Special Issue "Emerging Anti-cancer and Cellular Targets and Their Mechanism(s) of Action as New Tools for Therapeutics Approaches"

A special issue of Pharmaceutics (ISSN 1999-4923). This special issue belongs to the section "Drug Targeting and Design".

Deadline for manuscript submissions: 30 August 2023 | Viewed by 709

Special Issue Editors

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale Ferdinando Stagno D׳Alcontres, 31-98166 Messina, Italy
Interests: neuroinflammation; central nervous system; degeneration; molecular pathways; protein trafficking
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale Ferdinando Stagno D׳Alcontres, 31-98166 Messina, Italy
Interests: molecular biology; biotechnology; neuroinflammation; central nervous system; molecular pathways

Special Issue Information

Dear Colleagues,

Cancer cells at the center of tumors respond to varied local hypoxic conditions, activating signaling pathways and promoting synthesis and release of chemokines and growth factors (GFs) that transform the local environment. Immune, endothelial, and neuronal, among other cell types, express receptors that respond to these oncogenic signals. In this process, cancer cells with invasive and anchorage-free survival properties could disseminate and establish metastatic tumors. Thus, targeting and understanding the communication between tumor cells and the adjacent vasculature is the basis of novel anti-tumor therapies. More recent studies have identified abrupt cellular signaling pathways as underlying mechanisms for the development of cancer drug resistance. Some key processes involved in drug resistance include tumor heterogeneity, reactivation of drug targets, hyperactivation of alternative pathways, cross-talk with the microenvironment, altered DNA response and its repair, modification in epigenetic pathways, impairment in apoptosis/autophagy and the existence of cancer stem cells. Thus, increased understanding of the mechanisms underlying cancer drug resistance suggests that an integrated approach to cancer therapy is needed for targeting multiple signaling pathways. Recent use of molecularly targeted agents to target multiple signaling pathways remains an important approach in cancer treatment; however, use of these targeted therapies is not without limitations. Further research is needed to identify approaches to repurpose drugs to optimize therapy for particular cancer types.

This Special Issue will focus on cellular targets and their mechanisms for many types of cancers, including cancer therapeutic approaches and targeted drug delivery. We are pleased to invite authors to submit contributions, such as original articles that provide novel findings, or reviews that comprehensively highlight the latest discoveries in the field.

In this Special Issue, original research articles and reviews are welcome. Research areas may include (but are not limited to) the following:

  • Immune system;
  • SNC;
  • Antibodies therapies;
  • Peripheral tumors;
  • Circulating tumors;
  • Protein degradation;
  • Cell death mechanism;
  • Inflammatory pathways.

I/We look forward to receiving your contributions. 

Dr. Alessia Filippone
Dr. Marika Lanza
Guest Editors

Manuscript Submission Information

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Pharmaceutics is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • neurogenesis
  • immune evasion
  • endogenous tumor targets
  • CNS
  • neuroinflammation
  • protein degradation
  • receptors activation
  • cancerous cells invasion
  • molecular pathways

Published Papers (1 paper)

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Research

Article
In Silico and In Vivo Studies of a Tumor-Penetrating and Interfering Peptide with Antitumoral Effect on Xenograft Models of Breast Cancer
Pharmaceutics 2023, 15(4), 1180; https://doi.org/10.3390/pharmaceutics15041180 - 07 Apr 2023
Viewed by 577
Abstract
The combination of a tumor-penetrating peptide (TPP) with a peptide able to interfere with a given protein–protein interaction (IP) is a promising strategy with potential clinical application. Little is known about the impact of fusing a TPP with an IP, both in terms [...] Read more.
The combination of a tumor-penetrating peptide (TPP) with a peptide able to interfere with a given protein–protein interaction (IP) is a promising strategy with potential clinical application. Little is known about the impact of fusing a TPP with an IP, both in terms of internalization and functional effect. Here, we analyze these aspects in the context of breast cancer, targeting PP2A/SET interaction, using both in silico and in vivo approaches. Our results support the fact that state-of-the-art deep learning approaches developed for protein–peptide interaction modeling can reliably identify good candidate poses for the IP-TPP in interaction with the Neuropilin-1 receptor. The association of the IP with the TPP does not seem to affect the ability of the TPP to bind to Neuropilin-1. Molecular simulation results suggest that peptide IP-GG-LinTT1 in a cleaved form interacts with Neuropilin-1 in a more stable manner and has a more helical secondary structure than the cleaved IP-GG-iRGD. Surprisingly, in silico investigations also suggest that the non-cleaved TPPs can bind the Neuropilin-1 in a stable manner. The in vivo results using xenografts models show that both bifunctional peptides resulting from the combination of the IP and either LinTT1 or iRGD are effective against tumoral growth. The peptide iRGD-IP shows the highest stability to serum proteases degradation while having the same antitumoral effect as Lin TT1-IP, which is more sensitive to proteases degradation. Our results support the development of the TPP-IP strategy as therapeutic peptides against cancer. Full article
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