Oueslati Mohamed, Bettaieb Ilhem, Ben Younes Ridha, Gamoudi Amor, Rahal Khaled, Oueslati Ridha
Unit of Immunology, Environmental Microbiology and Carcinogenesis (IMEC), Faculty of Sciences of Bizerte, University of Carthage, Zarzouna 7021, Tunisia.
Department of Immuno-Histo-Cytology, Salah Azaiz Cancer Institute, Tunis, Tunisia.
J Clin Med Res. 2022 Oct;14(10):416-424. doi: 10.14740/jocmr4785. Epub 2022 Oct 28.
Signal transducers and activators of transcription 5a and 6 (STAT5a and STAT6) play a critical role in tumorigenesis of mammary glands. Based on previous studies, the breast cancer is largely dependent on hormone receptors. Consequently, it is very interesting to decipher the relationship between the STAT5a and STAT6 expression and the molecular distribution of estrogen receptors (ERs) and progesterone receptors (PRs) in mammary tumors.
Our study analyzed the expression of STAT5a and STAT6, ERα, ERβ and PR in 40 breast tumor tissues using quantitative real-time polymerase chain reaction (qRT-PCR). Furthermore, the Ki-67 and HER2 status were detected using immunohistochemistry.
STAT5a and STAT6 were retained in the majority of the cases studied. Increasing of STAT5a and STAT6 is significantly associated with ERs and PR. The coexpression of both STAT5a and STAT6 with ERs and PR is associated with high tumor grades. Moreover, the coexpression of STAT5a and STAT6 with ERα and PR is associated with a high proliferation index. In addition, (STAT6 + ERβ+) and (STAT6 + PR+) breast cancer subgroups are associated with lymph node infiltration (P = 0.001 and P = 0.03, respectively).
Our study results provide an interaction between STAT5a and STAT6 with ERs and PR inducing cell proliferation. Coexpression of STAT5a and STAT6 with ERs and PR can predict sensibility to hormonal therapy.
信号转导子和转录激活子5a和6(STAT5a和STAT6)在乳腺肿瘤发生过程中起关键作用。基于以往研究,乳腺癌很大程度上依赖激素受体。因此,解读STAT5a和STAT6表达与乳腺肿瘤中雌激素受体(ERs)和孕激素受体(PRs)的分子分布之间的关系非常有趣。
我们的研究使用定量实时聚合酶链反应(qRT-PCR)分析了40例乳腺肿瘤组织中STAT5a和STAT6、ERα、ERβ和PR的表达。此外,使用免疫组织化学检测Ki-67和HER2状态。
在大多数研究病例中检测到STAT5a和STAT6。STAT5a和STAT6的增加与ERs和PR显著相关。STAT5a和STAT6与ERs和PR的共表达与高肿瘤分级相关。此外,STAT5a和STAT6与ERα和PR的共表达与高增殖指数相关。另外,(STAT6 + ERβ+)和(STAT6 + PR+)乳腺癌亚组与淋巴结浸润相关(分别为P = 0.001和P = 0.03)。
我们的研究结果表明STAT5a和STAT6与ERs和PR之间存在相互作用,诱导细胞增殖。STAT5a和STAT6与ERs和PR的共表达可预测对激素治疗的敏感性。