation

Canadian Institutes of Health Research

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201607296

Reference53 articles.

1. Best practice in the treatment of nonmuscle invasive bladder cancer

2. Talimogene Laherparepvec Improves Durable Response Rate in Patients With Advanced Melanoma

3. Successful Diagnosis Of Orthotopic Rat Superficial Bladder Tumor Model By Ultrathin Cystoscopy

4. Ribonucleotide reductase and cancer: biological mechanisms and targeted therapies

5. Stimulation of Autologous Antitumor T-Cell Responses Against Medullary Thyroid Carcinoma Using Tumor Lysate-Pulsed Dendritic Cells

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