Literature DB >> 24919955

Elevated expression of AKT2 correlates with disease severity and poor prognosis in human osteosarcoma.

Yalong Zhu1, Jianhua Zhou1, Ying Ji1, Baoqing Yu1.   

Abstract

Members of AKT kinase family are central modulators in numerous signaling cascades, which regulate metabolism, cell proliferation, survival and growth. Previously, the knockdown of AKT2 expression has been demonstrated to enhance the efficacy of chemotherapy in patients with osteosarcoma. However, it is currently unknown whether the aberrant expression of AKT2 has relevance to the progression of osteosarcoma. The aim of the present study was to investigate the clinicopathological and prognostic value of AKT2 in osteosarcoma. Formalin-fixed paraffin embedded osteosarcoma and self-paired non-cancerous bone tissue samples were obtained from 126 patients with osteosarcomas. AKT2 expression was detected by an immunohistochemistry assay. Patient survival rates were determined by the Kaplan-Meier method and log-rank test. Cox regression was adopted for multivariate analysis of the prognostic factors to examine the effect of AKT on event-free survival and overall survival in patients with osteosarcomas. AKT2 expression in osteosarcoma tissues was significantly higher than that in non-cancerous bone tissues (immunostaining score, 6.39±1.62 vs. 3.46±1.03; P<0.001). In addition, the elevated expression of AKT2 protein was significantly associated with positive recurrence (P=0.023), the presence of metastasis (P=0.006) and poor response to chemotherapy (P=0.015). Furthermore, patients with high AKT2 expression had significantly shorter event-free survival (P<0.001) and overall survival times (P<0.001) than those with lower expression levels. Multivariate analysis further demonstrated that AKT2 expression (P=0.029 and 0.016, respectively), the status of recurrence (P=0.018 and 0.012, respectively) and metastasis (P=0.020 and 0.015, respectively), and the response to chemotherapy (P=0.011 and 0.008, respectively) were all independent prognostic factors for event-free survival and overall survival time. To the best of our knowledge, these data have supported the findings for the first time, that the elevated expression of AKT2 may be associated with aggressive clinical behavior and poor outcome in patients with osteosarcomas. Therefore, AKT2 may be a candidate marker of unfavorable prognosis in osteosarcoma.

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Year:  2014        PMID: 24919955     DOI: 10.3892/mmr.2014.2314

Source DB:  PubMed          Journal:  Mol Med Rep        ISSN: 1791-2997            Impact factor:   2.952


  10 in total

1.  Analyzing the Interactions of mRNAs and ncRNAs to Predict Competing Endogenous RNA Networks in Osteosarcoma Chemo-Resistance.

Authors:  Kun-Peng Zhu; Chun-Lin Zhang; Xiao-Long Ma; Jian-Ping Hu; Tao Cai; Lei Zhang
Journal:  Mol Ther       Date:  2019-01-07       Impact factor: 11.454

2.  Receptor activator of nuclear factor κB expression is a prognostic factor in human osteosarcoma.

Authors:  Klemens Trieb; Reinhard Windhager
Journal:  Oncol Lett       Date:  2015-07-14       Impact factor: 2.967

3.  A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis.

Authors:  Branden S Moriarity; George M Otto; Eric P Rahrmann; Susan K Rathe; Natalie K Wolf; Madison T Weg; Luke A Manlove; Rebecca S LaRue; Nuri A Temiz; Sam D Molyneux; Kwangmin Choi; Kevin J Holly; Aaron L Sarver; Milcah C Scott; Colleen L Forster; Jaime F Modiano; Chand Khanna; Stephen M Hewitt; Rama Khokha; Yi Yang; Richard Gorlick; Michael A Dyer; David A Largaespada
Journal:  Nat Genet       Date:  2015-05-11       Impact factor: 38.330

4.  RNA sequencing identifies gene expression profile changes associated with β-estradiol treatment in U2OS osteosarcoma cells.

Authors:  Bin Chen; Zude Liu; Jidong Zhang; Hantao Wang; Bo Yu
Journal:  Onco Targets Ther       Date:  2017-07-11       Impact factor: 4.147

5.  A 2D-QSAR and Grid-Independent Molecular Descriptor (GRIND) Analysis of Quinoline-Type Inhibitors of Akt2: Exploration of the Binding Mode in the Pleckstrin Homology (PH) Domain.

Authors:  Noreen Akhtar; Ishrat Jabeen
Journal:  PLoS One       Date:  2016-12-30       Impact factor: 3.240

6.  Downregulation of Homeobox B7 Inhibits the Tumorigenesis and Progression of Osteosarcoma.

Authors:  Lei Yang; Fei Xie; Shuangqing Li
Journal:  Oncol Res       Date:  2016-11-08       Impact factor: 5.574

7.  Profiling of three H3F3A-mutated and denosumab-treated giant cell tumors of bone points to diverging pathways during progression and malignant transformation.

Authors:  Marc Hasenfratz; Kevin Mellert; Ralf Marienfeld; Alexandra von Baer; Markus Schultheiss; P D Roitman; L A Aponte-Tinao; Burkhard Lehner; Peter Möller; Gunhild Mechtersheimer; Thomas F E Barth
Journal:  Sci Rep       Date:  2021-03-11       Impact factor: 4.379

8.  RLN2 Is a Positive Regulator of AKT-2-Induced Gene Expression Required for Osteosarcoma Cells Invasion and Chemoresistance.

Authors:  Jinfeng Ma; Hai Huang; Zenggang Han; Changzheng Zhu; Bin Yue
Journal:  Biomed Res Int       Date:  2015-07-01       Impact factor: 3.411

9.  MiR-200c regulates tumor growth and chemosensitivity to cisplatin in osteosarcoma by targeting AKT2.

Authors:  Yang Liu; Shu-Tao Zhu; Xiao Wang; Jun Deng; Wei-Hua Li; Peng Zhang; Bing-Shan Liu
Journal:  Sci Rep       Date:  2017-10-19       Impact factor: 4.379

10.  AKT2 drives cancer progression and is negatively modulated by miR-124 in human lung adenocarcinoma.

Authors:  Ting Liu; Jianjie Zhu; Wenwen Du; Weiwei Ning; Yang Zhang; Yuanyuan Zeng; Zeyi Liu; Jian-An Huang
Journal:  Respir Res       Date:  2020-09-01
  10 in total

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