ARID1 and BRG1 Expression in Endometrial Cancer

被引:0
作者
Kontomanolis, Emmanuel N. [1 ,5 ]
Symeonidis, Panagiotis [1 ,6 ]
Nikolettos, Konstantinos [1 ]
Perros, Paraskevas [2 ]
Rody, Achim [3 ]
Tsikouras, Panagiotis [1 ]
Nikolettos, Nikolaos [1 ]
Giatromanolaki, Alexandra [4 ]
机构
[1] Democritus Univ Thrace, Dept Obstet & Gynecol, Alexandroupolis, Greece
[2] Natl & Kapodistrian Univ Athens, Gen Hosp Athens ALEXANDRA, Dept Obstet & Gynecol 1, Athens, Greece
[3] Univ Hosp Schleswig Holstein, Dept Obstet & Gynecol, Lubeck, Germany
[4] Democritus Univ Thrace, Dept Pathol, Alexandroupolis, Greece
[5] Univ Hosp Alexandroupolis, Democritus Univ Thrace, Med Sch, Dept Obstet Gynecol,Obstet & Gynecol, Alexandroupolis, Greece
[6] Natl & Kapodistrian Univ Athens, Gen Hosp Athens ALEXANDRA, Dept Obstet & Gynecol 1, Obstet & Gynecol, Lourou & Vasilissis Sofias Ave, Athens 11528, Greece
来源
IN VIVO | 2024年 / 38卷 / 03期
关键词
USEFUL MARKER; TUMOR; PROGNOSIS; GENES;
D O I
10.21873/invivo.13563
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: Endometrial cancer (EC) is the predominant malignancy among gynecologic cancers and ranks fourth among all types of cancer. Recently, researchers have focused on the development of new prognostic biomarkers. Subunits of the SWI/SNF protein complex, like the ARID1 and BRG1, have been associated with the development of endometrial cancer. The present study aimed to evaluate the expression patterns of ARID1A and BRG1 in a collection of endometrioid adenocarcinomas of the uterus using immunohistochemistry. Patients and Methods: The study comprised a total of thirty-three individuals diagnosed with stage I endometrioid endometrial cancer, treated with radical hysterectomy. The histological material was then examined to assess the cytoplasmic and nuclear expression of the proteins. Results: ARID1A exhibited expression in both the cytoplasm and nucleus of cancer cells, whereas BRG1 was mainly expressed in the nuclei. In addition, ARID1A exhibited a notable decrease in expression in grade 3 histology, with no significant correlation with the depth of myometrial invasion. The reduced expression was highly related to tumor expansion into the endocervix. The findings demonstrated a total absence of ARID1A expression in 27% of endometrioid carcinomas, with a significant reduction in expression in an additional 51% of cancer cells. These findings align with the most recent published data. In contrast, in the current study, BRG1 was rarely down -regulated and was extensively expressed in the majority of endometrioid carcinomas, preventing the possibility of statistical analysis. Conclusion: In summary, ARID1A expression loss can be used as a biomarker to guide post -operative therapy; however, further investigation is needed, especially for early -stage endometrial cancer.
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收藏
页码:1260 / 1265
页数:6
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