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Recent developments in the regulation of the angiogenic switch by cellular stress factors in tumors
Abstract
Angiogenesis in tumors is controlled by the so-called 'angiogenic switch' which allows the passage from low invasive and poorly vascularized tumors to highly invasive and angiogenic tumors. A number of cellular stress factors such as hypoxia, nutrient deprivation or inducers of reactive oxygen species (ROS) are important stimuli of angiogenic signalling. The HIF system plays a significant role in several of these effects and the molecular mechanisms of its regulation have recently been characterized. In addition, HIF-independent mechanisms have been described which involved number of other molecules and transcription factors such as nuclear factor-(kappa)B (NF-(kappa)B) and p53. p53 is an important intracellular mediator of the stress response and is now also recognized as a modifier of the angiogenic response. p53 may interact with the HIF system but may also have direct effects on angiogenesis regulators or interfere with translation mechanisms of angiogenesis factors.
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“In these rats, biweekly phlebotomy was probably not sufficient to attenuate the tumor progression because a low level of oxidative stress might activate cellular proliferation, angiogenesis, and metastasis in tumors.38, 39”
From Phlebotomy as a preventive measure for crocidolite-induced mesothelioma in male rats (2018) · cites this paper as [39]
In the citing paper
“a low level of oxidative stress might activate cellular proliferation, angiogenesis, and metastasis in tumors.38, 39”
From Phlebotomy as a preventive measure for crocidolite-induced mesothelioma in male rats (2018) · cites this paper as [39]
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- Authors
- North, S., Moenner, M., & Bikfalvi, A.
- Venue
- Cancer Letters
- Publisher
- Elsevier BV
- Published
- 2005-01
- Volume
- 218
- Issue
- 1
- Pages
- 1-14
- ISSN
- 0304-3835
- Cited by
- 113
- References
- 13
- Language
- en
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