The cross-regulation between SOX15 and Wnt signaling pathway

被引:35
作者
Moradi, Ali [1 ]
Ghasemi, Faezeh [2 ,3 ]
Anvari, Kazem [4 ]
Hassanian, Seyed Mahdi [5 ,6 ]
Simab, Saeideh Ahmadi [4 ]
Ebrahimi, Safieh [6 ]
Hesari, Amirreza [1 ,2 ]
Forghanifard, Mohammad Mahdi [1 ]
Boroushaki, Mohammad Taher [7 ,8 ]
ShahidSales, Soodabeh [4 ]
Avan, Amir [5 ]
机构
[1] Islamic Azad Univ, Damghan Branch, Dept Biol, Damghan, Iran
[2] Mashhad Univ Med Sci, Mol Med Grp, Sch Med, Dept Modern Sci & Technol, Mashhad, Iran
[3] Arak Univ Med Sci, Fac Med, Dept Biotechnol, Arak, Iran
[4] Mashhad Univ Med Sci, Sch Med, Canc Res Ctr, Mashhad, Iran
[5] Mashhad Univ Med Sci, Sch Med, Metab Syndrome Res Ctr, Mashhad, Iran
[6] Mashhad Univ Med Sci, Sch Med, Dept Med Biochem, Mashhad, Iran
[7] Mashhad Univ Med Sci, Fac Med, Dept Pharmacol, Mashhad, Iran
[8] Mashhad Univ Med Sci, Fac Med, Pharmacol Res Ctr Med Plants, Mashhad, Iran
关键词
biomarker; cancer; Sox15; WNT; B-CATENIN pathway; BETA-CATENIN; CANCER; EXPRESSION; GENES; OVEREXPRESSION; PROLIFERATION; PROGNOSIS; CELLS;
D O I
10.1002/jcp.25802
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
WNT/B-CATENIN signaling pathway is one of the key dysregulated pathways in different tumor types, which regulate the expression of several genes involved in cell proliferation, differentiation, and survival. This pathway is being modulated by sex-determining region Y-box (SOX) family genes. The functions of these genes are suggested as tumor suppressor or oncogene. SOX genes transcribe a group of transcription factors that play important roles in embryonic development and carcinogenesis. Among them, SOX15 is recently been identified as a novel tumor suppressor in pancreatic and esophagus cancers with a potential role in modulating Wnt/b-catenin signaling. This report summarizes the current knowledge about Wnt/b-catenin signaling pathway and its cross talk with SOX15 with particular emphasis on the value of SOX gene expression as prognostic or predictive biomarker in cancer.
引用
收藏
页码:3221 / 3225
页数:5
相关论文
共 33 条
[1]
Acquisition of SOX transcription factor specificity through protein-protein interaction, modulation of Wnt signalling and post-translational modification [J].
Bernard, Pascal ;
Harley, Vincent R. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2010, 42 (03) :400-410
[2]
The SOX family of genes in cancer development: biological relevance and opportunities for therapy [J].
Castillo, Sandra D. ;
Sanchez-Cespedes, Montse .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2012, 16 (09) :903-919
[3]
The role of Wnt genes in vertebrate development [J].
Dickinson, Mary E. ;
McMahon, Andrew P. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1992, 2 (04) :562-566
[4]
Sox genes and cancer [J].
Dong, C ;
Wilhelm, D ;
Koopman, P .
CYTOGENETIC AND GENOME RESEARCH, 2004, 105 (2-4) :442-447
[5]
Wnt/β-catenin signaling in cancer stemness and malignant behavior [J].
Fodde, Riccardo ;
Brabletz, Thomas .
CURRENT OPINION IN CELL BIOLOGY, 2007, 19 (02) :150-158
[6]
Sox17, the canonical Wnt antagonist, is epigenetically inactivated by promoter methylation in human breast cancer [J].
Fu, De-Yuan ;
Wang, Zhi-Min ;
Chen, Li ;
Wang, Bei-Lan ;
Shen, Zhen-Zhou ;
Huang, Wei ;
Shao, Zhi-Ming .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 119 (03) :601-612
[7]
Focus Issue: Wnt and β-Catenin Signaling in Development and Disease [J].
Gough, Nancy R. .
SCIENCE SIGNALING, 2012, 5 (206)
[8]
Decreased expression of SOX6 confers a poor prognosis in hepatocellular carcinoma [J].
Guo, Xiaodong ;
Yang, Mei ;
Gu, Hao ;
Zhao, Jingmin ;
Zou, Lin .
CANCER EPIDEMIOLOGY, 2013, 37 (05) :732-736
[9]
Haruhiko A., 2004, GENE DEV, V18, P1072
[10]
Upregulation of sex-determining region Y-box 9 (SOX9) promotes cell proliferation and tumorigenicity in esophageal squamous cell carcinoma [J].
Hong, Yingcai ;
Chen, Wen ;
Du, Xiaojun ;
Ning, Huiwen ;
Chen, Huaisheng ;
Shi, Ruiqing ;
Lin, Shaolin ;
Xu, Rongyu ;
Zhu, Jinrong ;
Wu, Shu ;
Zhou, Haiyu .
ONCOTARGET, 2015, 6 (31) :31241-31254