Cell penetrating peptides, novel vectors for gene therapy

RE Taylor, M Zahid - Pharmaceutics, 2020 - mdpi.com
Cell penetrating peptides (CPPs), also known as protein transduction domains (PTDs), first
identified~ 25 years ago, are small, 6–30 amino acid long, synthetic, or naturally occurring …

High-capacity adenoviral vectors: expanding the scope of gene therapy

A Ricobaraza, M Gonzalez-Aparicio… - International Journal of …, 2020 - mdpi.com
The adaptation of adenoviruses as gene delivery tools has resulted in the development of
high-capacity adenoviral vectors (HC-AdVs), also known, helper-dependent or “gutless” …

The human glioblastoma cell culture resource: validated cell models representing all molecular subtypes

Y Xie, T Bergström, Y Jiang, P Johansson… - …, 2015 - thelancet.com
Glioblastoma (GBM) is the most frequent and malignant form of primary brain tumor. GBM is
essentially incurable and its resistance to therapy is attributed to a subpopulation of cells …

Current approaches in CRISPR-Cas9 mediated gene editing for biomedical and therapeutic applications

G Bhattacharjee, N Gohil, K Khambhati, I Mani… - Journal of Controlled …, 2022 - Elsevier
A single gene mutation can cause a number of human diseases that affect the quality of life.
Until the development of clustered regularly interspaced short palindromic repeats …

Safe engineering of CAR T cells for adoptive cell therapy of cancer using long‐term episomal gene transfer

C Jin, G Fotaki, M Ramachandran… - EMBO molecular …, 2016 - embopress.org
Chimeric antigen receptor (CAR) T‐cell therapy is a new successful treatment for refractory
B‐cell leukemia. Successful therapeutic outcome depends on long‐term expression of CAR …

Targeted adenovirus-mediated transduction of human T cells in vitro and in vivo

PC Freitag, M Kaulfuss, L Flühler, J Mietz… - … Therapy Methods & …, 2023 - cell.com
Clinical success in T cell therapy has stimulated widespread efforts to increase safety and
potency and to extend this technology to solid tumors. Yet progress in cell therapy remains …

Chondroitin Sulfate‐Coated DNA‐Nanoplexes Enhance Transfection Efficiency by Controlling Plasmid Release from Endosomes: A New Insight into Modulating …

H Yan, OP Oommen, D Yu, J Hilborn… - Advanced Functional …, 2015 - Wiley Online Library
Degradation of plasmid DNA (pDNA) in the endosome compartment and its release to the
cytosol are the major hurdles for efficient gene transfection. This is generally addressed by …

Expanding the spectrum of pancreatic cancers responsive to vesicular stomatitis virus-based oncolytic virotherapy: challenges and solutions

MC Holbrook, DW Goad, VZ Grdzelishvili - Cancers, 2021 - mdpi.com
Simple Summary Pancreatic ductal adenocarcinoma (PDAC) is a devastating malignancy
with a poor prognosis and a dismal survival rate. Oncolytic virus (OV) is an anticancer …

Nonreplicating adenoviral vectors: improving tropism and delivery of cancer gene therapy

NG Tessarollo, ACM Domingues, F Antunes, JCS Luz… - Cancers, 2021 - mdpi.com
Simple Summary The treatment of cancer has progressed greatly with the advent of
immunotherapy and gene therapy, including the use of nonreplicating adenoviral vectors to …

An infection-enhanced oncolytic adenovirus secreting H. pylori neutrophil-activating protein with therapeutic effects on neuroendocrine tumors

M Ramachandran, D Yu, A Wanders, M Essand… - Molecular Therapy, 2013 - cell.com
Helicobacter pylori neutrophil-activating protein (HP-NAP) is a major virulence factor
involved in H. pylori infection. HP-NAP can mediate antitumor effects by recruiting …