Virotherapy research involves the development, exploration, and application of oncolytic viruses that combine direct killing of cancer cells by viral infection, replication, and spread …
Y Zhao, TMD Le, J Hong, A Jiao, AR Yoon, CO Yun - ACS nano, 2024 - ACS Publications
Systemic delivery of oncolytic adenovirus (oAd) for cancer gene therapy must overcome several limitations such as rapid clearance from the blood, nonspecific accumulation in the …
TG Cunliffe, EA Bates, AL Parker - Cancers, 2020 - mdpi.com
Simple Summary If harnessed appropriately, oncolytic viruses offer significant potential as anti-cancer agents. Such virotherapies can be engineered to replicate inside cancerous …
A Gryciuk, M Rogalska, J Baran, L Kuryk… - Cancers, 2023 - mdpi.com
Simple Summary Current cancer therapies are insufficient to cure advanced malignancies and cause off-target toxicity. Scientists have focused on developing new, more efficacious …
F Napolitano, S Di Somma, G Castellano, J Amato… - Cells, 2022 - mdpi.com
G-quadruplexes (G4s) are nucleic secondary structures characterized by G-tetrads. G4 motif stabilization induces DNA damage and cancer cell death; therefore, G4-targeting small …
J Doerner, E Sallard, W Zhang, M Solanki, J Liu… - Molecular Cancer …, 2022 - AACR
Oncolytic adenoviruses (OAd) represent an attractive treatment option for cancer. Clinical efficacy of commonly utilized human adenovirus type 5 (Ad5)-based oncolytic viruses is …
Pituitary tumor-transforming gene 1 (PTTG1) is overexpressed in various types of tumors and functions as an oncogene; it could also be a potential target in tumor therapy …
ID Osipov, VA Vasikhovskaia, DS Zabelina… - Viruses, 2023 - mdpi.com
Human Adenovirus type 6 (HAdV-C6) is a promising candidate for the development of oncolytic vectors as it has low seroprevalence and the intrinsic ability to evade tissue …
T Dong, JR Shah, AT Phung, C Larson, AB Sanchez… - Cancers, 2023 - mdpi.com
Simple Summary Oncolytic adenoviruses are genetically engineered to selectively replicate within cancer cells by exploiting their unique characteristics while sparing normal cells …