Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells

Previous research indicates that carcinogenesis involves disrupting the functions of numerous genes, including factors involved in the regulation of transcription and cell proliferation. For these reasons, in endometrial carcinogenesis, we decided to investigate the expression of TSG101 (a suppresso...

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Main Authors: Rafał Ziemiński, Aleksandra Stupak, Maciej Kwiatek, Tomasz Gęca, Alicja Warowicka, Karolina Hejne, Anna Kwaśniewska, Anna Goździcka-Józefiak, Wojciech Kwaśniewski
Format: Article
Language:English
Published: MDPI AG 2024-03-01
Series:Cells
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Online Access:https://www.mdpi.com/2073-4409/13/7/580
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author Rafał Ziemiński
Aleksandra Stupak
Maciej Kwiatek
Tomasz Gęca
Alicja Warowicka
Karolina Hejne
Anna Kwaśniewska
Anna Goździcka-Józefiak
Wojciech Kwaśniewski
author_facet Rafał Ziemiński
Aleksandra Stupak
Maciej Kwiatek
Tomasz Gęca
Alicja Warowicka
Karolina Hejne
Anna Kwaśniewska
Anna Goździcka-Józefiak
Wojciech Kwaśniewski
author_sort Rafał Ziemiński
collection DOAJ
description Previous research indicates that carcinogenesis involves disrupting the functions of numerous genes, including factors involved in the regulation of transcription and cell proliferation. For these reasons, in endometrial carcinogenesis, we decided to investigate the expression of TSG101 (a suppressor of tumor transformation) and LSF (a transcription factor involved in numerous cellular processes, such as cell cycle regulation, cell growth, development, and apoptosis). LSF may be involved in the regulation of TSG101 expression. The research material consisted of endometrial cancer samples from 60 patients. The control group consisted of normal endometrium samples donated by 60 women undergoing surgery for benign diseases of the female reproductive organs. The samples were subjected to immunohistochemical staining with antibodies specific to TSG101 and LSF. Specific antibodies were used to identify TSG101 and LSF in the examined histopathological preparations. An approximately 14-fold lower risk of endometrial cancer development was observed in patients with TSG expression in more than 75% of the assessed cells (4% vs. 36%; OR = 0.07; <i>p</i> = 0.0182). There was a four-fold lower risk of endometrial cancer development in patients with LSF expression in more than 50% of the assessed cells (32% vs. 64%; OR = 0.26; <i>p</i> = 0.0262). A more than three-fold lower risk of endometrial cancer development was observed in patients with LSF expression in more than 75% of the assessed cells (24% vs. 52%; OR = 0.29; <i>p</i> = 0.0454). Endometrial cancer was diagnosed in those with a lower level of TSG101 expression than in those with a cancer-free endometrium. Decreased expression of TSG101 may be a marker of endometrial cancer, and increased expression of LSF when diagnosed with endometrial cancer may indicate greater advancement of the disease. These markers might be used as diagnostic and prognostic markers—however, there is a lack of a correlation between them.
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spelling doaj.art-e0d8732251aa42d1851f9f2f9aad455c2024-04-12T13:16:26ZengMDPI AGCells2073-44092024-03-0113758010.3390/cells13070580Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial CellsRafał Ziemiński0Aleksandra Stupak1Maciej Kwiatek2Tomasz Gęca3Alicja Warowicka4Karolina Hejne5Anna Kwaśniewska6Anna Goździcka-Józefiak7Wojciech Kwaśniewski8Department of Obstetrics and Pathology of Pregnancy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Obstetrics and Pathology of Pregnancy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Obstetrics and Pathology of Pregnancy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Obstetrics and Pathology of Pregnancy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Molecular Virology, Institute of Experimental Biology, Adam Mickiewicz University in Poznan, 61-712 Poznań, PolandDepartment of Pathomorphology and Forensic Medicine, School of Medicine, Collegium Medicum, University of Warmia and Mazury, 11-082 Olsztyn, PolandDepartment of Obstetrics and Pathology of Pregnancy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Molecular Virology, Institute of Experimental Biology, Adam Mickiewicz University in Poznan, 61-712 Poznań, PolandDepartment of Gynecology Oncology and Gynecology, Medical University of Lublin, 20-059 Lublin, PolandPrevious research indicates that carcinogenesis involves disrupting the functions of numerous genes, including factors involved in the regulation of transcription and cell proliferation. For these reasons, in endometrial carcinogenesis, we decided to investigate the expression of TSG101 (a suppressor of tumor transformation) and LSF (a transcription factor involved in numerous cellular processes, such as cell cycle regulation, cell growth, development, and apoptosis). LSF may be involved in the regulation of TSG101 expression. The research material consisted of endometrial cancer samples from 60 patients. The control group consisted of normal endometrium samples donated by 60 women undergoing surgery for benign diseases of the female reproductive organs. The samples were subjected to immunohistochemical staining with antibodies specific to TSG101 and LSF. Specific antibodies were used to identify TSG101 and LSF in the examined histopathological preparations. An approximately 14-fold lower risk of endometrial cancer development was observed in patients with TSG expression in more than 75% of the assessed cells (4% vs. 36%; OR = 0.07; <i>p</i> = 0.0182). There was a four-fold lower risk of endometrial cancer development in patients with LSF expression in more than 50% of the assessed cells (32% vs. 64%; OR = 0.26; <i>p</i> = 0.0262). A more than three-fold lower risk of endometrial cancer development was observed in patients with LSF expression in more than 75% of the assessed cells (24% vs. 52%; OR = 0.29; <i>p</i> = 0.0454). Endometrial cancer was diagnosed in those with a lower level of TSG101 expression than in those with a cancer-free endometrium. Decreased expression of TSG101 may be a marker of endometrial cancer, and increased expression of LSF when diagnosed with endometrial cancer may indicate greater advancement of the disease. These markers might be used as diagnostic and prognostic markers—however, there is a lack of a correlation between them.https://www.mdpi.com/2073-4409/13/7/580carcinogenesisLSF transcription factorTSG101endometrial cancer
spellingShingle Rafał Ziemiński
Aleksandra Stupak
Maciej Kwiatek
Tomasz Gęca
Alicja Warowicka
Karolina Hejne
Anna Kwaśniewska
Anna Goździcka-Józefiak
Wojciech Kwaśniewski
Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells
Cells
carcinogenesis
LSF transcription factor
TSG101
endometrial cancer
title Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells
title_full Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells
title_fullStr Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells
title_full_unstemmed Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells
title_short Analysis of the Expression of LSF Transcription Factor in the Regulation of Transcription and TSG101 during the Neoplastic Transformation of Endometrial Cells
title_sort analysis of the expression of lsf transcription factor in the regulation of transcription and tsg101 during the neoplastic transformation of endometrial cells
topic carcinogenesis
LSF transcription factor
TSG101
endometrial cancer
url https://www.mdpi.com/2073-4409/13/7/580
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