Shackelford David B, Vasquez Debbie S, Corbeil Jacqueline, Wu Shulin, Leblanc Mathias, Wu Chin-Lee, Vera David R, Shaw Reuben J
Dulbecco Center for Cancer Research, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 2009 Jul 7;106(27):11137-42. doi: 10.1073/pnas.0900465106. Epub 2009 Jun 18.
Peutz-Jeghers syndrome (PJS) is a familial cancer disorder due to inherited loss of function mutations in the LKB1/ STK11 serine/threonine kinase. PJS patients develop gastrointestinal hamartomas with 100% penetrance often in the second decade of life, and demonstrate an increased predisposition toward the development of a number of additional malignancies. Among mitogenic signaling pathways, the mammalian-target of rapamycin complex 1 (mTORC1) pathway is hyperactivated in tissues and tumors derived from LKB1-deficient mice. Consistent with a central role for mTORC1 in these tumors, rapamycin as a single agent results in a dramatic suppression of preexisting GI polyps in LKB1+/- mice. However, the key targets of mTORC1 in LKB1-deficient tumors remain unknown. We demonstrate here that these polyps, and LKB1- and AMPK-deficient mouse embryonic fibroblasts, show dramatic up-regulation of the HIF-1alpha transcription factor and its downstream transcriptional targets in an rapamycin-suppressible manner. The HIF-1alpha targets hexokinase II and Glut1 are up-regulated in these polyps, and using FDG-PET, we demonstrate that LKB1+/- mice show increased glucose utilization in focal regions of their GI tract corresponding to these gastrointestinal hamartomas. Importantly, we demonstrate that polyps from human Peutz-Jeghers patients similarly exhibit up-regulated mTORC1 signaling, HIF-1alpha, and GLUT1 levels. Furthermore, like HIF-1alpha and its target genes, the FDG-PET signal in the GI tract of these mice is abolished by rapamycin treatment. These findings suggest a number of therapeutic modalities for the treatment and detection of hamartomas in PJS patients, and potential for the screening and treatment of the 30% of sporadic human lung cancers bearing LKB1 mutations.
黑斑息肉综合征(PJS)是一种家族性癌症疾病,由LKB1/STK11丝氨酸/苏氨酸激酶的功能丧失性突变遗传所致。PJS患者通常在生命的第二个十年出现具有100%外显率的胃肠道错构瘤,并表现出对多种其他恶性肿瘤发生的易感性增加。在促有丝分裂信号通路中,雷帕霉素复合物1(mTORC1)通路在源自LKB1缺陷小鼠的组织和肿瘤中被过度激活。与mTORC1在这些肿瘤中的核心作用一致,雷帕霉素作为单一药物可显著抑制LKB1+/-小鼠中已有的胃肠道息肉。然而,mTORC1在LKB1缺陷肿瘤中的关键靶点仍然未知。我们在此证明,这些息肉以及LKB1和AMPK缺陷的小鼠胚胎成纤维细胞,以雷帕霉素可抑制的方式显示出HIF-1α转录因子及其下游转录靶点的显著上调。HIF-1α的靶点己糖激酶II和Glut1在这些息肉中上调,并且使用FDG-PET,我们证明LKB1+/-小鼠在其胃肠道对应于这些胃肠道错构瘤的局部区域显示出葡萄糖利用增加。重要的是,我们证明来自人类黑斑息肉病患者的息肉同样表现出mTORC1信号、HIF-1α和GLUT1水平上调。此外,与HIF-1α及其靶基因一样,这些小鼠胃肠道中的FDG-PET信号通过雷帕霉素治疗而消除。这些发现提示了多种治疗和检测PJS患者错构瘤的治疗方式,以及筛查和治疗30%携带LKB1突变的散发性人类肺癌的潜力。