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FOXA2在肝细胞癌中的临床意义及其与E-cadherin的相关性 被引量:4

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摘要 目的探讨检测FOXA2在肝细胞癌(HCC)中的临床意义及其与E-cadherin的相关性分析。方法采用免疫组织化学染色检测78例原发性HCC及对应癌旁组织中FOXA2和E-cadherin蛋白的表达情况,分析FOXA2蛋白表达与HCC不同临床病理特征的相关性以及其与E-cadherin蛋白表达相关性。结果 FOXA2和E-cadherin蛋白在HCC组织中的阳性表达率为44.9%(35/78)和52.6%(41/78),而对应癌旁组织中两者表达率为71.8%(56/78)和74.4%(58/78),差异具有统计学意义(χ2=11.631,P=0.001;χ2=7.989,P=0.005)。HCC组织中FOXA2与E-cadherin蛋白表达呈显著正相关(r=0.715,P=0.015)。FOXA2蛋白表达与肿瘤数目(χ2=5.552,P=0.018)、血管侵犯(χ2=9.329,P=0.002)和TNM分期(χ2=6.479,P=0.011)有关。结论 HCC组织中FOXA2蛋白表达缺失并与恶性临床病理特征密切相关,另外FOXA2与E-cadherin蛋白表达显著正相关,提示FOXA2缺失可能促进EMT从而导致肿瘤进展。
出处 《中国老年学杂志》 CAS CSCD 北大核心 2014年第21期5987-5989,共3页 Chinese Journal of Gerontology
基金 广东省自然科学基金资助项目(10151051501000120)
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  • 1文卫,杨连粤,黄耿文,杨治力,刘合利,杨建青.TSP-1和VEGF在肝细胞癌新生血管生成中的作用[J].中华肝胆外科杂志,2005,11(1):17-19. 被引量:19
  • 2Hai-XiaQin,Ke-JunNan,GuangYang,ZhaoJing,Zhi-PingRuan,Chun-LiLi,RuiXu,HuiGuo,Chen-GuangSui,Yong-ChangWei.Expression and clinical significance of TAp73α, p53, PCNA and apoptosis in hepatocellular carcinoma[J].World Journal of Gastroenterology,2005,11(18):2709-2713. 被引量:12
  • 3王洪海,任宁,张辉,叶青海,孙惠川,王鲁,谭云山,钦伦秀.联合检测VEGF、PD-ECGF和PCNA表达预测肝细胞癌术后复发及预后[J].中国临床医学,2005,12(3):448-451. 被引量:7
  • 4王艳,朱波,陈正堂.LYVE-1在肿瘤淋巴管生成领域的研究[J].生命的化学,2005,25(4):314-316. 被引量:7
  • 5Moustakas A, Heldin CH. Signaling networks guiding epithelial-mesenchymal transitions during embryogenesis and cancer progression. Cancer Sci 2007; 98:1512-1520.
  • 6Tsuji q2, Ibaragi S, Hu GF. Epithelial-mesenchymal transition and cell cooperativity in metastasis. Cancer Res 2009; 69:7135-7139.
  • 7Thiery JP, Acloque H, Huang RY, Nieto MA. Epithelial-mes-enchymal transitions in development and disease. Cell 2009; 139:871-890.
  • 8Cannito S, Novo E, Di Bonzo LV, Busletta C, Colombatto S, Parola M. Epithelial-mesenchymal transition: from molecular mechanisms, redox regulation to implications in human health and disease. AntioxidRedox Signal 2010; 12:1383-1430.
  • 9Thiery JP, Sleeman JP. Complex networks orchestrate epithe-lial-mesenchymal transitions. Nat Rev Mol Cell Biol 2006; 7:131-142.
  • 10Huber MA, Kraut N, Beug H. Molecular requirements for epithelial-mesenchymal transition during tumor progression. Curr Opin Cell Bio12005; 17: 548-558.

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  • 1Shen N,Gong J,Wang Y,et al. Integrative genomic analy-sis identifies that SERPINA6-rsl998056 regulated byFOXA/ERalpha is associated with female hepatocellularcarcinoma[ J]. PLoS One,2014,9 (9) :el07246.
  • 2Smith-Vikos T, de Lencastre A, Inukai S, et al. MicroR-NAs mediate dietary-restriction-induced longevity throughPHA-4/F0XA and SKN-l/Nrf transcription factors [ J ].Curr Biol,2014,24( 19) :2238 -2246.
  • 3Gupta A, Yu X, Case T, et al. Mashl expression is in-duced in neuroendocrine prostate cancer upon the loss ofFoxa2[J] . Prostate,2013 ,73(6) :582-589.
  • 4Wang J,Zhu CP,Hu PF,et al. FOXA2 suppresses the me-tastasis of hepatocellular carcinoma partially through ma-trix metalloproteinase-9 inhibition [ J ]. Carcinogenesis,2014,35(11) :2576 -2583.
  • 5Zhang Z,Yang C,Gao W,et al. F0XA2 attenuates the ep-ithelial to mesenchymal transition by regulating the tran-scription of E-cadherin and ZEB2 in human breast cancer[J]. Cancer Lett,2015 ,361(2) :240 -250.
  • 6Alder 0, Cullum R, Lee S, et al. Hippo signaling influ-ences HNF4A and F0XA2 enhancer switching duringhepatocyte differentiation [ J ] ‘ Cell Rep ,2014,9 ( 1) : 261-271.
  • 7Bahar Halpern K, Vana T, Walker MD. Paradoxical roleof DNA methylation in activation of FoxA2 gene expres-sion during endoderm development [ J ]. J Biol Chem,2014,289(34) :23882 -23892.
  • 8Song Y,Washington MK,Crawford HC. Loss of FOXA1/2is essential for the epithelial-to-mesenchymal transitionin pancreatic cancer [ J ]. Cancer Res,2010,70 ( 5 ):2115 -2125.
  • 9Katoh M,Katoh M. Transcriptional regulation of WNT2Bbased on the balance of Hedgehog, Notch, BMP andWNT signals [ J ] . Int J Oncol,2009,34 (5 ) : 1411 -1415.
  • 10Yunneng Tang Guangwen Shu Xinwang Yuan Naihe Jing Jianguo Song.FOXA2 functions as a suppressor of tumor metastasis by inhibition of epithelial-to-mesenchymal transition in human lung cancers[J].Cell Research,2011,21(2):316-326. 被引量:27

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