Cargando…
Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents
A new series of acrylic acid and acrylate ester derivatives as modified analogs of tubulin polymerization inhibitors were designed and synthesized. The antiproliferative activity of the constructed molecules was investigated against MCF-7 breast carcinoma cells using CA-4 as positive molecule. Methy...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402871/ https://www.ncbi.nlm.nih.gov/pubmed/37546218 http://dx.doi.org/10.1039/d3ra03849a |
_version_ | 1785084937025617920 |
---|---|
author | Alshaya, Dalal Sulaiman Tawakul, Rana M. O. Zaki, Islam Abu Almaaty, Ali H. Fayad, Eman Abd El-Aziz, Yasmin M. |
author_facet | Alshaya, Dalal Sulaiman Tawakul, Rana M. O. Zaki, Islam Abu Almaaty, Ali H. Fayad, Eman Abd El-Aziz, Yasmin M. |
author_sort | Alshaya, Dalal Sulaiman |
collection | PubMed |
description | A new series of acrylic acid and acrylate ester derivatives as modified analogs of tubulin polymerization inhibitors were designed and synthesized. The antiproliferative activity of the constructed molecules was investigated against MCF-7 breast carcinoma cells using CA-4 as positive molecule. Methyl acrylate ester 6e emerged as the most potent cytotoxic agent against MCF-7 cells, with an IC(50) value of 2.57 ± 0.16 μM. Also, methyl acrylate ester molecule 6e showed good β-tubulin polymerization inhibition activity. Cellular cycle analysis showed that compound 6e can arrest MCF-7 cells at the G2/M phase. In addition, this compound produced a significant increase in apoptotic power as compared to control untreated MCF-7 cells. Furthermore, the effect of acrylate ester 6e on the gene expression levels of p53, Bax and Bcl-2 was investigated. This molecule increased the expression levels of both p53 and Bax, and decreased the gene expression level of Bcl-2 as compared to control untreated MCF-7 carcinoma cells. |
format | Online Article Text |
id | pubmed-10402871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-104028712023-08-05 Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents Alshaya, Dalal Sulaiman Tawakul, Rana M. O. Zaki, Islam Abu Almaaty, Ali H. Fayad, Eman Abd El-Aziz, Yasmin M. RSC Adv Chemistry A new series of acrylic acid and acrylate ester derivatives as modified analogs of tubulin polymerization inhibitors were designed and synthesized. The antiproliferative activity of the constructed molecules was investigated against MCF-7 breast carcinoma cells using CA-4 as positive molecule. Methyl acrylate ester 6e emerged as the most potent cytotoxic agent against MCF-7 cells, with an IC(50) value of 2.57 ± 0.16 μM. Also, methyl acrylate ester molecule 6e showed good β-tubulin polymerization inhibition activity. Cellular cycle analysis showed that compound 6e can arrest MCF-7 cells at the G2/M phase. In addition, this compound produced a significant increase in apoptotic power as compared to control untreated MCF-7 cells. Furthermore, the effect of acrylate ester 6e on the gene expression levels of p53, Bax and Bcl-2 was investigated. This molecule increased the expression levels of both p53 and Bax, and decreased the gene expression level of Bcl-2 as compared to control untreated MCF-7 carcinoma cells. The Royal Society of Chemistry 2023-08-04 /pmc/articles/PMC10402871/ /pubmed/37546218 http://dx.doi.org/10.1039/d3ra03849a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Alshaya, Dalal Sulaiman Tawakul, Rana M. O. Zaki, Islam Abu Almaaty, Ali H. Fayad, Eman Abd El-Aziz, Yasmin M. Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
title | Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
title_full | Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
title_fullStr | Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
title_full_unstemmed | Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
title_short | Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
title_sort | design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402871/ https://www.ncbi.nlm.nih.gov/pubmed/37546218 http://dx.doi.org/10.1039/d3ra03849a |
work_keys_str_mv | AT alshayadalalsulaiman designsynthesisandantiproliferativescreeningofnewlysynthesizedacrylatederivativesaspotentialanticanceragents AT tawakulranamo designsynthesisandantiproliferativescreeningofnewlysynthesizedacrylatederivativesaspotentialanticanceragents AT zakiislam designsynthesisandantiproliferativescreeningofnewlysynthesizedacrylatederivativesaspotentialanticanceragents AT abualmaatyalih designsynthesisandantiproliferativescreeningofnewlysynthesizedacrylatederivativesaspotentialanticanceragents AT fayademan designsynthesisandantiproliferativescreeningofnewlysynthesizedacrylatederivativesaspotentialanticanceragents AT abdelazizyasminm designsynthesisandantiproliferativescreeningofnewlysynthesizedacrylatederivativesaspotentialanticanceragents |