Oncotarget

Reviews:

Cell penetrating peptides in preclinical and clinical cancer diagnosis and therapy

Prem Prakash Tripathi, Hamed Arami, Ivneet Banga, Jalaj Gupta and Sonu Gandhi _

PDF  |  HTML  |  How to cite  |  Order a Reprint

Oncotarget. 2018; 9:37252-37267. https://doi.org/10.18632/oncotarget.26442

Metrics: PDF 1334 views  |   HTML 2794 views  |   ?  


Abstract

Prem Prakash Tripathi1,2, Hamed Arami3,4, Ivneet Banga5, Jalaj Gupta6 and Sonu Gandhi7

1CSIR-Indian Institute of Chemical Biology (CSIR-IICB), Kolkata, India

2IICB-Translational Research Unit of Excellence, Kolkata, India

3Molecular Imaging Program at Stanford (MIPS), The James H. Clark Center, Stanford University, Stanford, CA, USA

4Department of Radiology, Stanford University, School of Medicine, Stanford, CA, USA

5Department of Bioengineering, University of Texas, Arlington, TX, USA

6Institute for Tumor Biology and Experimental Therapy, Georg-Speyer-Haus, Frankfurt, Germany

7DBT-National Institute of Animal Biotechnology (DBT-NIAB), Hyderabad, India

Correspondence to:

Sonu Gandhi, email: gandhi@niab.org.in

Prem Prakash Tripathi, email: prem.tripathi@iicb.res.in

Keywords: cell penetrating peptides; cancer targeting; therapy; diagnostic; imaging

Received: September 07, 2018     Accepted: November 29, 2018     Published: December 14, 2018

ABSTRACT

Delivery of imaging reagents and drugs to tumors is essential for cancer diagnosis and therapy. In addition to therapeutic and diagnostic functionalities, peptides have potential benefits such as biocompatibility, ease to synthesize, smaller size, by-passing off-target side effects, and achieving the beneficial effects with lower-administered dosages. A particular type of peptide known as cell penetrating peptides (CPP) have been predominantly studied during last twenty years as they are not only capable to translocate themselves across membranes but also allow carrier drugs to translocate across plasma membrane, by different mechanisms depending on the CPP. This is of great potential importance in drug delivery systems, as the ability to pass across membranes is crucial to many drug delivery systems. In spite of significant progress in design and application of CPP, more investigations are required to further improve their delivery to tumors, with reduced side-effect and enhanced therapeutic efficacy. In this review, we emphasis on current advancements in preclinical and clinical trials based on using CPP for more efficient delivery of anti-cancer drugs and imaging reagents to cancer tissues and individual cells associated with them. We discuss the evolution of the CPPs-based strategies for targeted delivery, their current status and strengths, along with summarizing the role of CPPs in targeted drug delivery. We also discuss some recently reported diagnostic applications of engineered protease-responsive substrates and activable imaging complexes. We highlight the recent clinical trial data by providing a road map for better design of the CPPs for future preclinical and clinical applications.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 26442