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• W1767051804 abstract "Pulmonary artery hypertension (PAH) is now considered to be a proliferative disorder characterised by unexplained proliferation of pulmonary artery smooth muscle cells (PA-SMCs) and pulmonary artery endothelial cells (PA-ECs). An abnormal phenotype of PA-SMCs and PA-ECs has been described in PAH and some analogies now appear between pulmonary vascular cells from patients with PAH and cancer cells. Such analogies are discussed here with respect to essential hallmarks of cancer cells and with the hope that new treatments targeted at one or more of these cancer cell abnormalities may be appropriate for PAH." @default.
• W1767051804 created "2016-06-24" @default.
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• W1767051804 date "2007-12-11" @default.
• W1767051804 modified "2023-09-25" @default.
• W1767051804 title "Lessons from oncology to understand and treat pulmonary hypertension" @default.
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• W1767051804 doi "https://doi.org/10.1111/j.1742-1241.2007.01618.x" @default.
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