Cargando…
Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells
Despite progress achieved in cancer chemotherapy in recent decades, adverse effects remain a limiting factor for a number of patients with colorectal cancer, suggesting the requirement for novel therapeutic strategies. Gene therapy appears to be a promising strategy for treating cancer. The present...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704315/ https://www.ncbi.nlm.nih.gov/pubmed/29201172 http://dx.doi.org/10.3892/etm.2017.5154 |
_version_ | 1783281867279040512 |
---|---|
author | Ye, Ling Yang, Yuan Ma, Xin-Yu Li, Dan Xu, Mei-Li Tan, Pan Long, Li-Min Wang, Hai-Qin Liu, Ting Guo, Yong-Hong |
author_facet | Ye, Ling Yang, Yuan Ma, Xin-Yu Li, Dan Xu, Mei-Li Tan, Pan Long, Li-Min Wang, Hai-Qin Liu, Ting Guo, Yong-Hong |
author_sort | Ye, Ling |
collection | PubMed |
description | Despite progress achieved in cancer chemotherapy in recent decades, adverse effects remain a limiting factor for a number of patients with colorectal cancer, suggesting the requirement for novel therapeutic strategies. Gene therapy appears to be a promising strategy for treating cancer. The present study aimed to investigate the anti-tumor effect of a combined gene therapy, using Survivin downregulation by RNAi and a fusion suicide gene yCDglyTK therapy system. A triple-gene vector expressing Survivin-targeted small hairpin RNA (Survivin-shRNA) and fusion suicide gene yCDglyTK was constructed, and administered to HCT116 cells. Survivin expression decreased significantly and yCDglyTK fusion gene expression was confirmed by both reverse transcription-quantitative polymerase chain reaction and western blot analysis. Introduction of Survivin-shRNA into yCDglyTK/prodrug system eradicated colon cancer cells and induced apoptosis more effectively. Furthermore, this therapeutic system is able to inhibit the migration of HCT116 cells. These results indicate that the recombinant plasmid may serve as a novel gene therapy approach to treat colorectal carcinoma. |
format | Online Article Text |
id | pubmed-5704315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-57043152017-11-30 Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells Ye, Ling Yang, Yuan Ma, Xin-Yu Li, Dan Xu, Mei-Li Tan, Pan Long, Li-Min Wang, Hai-Qin Liu, Ting Guo, Yong-Hong Exp Ther Med Articles Despite progress achieved in cancer chemotherapy in recent decades, adverse effects remain a limiting factor for a number of patients with colorectal cancer, suggesting the requirement for novel therapeutic strategies. Gene therapy appears to be a promising strategy for treating cancer. The present study aimed to investigate the anti-tumor effect of a combined gene therapy, using Survivin downregulation by RNAi and a fusion suicide gene yCDglyTK therapy system. A triple-gene vector expressing Survivin-targeted small hairpin RNA (Survivin-shRNA) and fusion suicide gene yCDglyTK was constructed, and administered to HCT116 cells. Survivin expression decreased significantly and yCDglyTK fusion gene expression was confirmed by both reverse transcription-quantitative polymerase chain reaction and western blot analysis. Introduction of Survivin-shRNA into yCDglyTK/prodrug system eradicated colon cancer cells and induced apoptosis more effectively. Furthermore, this therapeutic system is able to inhibit the migration of HCT116 cells. These results indicate that the recombinant plasmid may serve as a novel gene therapy approach to treat colorectal carcinoma. D.A. Spandidos 2017-11 2017-09-20 /pmc/articles/PMC5704315/ /pubmed/29201172 http://dx.doi.org/10.3892/etm.2017.5154 Text en Copyright: © Ye et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Ye, Ling Yang, Yuan Ma, Xin-Yu Li, Dan Xu, Mei-Li Tan, Pan Long, Li-Min Wang, Hai-Qin Liu, Ting Guo, Yong-Hong Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells |
title | Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells |
title_full | Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells |
title_fullStr | Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells |
title_full_unstemmed | Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells |
title_short | Construction of a novel vector expressing Survivin-shRNA and fusion suicide gene yCDglyTK and its application in inhibiting proliferation and migration of colon cancer cells |
title_sort | construction of a novel vector expressing survivin-shrna and fusion suicide gene ycdglytk and its application in inhibiting proliferation and migration of colon cancer cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704315/ https://www.ncbi.nlm.nih.gov/pubmed/29201172 http://dx.doi.org/10.3892/etm.2017.5154 |
work_keys_str_mv | AT yeling constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT yangyuan constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT maxinyu constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT lidan constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT xumeili constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT tanpan constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT longlimin constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT wanghaiqin constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT liuting constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells AT guoyonghong constructionofanovelvectorexpressingsurvivinshrnaandfusionsuicidegeneycdglytkanditsapplicationininhibitingproliferationandmigrationofcoloncancercells |