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New Steroidal Selenides as Proapoptotic Factors

Cytostatic and pro-apoptotic effects of selenium steroid derivatives against HeLa cells were determined. The highest cytostatic activity was shown by derivative 4 (GI(50) 25.0 µM, almost complete growth inhibition after three days of culture, and over 97% of apoptotic and dead cells at 200 µM). The...

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Autores principales: Jastrzebska, Izabella, Wawrusiewicz-Kurylonek, Natalia, Grześ, Paweł A., Ratkiewicz, Artur, Grabowska, Ewa, Czerniecka, Magdalena, Czyżewska, Urszula, Tylicki, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673341/
https://www.ncbi.nlm.nih.gov/pubmed/38005248
http://dx.doi.org/10.3390/molecules28227528
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author Jastrzebska, Izabella
Wawrusiewicz-Kurylonek, Natalia
Grześ, Paweł A.
Ratkiewicz, Artur
Grabowska, Ewa
Czerniecka, Magdalena
Czyżewska, Urszula
Tylicki, Adam
author_facet Jastrzebska, Izabella
Wawrusiewicz-Kurylonek, Natalia
Grześ, Paweł A.
Ratkiewicz, Artur
Grabowska, Ewa
Czerniecka, Magdalena
Czyżewska, Urszula
Tylicki, Adam
author_sort Jastrzebska, Izabella
collection PubMed
description Cytostatic and pro-apoptotic effects of selenium steroid derivatives against HeLa cells were determined. The highest cytostatic activity was shown by derivative 4 (GI(50) 25.0 µM, almost complete growth inhibition after three days of culture, and over 97% of apoptotic and dead cells at 200 µM). The results of our study (cell number measurements, apoptosis profile, relative expression of apoptosis-related APAF1, BID, and mevalonate pathway-involved HMGCR, SQLE, CYP51A1, and PDHB genes, and computational chemistry data) support the hypothesis that tested selenosteroids induce the extrinsic pathway of apoptosis by affecting the cell membrane as cholesterol antimetabolites. An additional mechanism of action is possible through a direct action of derivative 4 to inhibit PDHB expression in a way similar to steroid hormones.
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spelling pubmed-106733412023-11-10 New Steroidal Selenides as Proapoptotic Factors Jastrzebska, Izabella Wawrusiewicz-Kurylonek, Natalia Grześ, Paweł A. Ratkiewicz, Artur Grabowska, Ewa Czerniecka, Magdalena Czyżewska, Urszula Tylicki, Adam Molecules Article Cytostatic and pro-apoptotic effects of selenium steroid derivatives against HeLa cells were determined. The highest cytostatic activity was shown by derivative 4 (GI(50) 25.0 µM, almost complete growth inhibition after three days of culture, and over 97% of apoptotic and dead cells at 200 µM). The results of our study (cell number measurements, apoptosis profile, relative expression of apoptosis-related APAF1, BID, and mevalonate pathway-involved HMGCR, SQLE, CYP51A1, and PDHB genes, and computational chemistry data) support the hypothesis that tested selenosteroids induce the extrinsic pathway of apoptosis by affecting the cell membrane as cholesterol antimetabolites. An additional mechanism of action is possible through a direct action of derivative 4 to inhibit PDHB expression in a way similar to steroid hormones. MDPI 2023-11-10 /pmc/articles/PMC10673341/ /pubmed/38005248 http://dx.doi.org/10.3390/molecules28227528 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jastrzebska, Izabella
Wawrusiewicz-Kurylonek, Natalia
Grześ, Paweł A.
Ratkiewicz, Artur
Grabowska, Ewa
Czerniecka, Magdalena
Czyżewska, Urszula
Tylicki, Adam
New Steroidal Selenides as Proapoptotic Factors
title New Steroidal Selenides as Proapoptotic Factors
title_full New Steroidal Selenides as Proapoptotic Factors
title_fullStr New Steroidal Selenides as Proapoptotic Factors
title_full_unstemmed New Steroidal Selenides as Proapoptotic Factors
title_short New Steroidal Selenides as Proapoptotic Factors
title_sort new steroidal selenides as proapoptotic factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673341/
https://www.ncbi.nlm.nih.gov/pubmed/38005248
http://dx.doi.org/10.3390/molecules28227528
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