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New therapies for prostate cancer?

机译:前列腺癌的新疗法?

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Worldwide, over 600,000 men are diagnosed with prostate cancer each year and prostate cancer remains an important cause of morbidity and mortality. Despite recent advances in the early detection of prostate cancer and less invasive radiotherapies, such as cyberknife, prostate cancer remains a significant health risk in men. Mechanistically, the increased expression of proto-oncogenes, and the activation of cell cycle regulatory genes, in combination with compromised tumor suppressor activity are as common in prostate cancer as it is in other malignancies, such as breast cancer. Major differences exist, however, in the ability to clinically intervene. Loss-of-function events have been demonstrated to occur in prostate cancer for p27~(KIPI), p16~(INK4A) and the reti-noblastoma protein, Rb. Perhaps the most frequently compromised prostate cancer tumor suppressor gene is the lipid phosphatase and inhibitor of P13 kinase signaling, PTEN.
机译:全世界每年有600,000多名男性被诊断出患有前列腺癌,而前列腺癌仍然是发病率和死亡率的重要原因。尽管在早期检测前列腺癌和侵入性较小的放射疗法如射波刀方面取得了最新进展,但是前列腺癌仍然是男性的重大健康风险。从机制上讲,原癌基因表达的增加和细胞周期调控基因的激活与肿瘤抑制活性的降低在前列腺癌中和在其他恶性肿瘤(如乳腺癌)中一样普遍。但是,主要的差异在于临床干预的能力。已经证实在前列腺癌中p27〜(KIPI),p16〜(INK4A)和视网膜母细胞瘤蛋白Rb发生功能丧失事件。也许最常见的前列腺癌肿瘤抑制基因是脂质磷酸酶和P13激酶信号传导抑制剂PTEN。

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