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Energy metabolism and angiogenesis in atherosclerosis and cancer

Doktorsavhandling
Författare Matias Ekstrand
Datum för examination 2019-11-08
ISBN 978-91-7833-563-3
Förlag Göteborgs universitet
Publiceringsår 2019
Publicerad vid Institutionen för medicin, avdelningen för molekylär och klinisk medicin
Språk en
Länkar hdl.handle.net/2077/60788
Ämnesord Energy metabolism, Hypoxia, Reactive oxygen species, Intussusceptive angiogenesis
Ämneskategorier Kardiologi, Cancer och onkologi

Sammanfattning

Energy metabolism requires supply of glucose and oxygen. In atherosclerotic plaques and cancer tumors, there are local areas with mismatch in demand and supply of oxygen and nutrients. The resulting cellular energy imbalance may promote energy failure and stimulation of angiogenesis. In the first paper, energy metabolites were analyzed in human atherosclerotic plaques using high-resolution bioluminescence imaging. Advanced plaques were deficient in ATP and glucose, whereas lactate accumulated. ATP and glucose deficiency was most pronounced in macrophage-rich areas adjacent to the necrotic core. ATP depletion may promote necrotic core expansion and progression from stable to unstable plaques. In the second paper, reactive oxygen species (ROS) production was studied during the development of atherosclerosis in mice. Intracellular ROS levels increased before lesions were visible, suggesting that intracellular ROS promote initiation of atherosclerosis. In advanced atherosclerotic plaques, atorvastatin decreased ROS production in a lipid-lowering independent manner. The decrease in ROS may promote stabilization of plaques. In the third paper, intussusceptive angiogenesis (IA) was demonstrated in human, but not mouse, melanoma metastases. IA may contribute to the growth of human melanoma metastases and help explain the poor effect of current anti-angiogenic drugs targeted to classic sprouting angiogenesis. We further demonstrated that MMP inhibition blocks IA in vitro. In summary, this thesis provides evidence of energy deficiency in human atherosclerotic plaques, new insights into ROS distribution during atherosclerosis development, and finally, evidence of intussusceptive angiogenesis in human malignant melanoma metastases. These data may be used to further the research into better treatments of atherosclerosis and cancer.

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