Majumder Pradip K, Sellers William R
Department of Medical Oncology, Dana Farber Cancer Institute, Boston, MA 02115, USA.
Oncogene. 2005 Nov 14;24(50):7465-74. doi: 10.1038/sj.onc.1209096.
Prostate cancer remains a major cause of cancer-related mortality. Genetic clues to the molecular pathways driving the most aggressive forms of prostate cancer have been limited. Genetic inactivation of PTEN through either gene deletion or point mutation is reasonably common in metastatic prostate cancer and the resulting activation of phosphoinostide 3-kinase, AKT and mTOR provides a major therapeutic opportunity in this disease as mTOR inhibitors, HSP90 inhibitors and PI3K inhibitors begin to enter clinical development.
前列腺癌仍然是癌症相关死亡的主要原因。驱动最具侵袭性前列腺癌形式的分子途径的遗传线索一直有限。通过基因缺失或点突变导致的PTEN基因失活在转移性前列腺癌中相当常见,由此导致的磷酸肌醇3激酶、AKT和mTOR的激活为这种疾病提供了一个主要的治疗机会,因为mTOR抑制剂、HSP90抑制剂和PI3K抑制剂开始进入临床开发阶段。