BioMed Research International

BioMed Research International / 2015 / Article
Special Issue

Angiogenesis

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Editorial | Open Access

Volume 2015 |Article ID 135861 | https://doi.org/10.1155/2015/135861

Qiang Zhao, Zongjin Li, "Angiogenesis", BioMed Research International, vol. 2015, Article ID 135861, 2 pages, 2015. https://doi.org/10.1155/2015/135861

Angiogenesis

Received11 Feb 2015
Accepted11 Feb 2015
Published29 Mar 2015

The development of new blood vessels, termed as angiogenesis, is essential to embryonic growth and throughout life for physiological repair processes. The field of angiogenesis research was established approximately in 1970s by the Folkman hypothesis that tumor growth is angiogenesis-dependent [1]. In addition to the tumor growth, another promising field where angiogenesis has drawn attention as a critical target is cardiovascular diseases [2]. Therefore, inhibiting angiogenesis is a promising strategy for treating diseases like cancer, while promoting angiogenesis may benefit the ischemic diseases such as myocardial infarction. Molecular insights into these processes and new therapeutic approaches are therefore particularly promising tools to understand the underlying pathologies and expand the available therapeutic options in abnormal angiogenesis. This special issue on angiogenesis highlights recent advances in our understanding of the molecular and cellular mechanisms of neovascularization. The summary of this special issue could be found in Figure 1.

With more bioassays and preclinical experiments performed, progress in understanding the relationship between tumor growth and angiogenesis has created a new perspective on therapeutic angiogenesis. Metformin is one of the most efficacious and safe front-line antidiabetics for type 2 diabetes (T2D). Gao et al. provided an overview of metformin as potential anticancer treatment by inhibiting angiogenesis. Tumor angiogenesis also influenced tumor microenvironment and C. Liu et al. described that exogenous overexpression of ATF4 (activating transcription factor 4) may facilitate the recruitment of macrophages into tumor tissues and promote tumor angiogenesis. Though atherosclerosis will trigger ischemia diseases, a clearer prescription of angiogenesis accounting for the development of the plaque of atherosclerosis is well recognized. F. Vasuri et al. evaluated the relationship between the intraplaque angiogenesis and the clinical plaque instability. Furthermore, L. Wang et al. reviewed the antiangiogenesis effects of polymethoxyflavones (PMFs), which underline the important of traditional medicine for anticancer therapy.

Ischemic cardiovascular diseases are the major cause of mortality and morbidity, which appeals for more effort on the better and more useful treatments. Therapeutic angiogenesis with stem cell and biomaterial has appeared as a powerful option. B. Chiara et al. described the angiogenic properties of mesenchymal stem cells (MSCs) and further emphasized the role of SIRT1. D. Mao et al. reported the therapeutic effects of SKP (skin-derived precursor cell) in stroke by promoting neurogenesis and angiogenesis. Furthermore, K. Wang et al. developed hybrid PCL/gelatin fibrous scaffolds with sustained release of VEGF, which could enhance vascularization in vivo. D. P. Zankov et al. reviewed the involvement of actin cytoskeleton-associated junctional molecules in angiogenesis and lymphangiogenesis, which may present a new approach to angiogenic therapy.

In general, this special issue on angiogenesis covered both excessive angiogenesis and insufficient angiogenesis (Figure 1). Either the reports or the reviews on angiogenesis presented in this issue will provide a further understanding about the real role of angiogenesis in cardiovascular diseases or cancer.

Qiang Zhao
Zongjin Li

References

  1. J. Folkman, “Tumor angiogenesis: therapeutic implications,” The New England Journal of Medicine, vol. 285, no. 21, pp. 1182–1186, 1971. View at: Publisher Site | Google Scholar
  2. M. Huang, W. Du, Z. X. He, and Z. Li, “Molecular imaging of angiogenesis in cardiovascular diseases,” Journal of Molecular Biology and Molecular Imaging, vol. 1, no. 3, p. 6, 2014. View at: Google Scholar

Copyright © 2015 Qiang Zhao and Zongjin Li. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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