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Mutations of proto-oncogenes will normally modify their normal expression and activity and they can be transformed to oncogenes via mutation. This can lead the cell to proliferate abnormally. Tumour suppressor gene (TSG) another important gene that regulates the normal cell growth and mitosis also plays a significant role in cancer formation. In cases of cellular stress or DNA damage the TSG will suppress normal function and promote cell cycle arrest to allow enough time for repair and to prevent mutations from passing to new cells. However if the TSG itself has been mutated the original functions of it can be switched off and DNA damage without repair may lead to mutation.
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- Thus the positive links between p53 and its effector gene p21 lead to binding of p21 to Cyclin-Cdks complexes which in turn inhibit the cells in G1 phase (Morgan 2007)
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- Effect of MSE and MIT on the cell cycle distribution 4
- P53 was thought to be a crucial component in the cell cycle control systems (Pellegata et al 1996)
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To my knowledge this study is the first to assess cytotoxicity potential of MSE and MIT. MIT is believed to be a major contributor to the analgesic effects of this plant. Since the potential toxicity of this plant is yet to be elucidated I am aiming to initiate toxicology research of this plant using in vitro studies to investigate the possible mechanisms best site buy kratom colbert involved. The sub-objectives are to be: 1.
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