Cargando…
EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer
BACKGROUND: The epithelial to mesenchymal transition (EMT) is a molecular process through which an epithelial cell undergoes transdifferentiation into a mesenchymal phenotype. The role of EMT in embryogenesis is well-characterized and increasing evidence suggests that elements of the transition may...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342883/ https://www.ncbi.nlm.nih.gov/pubmed/22429801 http://dx.doi.org/10.1186/1471-2407-12-91 |
_version_ | 1782231742622466048 |
---|---|
author | Haslehurst, Alexandria M Koti, Madhuri Dharsee, Moyez Nuin, Paulo Evans, Ken Geraci, Joseph Childs, Timothy Chen, Jian Li, Jieran Weberpals, Johanne Davey, Scott Squire, Jeremy Park, Paul C Feilotter, Harriet |
author_facet | Haslehurst, Alexandria M Koti, Madhuri Dharsee, Moyez Nuin, Paulo Evans, Ken Geraci, Joseph Childs, Timothy Chen, Jian Li, Jieran Weberpals, Johanne Davey, Scott Squire, Jeremy Park, Paul C Feilotter, Harriet |
author_sort | Haslehurst, Alexandria M |
collection | PubMed |
description | BACKGROUND: The epithelial to mesenchymal transition (EMT) is a molecular process through which an epithelial cell undergoes transdifferentiation into a mesenchymal phenotype. The role of EMT in embryogenesis is well-characterized and increasing evidence suggests that elements of the transition may be important in other processes, including metastasis and drug resistance in various different cancers. METHODS: Agilent 4 × 44 K whole human genome arrays and selected reaction monitoring mass spectrometry were used to investigate mRNA and protein expression in A2780 cisplatin sensitive and resistant cell lines. Invasion and migration were assessed using Boyden chamber assays. Gene knockdown of snail and slug was done using targeted siRNA. Clinical relevance of the EMT pathway was assessed in a cohort of primary ovarian tumours using data from Affymetrix GeneChip Human Genome U133 plus 2.0 arrays. RESULTS: Morphological and phenotypic hallmarks of EMT were identified in the chemoresistant cells. Subsequent gene expression profiling revealed upregulation of EMT-related transcription factors including snail, slug, twist2 and zeb2. Proteomic analysis demonstrated up regulation of Snail and Slug as well as the mesenchymal marker Vimentin, and down regulation of E-cadherin, an epithelial marker. By reducing expression of snail and slug, the mesenchymal phenotype was largely reversed and cells were resensitized to cisplatin. Finally, gene expression data from primary tumours mirrored the finding that an EMT-like pathway is activated in resistant tumours relative to sensitive tumours, suggesting that the involvement of this transition may not be limited to in vitro drug effects. CONCLUSIONS: This work strongly suggests that genes associated with EMT may play a significant role in cisplatin resistance in ovarian cancer, therefore potentially leading to the development of predictive biomarkers of drug response or novel therapeutic strategies for overcoming drug resistance. |
format | Online Article Text |
id | pubmed-3342883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33428832012-05-04 EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer Haslehurst, Alexandria M Koti, Madhuri Dharsee, Moyez Nuin, Paulo Evans, Ken Geraci, Joseph Childs, Timothy Chen, Jian Li, Jieran Weberpals, Johanne Davey, Scott Squire, Jeremy Park, Paul C Feilotter, Harriet BMC Cancer Research Article BACKGROUND: The epithelial to mesenchymal transition (EMT) is a molecular process through which an epithelial cell undergoes transdifferentiation into a mesenchymal phenotype. The role of EMT in embryogenesis is well-characterized and increasing evidence suggests that elements of the transition may be important in other processes, including metastasis and drug resistance in various different cancers. METHODS: Agilent 4 × 44 K whole human genome arrays and selected reaction monitoring mass spectrometry were used to investigate mRNA and protein expression in A2780 cisplatin sensitive and resistant cell lines. Invasion and migration were assessed using Boyden chamber assays. Gene knockdown of snail and slug was done using targeted siRNA. Clinical relevance of the EMT pathway was assessed in a cohort of primary ovarian tumours using data from Affymetrix GeneChip Human Genome U133 plus 2.0 arrays. RESULTS: Morphological and phenotypic hallmarks of EMT were identified in the chemoresistant cells. Subsequent gene expression profiling revealed upregulation of EMT-related transcription factors including snail, slug, twist2 and zeb2. Proteomic analysis demonstrated up regulation of Snail and Slug as well as the mesenchymal marker Vimentin, and down regulation of E-cadherin, an epithelial marker. By reducing expression of snail and slug, the mesenchymal phenotype was largely reversed and cells were resensitized to cisplatin. Finally, gene expression data from primary tumours mirrored the finding that an EMT-like pathway is activated in resistant tumours relative to sensitive tumours, suggesting that the involvement of this transition may not be limited to in vitro drug effects. CONCLUSIONS: This work strongly suggests that genes associated with EMT may play a significant role in cisplatin resistance in ovarian cancer, therefore potentially leading to the development of predictive biomarkers of drug response or novel therapeutic strategies for overcoming drug resistance. BioMed Central 2012-03-19 /pmc/articles/PMC3342883/ /pubmed/22429801 http://dx.doi.org/10.1186/1471-2407-12-91 Text en Copyright ©2012 Haslehurst et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Haslehurst, Alexandria M Koti, Madhuri Dharsee, Moyez Nuin, Paulo Evans, Ken Geraci, Joseph Childs, Timothy Chen, Jian Li, Jieran Weberpals, Johanne Davey, Scott Squire, Jeremy Park, Paul C Feilotter, Harriet EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
title | EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
title_full | EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
title_fullStr | EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
title_full_unstemmed | EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
title_short | EMT transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
title_sort | emt transcription factors snail and slug directly contribute to cisplatin resistance in ovarian cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342883/ https://www.ncbi.nlm.nih.gov/pubmed/22429801 http://dx.doi.org/10.1186/1471-2407-12-91 |
work_keys_str_mv | AT haslehurstalexandriam emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT kotimadhuri emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT dharseemoyez emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT nuinpaulo emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT evansken emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT geracijoseph emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT childstimothy emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT chenjian emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT lijieran emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT weberpalsjohanne emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT daveyscott emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT squirejeremy emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT parkpaulc emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer AT feilotterharriet emttranscriptionfactorssnailandslugdirectlycontributetocisplatinresistanceinovariancancer |