SGK3 is associated with estrogen receptor expression in breast cancer

被引:25
作者
Xu, Jun [1 ,2 ,3 ]
Wan, Ma [1 ]
He, Quanyuan [1 ]
Bassett, Roland L., Jr. [4 ]
Fu, Xiaoyong [5 ]
Chen, Albert C. [5 ]
Shi, Fengtao [1 ]
Creighton, Chad J. [3 ]
Schiff, Rachel [3 ,5 ]
Huo, Lei [6 ]
Liu, Dan [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Verna & Marrs Mclean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Cell Based Assay Screening Core, Houston, TX 77030 USA
[3] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[5] Baylor Coll Med, Lester & Sue Smith Breast Ctr, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
SGK3; CISK; Estrogen receptor; Breast cancer; Immunohistochemistry; PI; 3-kinase; AKT ACTIVATION; GENE; MUTATIONS; PATHWAY; GROWTH; PTEN; RESISTANCE; BAD; PHOSPHORYLATION; SUSCEPTIBILITY;
D O I
10.1007/s10549-012-2081-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
While breast cancer mortality rate has seen a steady decline in the last few decades, advances in better treatment and diagnostic tools remain important as we come into the age of personalized therapy. In this report, we describe our studies of SGK3's role in breast cancer. SGK3 (also known as CISK) is a member of the AGC family of kinases. Our previous work indicates that SGK3 functions downstream of the PI 3-kinase cascade and shares molecular and biochemical similarities with Akt. Here, we show that SGK3 expression is linked to estrogen receptor (ER) both in breast caner cell lines and in primary tumor samples. Our analysis also indicated a positive correlation between SGK3 expression and tumor prognosis. Importantly, our immunochemistry analysis of human tumor samples established a clinical link between SGK3 expression and ER+ tumors. These findings implicate SGK3 as an additional component to a complex and heterogeneous disease, and point to the potential benefits of incorporating SGK3 into the process of breast cancer diagnosis and treatment.
引用
收藏
页码:531 / 541
页数:11
相关论文
共 66 条
  • [1] Immunohistochemical determination of oestrogen receptor: Comparison of different methods of assessment of staining and correlation with clinical outcome of breast cancer patients
    Barnes, DM
    Harris, WH
    Smith, P
    Millis, RR
    Rubens, RD
    [J]. BRITISH JOURNAL OF CANCER, 1996, 74 (09) : 1445 - 1451
  • [2] A transforming mutation in the pleckstrin homology domain of AKT1 in cancer
    Carpten, John D.
    Faber, Andrew L.
    Horn, Candice
    Donoho, Gregory P.
    Briggs, Stephen L.
    Robbins, Christiane M.
    Hostetter, Galen
    Boguslawski, Sophie
    Moses, Tracy Y.
    Savage, Stephanie
    Uhlik, Mark
    Lin, Aimin
    Du, Jian
    Qian, Yue-Wei
    Zeckner, Douglas J.
    Tucker-Kellogg, Greg
    Touchman, Jeffrey
    Patel, Ketan
    Mousses, Spyro
    Bittner, Michael
    Schevitz, Richard
    Lai, Mei-Huei T.
    Blanchard, Kerry L.
    Thomas, James E.
    [J]. NATURE, 2007, 448 (7152) : 439 - U1
  • [3] The PTEN-PI3K pathway: of feedbacks and cross-talks
    Carracedo, A.
    Pandolfi, P. P.
    [J]. ONCOGENE, 2008, 27 (41) : 5527 - 5541
  • [4] Chen Wong L., 2005, Current Medicinal Chemistry - Anti-Cancer Agents, V5, P575, DOI 10.2174/156801105774574649
  • [5] A gene transcription signature of the Akt/mTOR pathway in clinical breast tumors
    Creighton, C. J.
    [J]. ONCOGENE, 2007, 26 (32) : 4648 - 4655
  • [6] Development of resistance to targeted therapies transforms the clinically associated molecular profile subtype of breast tumor xenografts
    Creighton, Chad J.
    Massarweh, Suleiman
    Huang, Shixia
    Tsimelzon, Anna
    Hilsenbeck, Susan G.
    Osborne, C. Kent
    Shou, Jiang
    Malorni, Luca
    Schiff, Rachel
    [J]. CANCER RESEARCH, 2008, 68 (18) : 7493 - 7501
  • [7] Genes regulated by estrogen in breast tumor cells in vitro are similarly regulated in vivo in tumor xenografts and human breast tumors
    Creighton, Chad J.
    Cordero, Kevin E.
    Larios, Jose M.
    Miller, Rebecca S.
    D Johnson, Michael
    Chinnaiyan, Arul M.
    Lippman, Marc E.
    Rae, James M.
    [J]. GENOME BIOLOGY, 2006, 7 (04)
  • [8] ERM-mediated genetic screens in mammalian cells
    Dan Liu
    Zhou Songyang
    [J]. PROGRAMMED CELL DEATH, THE BIOLOGY AND THERAPEUTIC IMPLICATIONS OF CELL DEATH, PART B, 2008, 446 : 409 - 419
  • [9] Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
    Datta, SR
    Dudek, H
    Tao, X
    Masters, S
    Fu, HA
    Gotoh, Y
    Greenberg, ME
    [J]. CELL, 1997, 91 (02) : 231 - 241
  • [10] delPeso L, 1997, SCIENCE, V278, P687