Literature DB >> 21864224

Blocking the interaction of vascular endothelial growth factor receptors with their ligands and their effector signaling as a novel therapeutic target for cancer: time for a new look?

David Bruce1, Peng H Tan.   

Abstract

INTRODUCTION: The interaction between the VEGFRs and their ligands plays an important role in tumor angiogenesis. Despite a series of problems encountered during early work on blocking growth factors, current evidence injects further vigor into researching the modulation of VEGFR activity. Emerging preclinical and clinical studies suggest that attenuating receptor activity can synergistically promote antitumor action if utilized concurrently with conventional therapies. AREAS COVERED: This review presents an up-to-date assessment of the potential role of modulating receptor activities in various cancers. The sentinel work on the proof of principles in various animal models, and the current translational research on these small molecule inhibitors and receptor blocking antibodies, from Phase I to Phase III trials, has been systematically examined with an emphasis on agents in earlier stages of development. EXPERT OPINION: Many clinical trials are ongoing, but early phase trials show promising results. Recently, there has been a huge explosion of research activity either in the development of new drugs or in the understanding its biology. Many current trials lend support to the rationale behind these therapies, which can function as adjuvants to conventional treatments. It has been argued that normalization of tumor-induced vasculature can promote better drug delivery and prevent resistance to radiotherapy. However, strategies involving the inhibition of the interaction of VEGFRs with ligands and their downstream pathways are not, in general, at a stage where it will be directly useful in clinical cancer treatment. A deeper understanding of these biologic therapies will help to improve the efficacy of conventional treatments and furthermore reduce dose-dependent cytotoxic activity.

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Year:  2011        PMID: 21864224     DOI: 10.1517/13543784.2011.611801

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  3 in total

1.  The functionalized human serine protease granzyme B/VEGF₁₂₁ targets tumor vasculature and ablates tumor growth.

Authors:  Khalid A Mohamedali; Yu Cao; Lawrence H Cheung; Walter N Hittelman; Michael G Rosenblum
Journal:  Mol Cancer Ther       Date:  2013-07-15       Impact factor: 6.261

Review 2.  Modeling and predicting clinical efficacy for drugs targeting the tumor milieu.

Authors:  Mallika Singh; Napoleone Ferrara
Journal:  Nat Biotechnol       Date:  2012-07-10       Impact factor: 54.908

3.  Optimizing the Sunitinib for cardio-toxicity and thyro-toxicity by scaffold hopping approach.

Authors:  Bhagyashri Chaudhari; Harun Patel; Snehal Thakar; Iqrar Ahmad; Deepali Bansode
Journal:  In Silico Pharmacol       Date:  2022-07-02
  3 in total

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