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大肠癌组织中SOX4蛋白的表达变化及意义 被引量:1

Expression and significance of SOX4 protein in colorectal carcinoma
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摘要 目的观察SOX4蛋白在大肠癌组织中的表达变化,并探讨其意义。方法采用免疫组化SP法对大肠正常黏膜及原发大肠癌组织中的SOX4蛋白进行检测。结果 SOX4蛋白在大肠癌组织中的表达水平显著高于大肠正常黏膜组织(P<0.01);有淋巴结转移的大肠癌组织中SOX4蛋白表达水平明显高于无淋巴结转移者(P<0.01);SOX4蛋白表达水平与癌组织浸润肠壁深度有关(P<0.01),而与癌细胞分化程度无关(P>0.05)。结论SOX4蛋白在大肠癌组织中高表达,与大肠癌的浸润转移有关,可作为大肠癌发生发展的预测指标之一。 Objective To observe the changes of SOX4 protein expression in colorectal carcinoma(CRC) and investi- gate the significance. Methods The expression of SOX4 protein in normal colorectal mucosae and primary CRCs was de- tected using immunohistochemistry. Results The expression levels of SOX4 protein in CRC tissues were significantly high- er than those in normal colorectal mucosa tissues (P 〈 0.01 ). The expression of SOX4 protein in CRCs with lymph node metastasis was significantly higher than those without lymph node metastasis (P 〈 0.01 ). The SOX4 protein expression, showing no correlation with the differentiation of CRC ( P 〉 0.05 ), was positively correlated with the infiltrating depth of carcinomas (P 〈 0.01 ). Conclusion SOX4 protein, highly expressed in CRCs, is related to the infiltrating and metasta- sis of CRC and might be a valuable marker for the carcinogenesis and progression of CRC.
机构地区 南方医科大学
出处 《山东医药》 CAS 2013年第15期10-12,共3页 Shandong Medical Journal
基金 高等学校博士学科点专项科研基金资助项目(20094422120010) 广东省医学科研基金资助项目(A2010346) 南方医科大学基础医学院院长基金资助项目(JC0904)
关键词 大肠肿瘤 大肠癌 Y染色体性别决定区域 SOX基因 SOX4蛋白 colorectal neoplasms colorectal carcinoma sex-determining region of Y chromosome SRY-related HMG-box gene SOX4 protein
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  • 1Bowles J, Schepers G, Koopman P. Phylogeny of the SOX family of developmental transcription factors based on sequence and struc- tural indicators [ J ]. Dev Biol, 2000, 227 ( 2 ) : 239 -255.
  • 2Katoh M. Expression of human SOX7 in normal tissues and tumors [J]. Int J Mol Med, 2002, 9(4) :363-368.
  • 3Geijsen N, Uings IJ, Pals C, et al. Cytokine-specific transcription- al regulation through an IL-5Ralpha interacting protein [ J]. Sci- ence, 2001,293(5532):1136-1138.
  • 4Hur W, Rhim H, Jung CK, et al. SOX4 overexpression regulates the p53-mediated apoptosis in hepatocellular carcinoma: clinical implication and funqtianal analysis in vitro [ J]. Carcinogenesis, 2010, 31 (7) : 1298-1307.
  • 5Aue G, Du Y, Cleveland SM, et al. SOX4 cooperates with PU. 1 haploinsufficiency in murine myeloid leukemia[ J]. Blood, 2011, 118 (17) :4674-4681.
  • 6Gunes S, Yegin Z, Sullu Y, et al. SOX4 expression levels in urothelial bladder carcinoma [ J]. Pathol Res Pract, 2011, 207 (7) :423-427.
  • 7Andersen CL, Christensen LL, Thorsen K, et al. Dysregulation of the transcription factors SOX4, CBFB and SMARCC1 correlates with outcome of colorectal cancer [ J]. Br J Cancer, 2009, 100 (3) :511-523.
  • 8Shen R, Pan S, Qi S, et al. Epigenetic repression of microRNA- 129-2 leads to overexpression of SOX4 in gastric cancer[ J]. Bio- chem Biophys Res Commun, 2010,394 (4) : 1047-1052.
  • 9Huang YW, Liu JC, Deatherage DE, et al. Epigenetic repression of microRNA-129-2 leads to overexpression of SOX4 oncogene in endometrial cancer [ J ]. Cancer Res, 2009,69 ( 23 ) :9038 -9046.
  • 10Lin B, Madan A, Yoon JG, et al. Massively parallel signature se- quencing and bioinformatics analysis identifies up-regulation of TG- FBI and SOX4 in human glioblastoma[ J]. PLoS One, 2010,5 (4) :10210.

二级参考文献7

  • 1陈伟,林叶,侯宝华,区金锐,简志祥.规范化网络信息系统支持的肝癌标本库建立探讨[J].实用医学杂志,2007,23(6):826-827. 被引量:22
  • 2Dong C, Wilhelm D, Koopman P. Sox genes and cancer [ J ]. Cytognet Genome Res, 2004, 105(2-4):442-7.
  • 3Wilson ME, Yang KY, Kalousova A, et al. The HMG box transcription factor SoX4 contributes to the development of the endocrine pancreas [ J ]. Diabetes, 2005, 54( 12): 3402-9.
  • 4Sinner D, Jennifer J, Kordich S, et al. Sox17 and Sox4 differentially regulate β- catcnin/T- cell factor activity and proliferation of colon carcinoma cells [ J ]. Mol Cellular Biol, 2007, 27(22): 7802-15.
  • 5Ahn SG, Kim HS, Jeong SW, et al. Sox-4 is a positive regulator of Hep3B and HepG2 cells' apoptosis induced by prostaglandin (PG)A (2) and delta(12)-PGJ(2)[J]. Exp Moi Med, 2002, 34(3): 243-9.
  • 6Liu P, Ramachandran S, Seyed MA, et al. Sex-determining region Y box 4 is a transforming oncogene in human prostate cancer cells [J ]. Cancer Res, 2006, 66(8): 4011-9.
  • 7Liao YL, Sun YM, Chau GY, et al. Identification of SOX4 target genes using phylogenetic footprinting-based prediction from expression microarrays suggests that overexpression of SOX4 potentiates metastasis in hepatocellular carcinoma [J]. Oncogene, 2008, 27: 5578-89.

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