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Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma

BACKGROUND: To explore the expression and correlation of B-cell-specific Moloney murine leukemia virus insertion site 1 (Bmi-1), astrocyte elevated gene-1 (AEG-1) and fragile histidine triad (FHIT) in bladder transitional cell carcinoma (BTCC). METHODS: Forty-six tissue samples were obtained from pa...

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Autores principales: Su, Wei, Li, Chengwen, Li, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797676/
https://www.ncbi.nlm.nih.gov/pubmed/35117481
http://dx.doi.org/10.21037/tcr.2020.01.13
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author Su, Wei
Li, Chengwen
Li, Xin
author_facet Su, Wei
Li, Chengwen
Li, Xin
author_sort Su, Wei
collection PubMed
description BACKGROUND: To explore the expression and correlation of B-cell-specific Moloney murine leukemia virus insertion site 1 (Bmi-1), astrocyte elevated gene-1 (AEG-1) and fragile histidine triad (FHIT) in bladder transitional cell carcinoma (BTCC). METHODS: Forty-six tissue samples were obtained from patients diagnosed with primary bladder cancer during the first radical cystectomy between June 2010 and January 2014. The expression of Bmi-1, AEG-1 and FHIT in normal tissues and BTCC tissues in different histological cell types, clinical pathological stages and lymph node metastatic status were evaluated by quantitative real time polymerase chain reaction (qRT-PCR), Western blot and immunohistochemistry. Relationships between Bmi-1, AEG-1 and FHIT were determined using linear correlation coefficient. RESULTS: The results of qRT-PCR showed the relative expression of Bmi-1 and AEG-1 were higher and the expression of FHIT was lower in BTCC tissues than those in normal tissues, whether in different histological cell types, clinical pathological stages or lymph node metastatic status (P<0.05). Similarly, the up-regulated expression of Bmi-1 and AEG-1 and down-regulated expression of FHIT in BTCC tissues were observed by the Western blot and immunohistochemistry compared with normal tissues (P<0.05). Linear correlation analysis showed the expression of Bmi-1 was positively correlated with AEG-1 (r>0.90, P<0.01), which was negatively correlated with the expression of FHIT, respectively (r=−0.84, P<0.05). CONCLUSIONS: The study demonstrated the up-regulated expression of Bmi-1 and AEG-1 and the down-regulated expression of FHIT in BTCC tissues. The interaction of Bmi-1, AEG-1 and FHIT may involve in the tumorigenesis, progression and invasion of BTCC through NF-κB/MMP-9 pathway.
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spelling pubmed-87976762022-02-02 Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma Su, Wei Li, Chengwen Li, Xin Transl Cancer Res Original Article BACKGROUND: To explore the expression and correlation of B-cell-specific Moloney murine leukemia virus insertion site 1 (Bmi-1), astrocyte elevated gene-1 (AEG-1) and fragile histidine triad (FHIT) in bladder transitional cell carcinoma (BTCC). METHODS: Forty-six tissue samples were obtained from patients diagnosed with primary bladder cancer during the first radical cystectomy between June 2010 and January 2014. The expression of Bmi-1, AEG-1 and FHIT in normal tissues and BTCC tissues in different histological cell types, clinical pathological stages and lymph node metastatic status were evaluated by quantitative real time polymerase chain reaction (qRT-PCR), Western blot and immunohistochemistry. Relationships between Bmi-1, AEG-1 and FHIT were determined using linear correlation coefficient. RESULTS: The results of qRT-PCR showed the relative expression of Bmi-1 and AEG-1 were higher and the expression of FHIT was lower in BTCC tissues than those in normal tissues, whether in different histological cell types, clinical pathological stages or lymph node metastatic status (P<0.05). Similarly, the up-regulated expression of Bmi-1 and AEG-1 and down-regulated expression of FHIT in BTCC tissues were observed by the Western blot and immunohistochemistry compared with normal tissues (P<0.05). Linear correlation analysis showed the expression of Bmi-1 was positively correlated with AEG-1 (r>0.90, P<0.01), which was negatively correlated with the expression of FHIT, respectively (r=−0.84, P<0.05). CONCLUSIONS: The study demonstrated the up-regulated expression of Bmi-1 and AEG-1 and the down-regulated expression of FHIT in BTCC tissues. The interaction of Bmi-1, AEG-1 and FHIT may involve in the tumorigenesis, progression and invasion of BTCC through NF-κB/MMP-9 pathway. AME Publishing Company 2020-03 /pmc/articles/PMC8797676/ /pubmed/35117481 http://dx.doi.org/10.21037/tcr.2020.01.13 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Su, Wei
Li, Chengwen
Li, Xin
Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma
title Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma
title_full Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma
title_fullStr Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma
title_full_unstemmed Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma
title_short Expression and correlation of Bmi-1, AEG-1 and FHIT in bladder transitional cell carcinoma
title_sort expression and correlation of bmi-1, aeg-1 and fhit in bladder transitional cell carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797676/
https://www.ncbi.nlm.nih.gov/pubmed/35117481
http://dx.doi.org/10.21037/tcr.2020.01.13
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