Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged Retardation of Neuroblastoma Cell Division
Deregulation of the expression of the genes that are involved in the control of the cell cycle impairs cellular differentiation and leads to cell death. This process can result in uncontrollable cell proliferation and, subsequently, cancer development. In this study, we examined the effect of the si...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
A.I. Gordeyev
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347608/ https://www.ncbi.nlm.nih.gov/pubmed/22649691 |
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author | Akimov, I.A. Chernolovskaya, E.L. Spitsyna, Yu.E. Ryabchikova, E.I. Zenkova, M.A. |
author_facet | Akimov, I.A. Chernolovskaya, E.L. Spitsyna, Yu.E. Ryabchikova, E.I. Zenkova, M.A. |
author_sort | Akimov, I.A. |
collection | PubMed |
description | Deregulation of the expression of the genes that are involved in the control of the cell cycle impairs cellular differentiation and leads to cell death. This process can result in uncontrollable cell proliferation and, subsequently, cancer development. In this study, we examined the effect of the silencing of cancer-related genes by small interfering RNAs (siRNA) targeted at mRNAof Her2, cyclin B1 (CCNB1), and protein kinase C(PKC) on the proliferation of human cancer cells of different origins. Maximum silencing ofCCNB1,Her2(in KB-3-1, SK-N-MC, MCF-7 cells), andPKC(in MCF-7 cells) was achieved 72 h after transfection of the corresponding siRNAs, and 12 days after the transfection, the initial levels of the target mRNAs were fully recovered. Silencing ofHer2,CCNB1,andPKCdifferently effected the proliferation of the cell lines under study. The most pronounced antiproliferative action of the investigated siRNAs was observed in neuroblastoma SK-N-MC cells (3 – 10-fold reduction in the proliferation rate) even after the recovery of the initial levels of expression ofthe Her2,CCNB1, andPKС genes. The obtained data indicate that theCCNB1 andPKCgenes can be used as targets in the development of drugs for neuroblastoma treatment. |
format | Online Article Text |
id | pubmed-3347608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | A.I. Gordeyev |
record_format | MEDLINE/PubMed |
spelling | pubmed-33476082012-05-30 Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged Retardation of Neuroblastoma Cell Division Akimov, I.A. Chernolovskaya, E.L. Spitsyna, Yu.E. Ryabchikova, E.I. Zenkova, M.A. Acta Naturae Research Article Deregulation of the expression of the genes that are involved in the control of the cell cycle impairs cellular differentiation and leads to cell death. This process can result in uncontrollable cell proliferation and, subsequently, cancer development. In this study, we examined the effect of the silencing of cancer-related genes by small interfering RNAs (siRNA) targeted at mRNAof Her2, cyclin B1 (CCNB1), and protein kinase C(PKC) on the proliferation of human cancer cells of different origins. Maximum silencing ofCCNB1,Her2(in KB-3-1, SK-N-MC, MCF-7 cells), andPKC(in MCF-7 cells) was achieved 72 h after transfection of the corresponding siRNAs, and 12 days after the transfection, the initial levels of the target mRNAs were fully recovered. Silencing ofHer2,CCNB1,andPKCdifferently effected the proliferation of the cell lines under study. The most pronounced antiproliferative action of the investigated siRNAs was observed in neuroblastoma SK-N-MC cells (3 – 10-fold reduction in the proliferation rate) even after the recovery of the initial levels of expression ofthe Her2,CCNB1, andPKС genes. The obtained data indicate that theCCNB1 andPKCgenes can be used as targets in the development of drugs for neuroblastoma treatment. A.I. Gordeyev 2011 /pmc/articles/PMC3347608/ /pubmed/22649691 Text en Copyright © 2011 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Akimov, I.A. Chernolovskaya, E.L. Spitsyna, Yu.E. Ryabchikova, E.I. Zenkova, M.A. Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged Retardation of Neuroblastoma Cell Division |
title | Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged
Retardation of Neuroblastoma Cell Division |
title_full | Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged
Retardation of Neuroblastoma Cell Division |
title_fullStr | Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged
Retardation of Neuroblastoma Cell Division |
title_full_unstemmed | Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged
Retardation of Neuroblastoma Cell Division |
title_short | Silencing of Her2, CCNB1 and PKC Genes by siRNA Results in Prolonged
Retardation of Neuroblastoma Cell Division |
title_sort | silencing of her2, ccnb1 and pkc genes by sirna results in prolonged
retardation of neuroblastoma cell division |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347608/ https://www.ncbi.nlm.nih.gov/pubmed/22649691 |
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