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  • Case Report   
  • J Cell Mol Pharmacol 2022, Vol 6(3)Vol 6(3)
  • DOI: 10.4172/jcmp.1000125

The Function of VEGF in Systemic Disease and Cancer Metastasis

Yihai Cao*
Department of Microbiology, Tumor and Cell Biology, Biomedicum, Karolinska Institute, 171 77 Stockholm, Sweden
*Corresponding Author : Yihai Cao, Innovation Center for Molecular Target New Drug Study, Hengyang Medical College, Institution of Pathogenic Biology, University of South China, Hengyang, China, Email: yiuwu@sina.com

Received Date: Jun 04, 2022 / Published Date: Jun 28, 2022

Abstract

Metastasis is the leading cause of cancer-associated mortality and the underlying mechanisms of cancer metastasis remain elusive. Both blood and lymphatic vasculatures are essential structures for mediating distal metastasis. The vasculature plays multiple functions, including accelerating tumor growth, sustaining the tumor microenvironment, supplying growth and invasive signals, promoting metastasis, and causing cancer-associated systemic disease. VEGF is one of the key angiogenic factors in tumors and participates in the initial stage of tumor development, progression and metastasis. Consequently, VEGF and its receptor-mediated signaling pathways have become one of the most important therapeutic targets for treating various cancers [1-15]. Today, anti-VEGFbased antiangiogenic drugs (AADs) are widely used in the clinic for treating different types of cancer in human patients. Despite nearly 20-year clinical experience with AADs, the impact of these drugs on cancer metastasis and systemic disease remains largely unknown. In this review article, we focus our discussion on tumor VEGF in cancer metastasis and systemic disease and mechanisms underlying AADs in clinical benefits.

Citation: Cao Y (2022) The Function of VEGF in Systemic Disease and Cancer Metastasis. J Cell Mol Pharmacol 6: 125. Doi: 10.4172/jcmp.1000125

Copyright: © 2022 Cao Y. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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