Estrogen receptor-β expression in human laryngeal carcinoma: Correlation with the expression of epithelial-mesenchymal transition specific biomarkers

被引:27
|
作者
Goulioumis, Anastasios K. [1 ,4 ]
Fuxe, Jonas [4 ]
Varakis, John [1 ]
Repanti, Maria [3 ]
Goumas, Panos [2 ]
Papadaki, Helen [1 ]
机构
[1] Univ Patras, Dept Anat, Sch Med, Patras 26500, Greece
[2] Univ Patras, Dept Otorhinolaryngol Head & Neck Surg, Sch Med, Patras 26500, Greece
[3] Agios Andreas Gen Hosp Patras, Dept Pathol, Patras, Greece
[4] Karolinska Inst, Dept Cell & Mol Biol, Stockholm, Sweden
关键词
estrogen receptor-beta (ER-beta); E-cadherin; beta-catenin; vimentin; laryngeal carcinoma; HUMAN BREAST-CANCER; E-CADHERIN; ALPHA; WNT; SNAIL;
D O I
10.3892/or_00000537
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Laryngeal carcinoma is a malignancy of the respiratory tract with a significantly higher male to female ratio, suggesting involvement of gender-depended factors in the pathogenesis. Estrogen influences the pathological processes of hormone-dependent cancers, such as breast, prostate and ovarian cancers, through its receptors, estrogen receptor-alpha (ER-alpha) and -beta (ER-beta). While ER-alpha promotes cell proliferation, recent studies indicate that ER-alpha is protective against carcinoma progression into an invasive state. However, it is unclear whether ER-beta plays a role in laryngeal cancer. In the present study we examined the expression of ER-beta in 80 invasive human squamous laryngeal carcinomas by immunohistochemistry and correlated ER-beta expression with markers of epithelial-mesenchymal transition (EMT). ER-beta was expressed in 83% of tumour specimens where it was localized in the nuclei of tumour cells. The expression of ER-beta correlated positively with the maintenance of Ecadherin and beta-catenin at cell junctions and negatively with the loss of E-cadherin, nuclear translocation of beta-catenin and increased TNM stage. We concluded that estrogen receptor beta expression is documented in laryngeal cancer indicating a possible role in the pathogenesis of this malignancy. It is suggested that ER-beta could protect tumour cells from acquiring aggressive EMT features such as E-cadherin downregulation and nuclear beta-catenin activation.
引用
收藏
页码:1063 / 1068
页数:6
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