Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Division of Hematology-Oncology, Penn State Hershey Cancer Institute, 500 University Drive, Hershey, PA 17033; Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Department of Medical Oncology and Molecular Therapeutics Program, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111.
Department of Pathology, Penn State Milton S. Hershey Medical Center, 500 University Drive, Hershey, PA 17033.
Neoplasia. 2018 Mar;20(3):244-255. doi: 10.1016/j.neo.2018.01.004. Epub 2018 Feb 12.
Plk2 is a target of p53. Our previous studies demonstrated that with wild-type p53, Plk2 impacts mTOR signaling in the same manner as TSC1, and Plk2-deficient tumors grew larger than control. Other investigators have demonstrated that Plk2 phosphorylates mutant p53 in a positive feedback loop. We investigated Plk2's tumor suppressor functions in relationship to mTOR signaling. Archival specimens from 12 colorectal adenocarcinomas were stained for markers including Plk2, phosphorylated mTOR (serine 2448) and ribosomal S6 (Serine 235/236). We show that Plk2 is expressed in normal colon, with a punctate staining pattern in supranuclear cytoplasm. In colorectal adenocarcinoma, Plk2 demonstrates complete or partial loss of expression. Strong expression of phosphorylated mTOR is observed in the invasive front. Phosphorylated S6 expression partially correlates with phosphorylated mTOR expression but appears more diffuse in some cases. p53 and Ki67 expression is diffuse, in the subset of cases examined. In order to determine whether Plk2 is lost prior to the development of invasive cancer, 8 colon polyps from 6 patients were evaluated for Plk2 expression. All polyps are positive for Plk2. A Cancer Genome Atlas search identified Plk2 mutations to be infrequent in colorectal adenocarcinomas. Neither Plk2 methylation (in the gene body) nor copy number variations correlated with changes in mRNA expression levels. Loss of Plk2 expression along with accentuated expression of phosphorylated mTOR and phosphorylated S6 at the invasive front in some colorectal carcinomas is consistent with previous findings that an interaction between Plk2 and TSC1 / mTOR signaling molecules plays a role in tumor suppression. Plk2 protein expression is lost at the same stage in colorectal carcinogenesis as p53. The p53 dependence of Plk2 loss and tumor suppressor function in relationship to mTOR signaling may have therapeutic implications.
Plk2 是 p53 的一个靶点。我们之前的研究表明,在野生型 p53 存在的情况下,Plk2 对 mTOR 信号的影响与 TSC1 相同,而 Plk2 缺陷型肿瘤的生长速度比对照快。其他研究人员已经证明,Plk2 以正反馈环的方式磷酸化突变型 p53。我们研究了 Plk2 在 mTOR 信号通路中的肿瘤抑制功能。对 12 例结直肠腺癌的存档标本进行了 Plk2、磷酸化 mTOR(丝氨酸 2448)和核糖体 S6(丝氨酸 235/236)的标记物染色。我们表明,Plk2 在正常结肠中表达,在核上细胞质中呈现点状染色模式。在结直肠腺癌中,Plk2 表现为完全或部分缺失表达。在侵袭前沿观察到磷酸化 mTOR 的强表达。磷酸化 S6 的表达部分与磷酸化 mTOR 的表达相关,但在某些情况下更为弥散。在检查的病例亚组中,p53 和 Ki67 的表达呈弥漫性。为了确定 Plk2 是否在浸润性癌症发生之前丢失,对 6 名患者的 8 个结肠息肉进行了 Plk2 表达评估。所有息肉均为 Plk2 阳性。癌症基因组图谱搜索发现 Plk2 突变在结直肠腺癌中并不常见。Plk2 甲基化(基因内)和拷贝数变异均与 mRNA 表达水平的变化无关。在一些结直肠癌中,Plk2 表达的丢失伴随着侵袭前沿磷酸化 mTOR 和磷酸化 S6 的表达增强,这与 Plk2 与 TSC1/mTOR 信号分子之间的相互作用在肿瘤抑制中发挥作用的先前发现一致。Plk2 蛋白表达在结直肠癌发生过程中的同一阶段丢失。Plk2 缺失和 mTOR 信号通路中肿瘤抑制功能的 p53 依赖性可能具有治疗意义。