Expression of E-cadherin and β1-integrin mRNA in endometrial cancer

被引:0
作者
Wojcik-Krowiranda, Katarzyna [1 ]
Forma, Ewa [2 ]
Zaczek, Agnieszka [2 ]
Brys, Magdalena [2 ]
Anna, Magdalena Krzeslak [2 ]
Bienkiewicz, Andrzej [1 ]
机构
[1] Med Univ Lodz, Dept Gynecol Oncol, Lodz, Poland
[2] Univ Lodz, Dept Cytobiochem, PL-90131 Lodz, Poland
关键词
molecular marker; E-cadherin; beta; 1-integrin; CDH1; ITGB1; endometrial carcinoma; gene expression; INTEGRIN; INVASION;
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: The metastatic ability of tumors is characteristic for malignant neoplasms and constitutes the main cause of therapeutics failures. Metastasis formation involves the sequence of processes such as proteolytic degradation of the basement membrane, migration, intravasation, extravasation, proliferation and angiogenesis. Cadherins and integrins are groups of proteins directly involved in these processes. In the present study we analyzed the mRNA expression of CDH1 and ITGB1 genes by real-time polymerase chain reaction (RT-PCR). The study included 106 endometrial carcinomas. CDH1 and ITGB1 mRNA expression was found in all of the studied samples. Generally, the CDH1 and ITGB1 mRNA expression was significantly higher in well-differentiated rather than poorly differentiated tumors. Materials and methods: The mRNA expression levels of CDH1 and ITGB1 in series of 83 samples of endometrial carcinoma were studied by real time RT-PCR method. Statistical analysis of the obtained results was performed. Results: CDH1 and ITGB1 gene expression was observed in all examined tissues and was correlated with cancer malignancy (G). In high grade malignant tumors (G1), CDH1 and ITGB1 gene expression was the highest, in G2 and G3 tumors the expression of both genes was gradually lowering. Moreover, the statistically significant correlation between CDH1 and ITGB1 gene expression was observed. (Spearman test, r=0.29, p<0.01). Conclusion: CDH1 and ITGB1 mRNA expression seems to be an important marker of cancer progression and metastases in endometrial malignant tumors.
引用
收藏
页码:910 / 914
页数:5
相关论文
共 50 条
[41]   Targeting E-cadherin expression with small molecules for digestive cancer treatment [J].
Song, Yizuo ;
Ye, Miaomiao ;
Zhou, Junhan ;
Wang, Zhiwei ;
Zhu, Xueqiong .
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2019, 11 (07) :3932-3944
[42]   Expression of E-cadherin and catenins in early gastric cancer [J].
Joo, YE ;
Rew, JS ;
Choi, SK ;
Bom, HS ;
Park, CS ;
Kim, SJ .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2002, 35 (01) :35-42
[43]   EXPRESSION OF E-CADHERIN/CATENIN COMPLEX IN BREAST CANCER [J].
刘臻 ;
崔东旭 ;
刘宝林 ;
张小薄 ;
马文锋 ;
张强 .
Chinese Journal of Cancer Research, 2006, (04) :299-305
[44]   Relationship between LSD1 expression and E-cadherin expression in prostate cancer [J].
Min Wang ;
Xiuheng Liu ;
Guanjun Jiang ;
Hui Chen ;
Jia Guo ;
Xiaodong Weng .
International Urology and Nephrology, 2015, 47 :485-490
[45]   E-cadherin expression in thymomas [J].
Yang, WI ;
Yang, KM ;
Hong, SW ;
Kim, KD .
YONSEI MEDICAL JOURNAL, 1998, 39 (01) :37-44
[46]   E-cadherin expression as a differentiation marker in gastric cancer [J].
Karayiannakis, AJ ;
Syrigos, KN ;
Chatzigianni, E ;
Papanikolaou, S ;
Karatzas, G .
HEPATO-GASTROENTEROLOGY, 1998, 45 (24) :2437-2442
[47]   Expression of E-cadherin in angiomyolipoma [J].
Wang, Zhen ;
Gong, Qixing ;
Fan, Qinhe .
HUMAN PATHOLOGY, 2012, 43 (12) :2348-2353
[48]   Contactin-1 Reduces E-Cadherin Expression Via Activating AKT in Lung Cancer [J].
Yan, Judy ;
Wong, Nicholas ;
Hung, Claudia ;
Chen, Wendy Xin-Yi ;
Tang, Damu .
PLOS ONE, 2013, 8 (05)
[49]   APC, β-catenin, and E-cadherin and the development of recurrent endometrial carcinoma [J].
Pijnenborg, JMA ;
Kisters, N ;
Van Engeland, M ;
Dunselman, GAJ ;
De Haan, J ;
De Goeij, AFPM ;
Groothuis, PG .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2004, 14 (05) :947-956
[50]   E-Cadherin Expression in Endometrial Malignancies: Comparison between Endometrioid and Non-endometrioid Carcinomas [J].
Yalta, T. ;
Atay, L. ;
Atalay, F. ;
Caydere, M. ;
Gonultas, M. ;
Ustun, H. .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2009, 37 (01) :163-168