Clinicopathological and prognostic significance of phosphorylated PRAS40 (Thr246) in breast cancer

被引:1
|
作者
Fu, Rongzhan [1 ]
Wu, Hongyan [1 ]
Yuan, Kai [1 ]
Zhang, Kun [1 ]
机构
[1] Shandong Univ, Affiliated Qianfoshan Hosp, Dept Breast & Thyroid Surg, Jinan 250014, Peoples R China
关键词
Biomarker; PI3K pathway; PRAS40; phosphorylation; targeted therapy; TARGETED THERAPY; PATHWAY; LIMITATIONS;
D O I
10.5372/1905-7415.0604.092
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Phosphorylation of proline-rich Akt substrate of 40 kilodaltons at Thr246 (p-PRAS40(Thr246)) is a novel identified specific and stable biomarker for predicting phosphatidylinositol 3-kinase (PI3K) pathway activation and AKT inhibitor sensitivity. Objectives: We investigated the expression of p-PRAS40(Thr246) in breast cancer, and their chnicopathological characteristics and prognostic significance. Methods: The expression of p-PRAS40(Thr246) was detected by immunohistochemistry in 117 invasive breast cancer tumors. Results: p-PRAS40(Thr246) was positive in 62 (53.0%) of 117 patients. p-PRAS40(Thr246) expression was significantly associated with late tumor stages and shorter survival, but not with other clincopathological characteristics. Furthermore, p-PRAS40(Thr246) was also an independent prognostic factor for invasive breast cancers. Conclusion: High prevalence of p-PRAS40(Thr246) overexpression and its clinical significance in breast cancer suggests that this subgroup might benefit from PI3K inhibitors. We proposed that the detection of p-PRAS40Thr246 in breast cancer tissues should be included in the future clinical practice to develop patient-tailored treatments.
引用
收藏
页码:573 / 577
页数:5
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