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AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells

OBJECTIVE: SRSF1 is a splicing factor often times described as an oncoprotein. In the present work, we examined the expression of SRSF1 in human bladder carcinoma cells and detected the change of SRSF1 expression in BIU-87 cells after the treatment of chemotherapeutic drug. METHODS: Human bladder ca...

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Detalles Bibliográficos
Autores principales: Wang, Ping, Yu, Liu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842682/
http://dx.doi.org/10.21037/tau.2016.s068
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author Wang, Ping
Yu, Liu
author_facet Wang, Ping
Yu, Liu
author_sort Wang, Ping
collection PubMed
description OBJECTIVE: SRSF1 is a splicing factor often times described as an oncoprotein. In the present work, we examined the expression of SRSF1 in human bladder carcinoma cells and detected the change of SRSF1 expression in BIU-87 cells after the treatment of chemotherapeutic drug. METHODS: Human bladder carcinoma cells (BIU-87) were treated by growth factors with or without chemotherapeutic drug (pirarubicin) agents’ interference. The confirmed of SRSF1 expression in BIU-87 cells and the assessment of the chemotherapeutic drug’s function to SRSF1 protein was analyzed by Western blot. RESULTS: SRSF1 precisely expressed in human bladder carcinoma cells—BIU-87 cell line. Protein levels of SRSF1 significantly decreased after pirarubicin treatment in a higher concentration (1.6, 3.2 ug/mL) while slightly increased after the treatment in a lower concentration (0.4, 0.8 ug/mL). SRSF1 expression appeared as a peak form. CONCLUSIONS: This study tells the expression of SRSF1 BIU-87 cells and its variation after chemotherapeutic drug (pirarubicin) treatment. In conclusion, SRSF1 may act as a useful potential target for bladder carcinoma therapies.
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spelling pubmed-48426822016-05-09 AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells Wang, Ping Yu, Liu Transl Androl Urol Poster Presentation OBJECTIVE: SRSF1 is a splicing factor often times described as an oncoprotein. In the present work, we examined the expression of SRSF1 in human bladder carcinoma cells and detected the change of SRSF1 expression in BIU-87 cells after the treatment of chemotherapeutic drug. METHODS: Human bladder carcinoma cells (BIU-87) were treated by growth factors with or without chemotherapeutic drug (pirarubicin) agents’ interference. The confirmed of SRSF1 expression in BIU-87 cells and the assessment of the chemotherapeutic drug’s function to SRSF1 protein was analyzed by Western blot. RESULTS: SRSF1 precisely expressed in human bladder carcinoma cells—BIU-87 cell line. Protein levels of SRSF1 significantly decreased after pirarubicin treatment in a higher concentration (1.6, 3.2 ug/mL) while slightly increased after the treatment in a lower concentration (0.4, 0.8 ug/mL). SRSF1 expression appeared as a peak form. CONCLUSIONS: This study tells the expression of SRSF1 BIU-87 cells and its variation after chemotherapeutic drug (pirarubicin) treatment. In conclusion, SRSF1 may act as a useful potential target for bladder carcinoma therapies. AME Publishing Company 2016-04 /pmc/articles/PMC4842682/ http://dx.doi.org/10.21037/tau.2016.s068 Text en 2016 Translational Andrology and Urology. All rights reserved.
spellingShingle Poster Presentation
Wang, Ping
Yu, Liu
AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells
title AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells
title_full AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells
title_fullStr AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells
title_full_unstemmed AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells
title_short AB068. The splicing factor SRSF1 expression in human bladder carcinoma cells
title_sort ab068. the splicing factor srsf1 expression in human bladder carcinoma cells
topic Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842682/
http://dx.doi.org/10.21037/tau.2016.s068
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