Comparative characteristics of the transcriptional activity of CDH1, CTNNB1, VEGFA genes and expression of proteins E-cadherin, beta-catenin and VEGFA, coded by these genes in metastatic and non-metastatic endometrioid endometrial carcinoma

被引:2
作者
Tumanskiy, V. A. [1 ,2 ,3 ]
Chepets, A. V. [3 ]
Kamyshnyi, A. M. [4 ]
机构
[1] Zaporizhzhia State Med Univ, Honorary Sci & Engn Worker Ukraine, Zaporizhzhia, Ukraine
[2] Zaporizhzhia State Med Univ, Sci Work, Zaporizhzhia, Ukraine
[3] Zaporizhzhia State Med Univ, Dept Pathol Anat & Forens Med, Zaporizhzhia, Ukraine
[4] Zaporizhzhia State Med Univ, Dept Microbiol Virol & Immunol, Zaporizhzhia, Ukraine
来源
PATHOLOGIA | 2016年 / 02期
关键词
Endometrial Neoplasms; Cadherins; beta Catenin; VEGFA protein; Human; Polymerase Chain Reaction; RNA; Messenger;
D O I
10.14739/2310-1237.2016.2.81328
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The violation of Wnt-signaling pathway and cyclic neoangiogenesis is early events in endometrial carcinogenesis. In this process an important role is played by epigenetic modifications and mutations of CDH1, CTNNB1, VEGFA genes, followed by expression violations of E-cadherin, beta-catenin, VEGFA encoded by them. The aim. To study the expression levels of mRNA of CDH1, CTNNB1, VEGFA genes and the expression levels of E-cadherin, beta-catenin, VEGFA in non-metastatic endometrioid endometrial carcinoma (EEC) and in EEC with metastases to regional lymph nodes. Materials and methods. Immunohistochemical study of invasive pT(1-4)N(0)M(x) endometrioid endometrial carcinoma (EEC) (n=56; age - 42-83 years), invasive pT(1-4)N(1-2)M(x) EEC (n=30; age - 48-79 years), samples of normal proliferative endometrium (PE) (n=30; age - 41-62 years) was performed. Molecular-genetic study of invasive pT(1-4)N(0)M(x) EEC (n=10; age - 45-67 years), invasive pT(1-4)N(1-2)M(x) EEC (n=10; age - 44-63 years), samples of PE (n=10; age - 46-59 years) was performed. Results. EEC is characterized by the lower mRNA expression level of CDH1 gene and by the higher mRNA expression levels of CTNNB1, VEGFA genes in comparison with the PE. E-cadherin expression level is 32.6 % lower in non-metastatic EEC and also is 58.10 % lower in metastatic EEC in comparison with the PE. beta-catenin expression level is 32.56 % lower in non-metastatic EEC and also is 58.11 % lower in metastatic EEC in comparison with the PE. VEGFA expression level is 27.72 % higher in non-metastatic EEC and also is 17.87 % higher in metastatic EEC in comparison with the PE. There is lower beta-catenin expression level in metastatic EEC in comparison with non-metastatic EEC. Non-metastatic and metastatic EEC is characterized by the direct medium connections between the mRNA expression levels of CTNNB1 and VEGFA genes (gamma=0.44), between the mRNA expression level of CTNNB1 gene and VEGFA expression level in the tumor (gamma=0.37). Conclusions. These changes contribute to tumor growth, invasion and metastasis.
引用
收藏
页码:13 / 18
页数:6
相关论文
共 22 条
[1]  
Chernobrovkina A. E., 2014, MEDLINE RU, V15, P649
[2]  
Dabbs DJ, 2010, DIAGNOSTIC IMMUNOHIS
[3]   Biomarkers as prognostic factors in endometrial cancer [J].
Dobrzycka, Bozena ;
Terlikowski, Slawomir J. .
FOLIA HISTOCHEMICA ET CYTOBIOLOGICA, 2010, 48 (03) :319-322
[4]  
Dobrzycka B, 2010, GINEKOL POL, V81, P422
[5]  
Gulyaeva L. F., 2012, BYULLETEN VOSTOCHNO, V3-1, P110
[6]  
Isaeva A. V., 2015, VESTNIK RAMN, V70, P475, DOI [10.15690/vramn.v70.i4.1415, DOI 10.15690/VRAMN.V70.I4.1415]
[7]  
Jia Sh., 2015, CANC GENETICS EPIGEN, V3, P1, DOI [10.5376/cge.2015.03.0003, DOI 10.5376/CGE.2015.03.0003]
[8]   Participation of WNT and β-Catenin in Physiological and Pathological Endometrial Changes: Association with Angiogenesis [J].
Kiewisz, Jolanta ;
Wasniewski, Tomasz ;
Kmiec, Zbigniew .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[9]   Molecular pathology of endometrial carcinoma: practical aspects from the diagnostic and therapeutic viewpoints [J].
Llobet, D. ;
Pallares, J. ;
Yeramian, A. ;
Santacana, M. ;
Eritja, N. ;
Velasco, A. ;
Dolcet, X. ;
Matias-Guiu, X. .
JOURNAL OF CLINICAL PATHOLOGY, 2009, 62 (09) :777-785
[10]  
MA XY, 2014, AM J MOL BIOL, V4, P134, DOI DOI 10.4236/AJMB.2014.43015