Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells.
We propose the hypothesis that loss of estrogen receptor function which leads to endocrine resistance in breast cancer, also results in trans-differentiation from an epithelial to a mesenchymal phenotype that is responsible for increased aggressiveness and metastatic propensity. siRNA mediated silen...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2011-01-01
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| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC3119661?pdf=render |
| _version_ | 1819069270913449984 |
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| author | Sanaa Al Saleh Fahd Al Mulla Yunus A Luqmani |
| author_facet | Sanaa Al Saleh Fahd Al Mulla Yunus A Luqmani |
| author_sort | Sanaa Al Saleh |
| collection | DOAJ |
| description | We propose the hypothesis that loss of estrogen receptor function which leads to endocrine resistance in breast cancer, also results in trans-differentiation from an epithelial to a mesenchymal phenotype that is responsible for increased aggressiveness and metastatic propensity. siRNA mediated silencing of the estrogen receptor in MCF7 breast cancer cells resulted in estrogen/tamoxifen resistant cells (pII) with altered morphology, increased motility with rearrangement and switch from a keratin/actin to a vimentin based cytoskeleton, and ability to invade simulated components of the extracellular matrix. Phenotypic profiling using an Affymetrix Human Genome U133 plus 2.0 GeneChip indicated geometric fold changes ≥ 3 in approximately 2500 identifiable unique sequences, with about 1270 of these being up-regulated in pII cells. Changes were associated with genes whose products are involved in cell motility, loss of cellular adhesion and interaction with the extracellular matrix. Selective analysis of the data also showed a shift from luminal to basal cell markers and increased expression of a wide spectrum of genes normally associated with mesenchymal characteristics, with consequent loss of epithelial specific markers. Over-expression of several peptide growth factors and their receptors are indicative of an increased contribution to the higher proliferative rates of pII cells as well as aiding their potential for metastatic activity. Signalling molecules that have been identified as key transcriptional drivers of epithelial to mesenchymal transition were also found to be elevated in pII cells. These data support our hypothesis that induced loss of estrogen receptor in previously estrogen/antiestrogen sensitive cells is a trigger for the concomitant loss of endocrine dependence and onset of a series of possibly parallel events that changes the cell from an epithelial to a mesenchymal type. Inhibition of this transition through targeting of specific mediators may offer a useful supplementary strategy to circumvent the effects of loss of endocrine sensitivity. |
| first_indexed | 2024-12-21T16:47:23Z |
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| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-12-21T16:47:23Z |
| publishDate | 2011-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-bf2dc64b8e1b4b6da6ceb751107b2be12022-12-21T18:56:58ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0166e2061010.1371/journal.pone.0020610Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells.Sanaa Al SalehFahd Al MullaYunus A LuqmaniWe propose the hypothesis that loss of estrogen receptor function which leads to endocrine resistance in breast cancer, also results in trans-differentiation from an epithelial to a mesenchymal phenotype that is responsible for increased aggressiveness and metastatic propensity. siRNA mediated silencing of the estrogen receptor in MCF7 breast cancer cells resulted in estrogen/tamoxifen resistant cells (pII) with altered morphology, increased motility with rearrangement and switch from a keratin/actin to a vimentin based cytoskeleton, and ability to invade simulated components of the extracellular matrix. Phenotypic profiling using an Affymetrix Human Genome U133 plus 2.0 GeneChip indicated geometric fold changes ≥ 3 in approximately 2500 identifiable unique sequences, with about 1270 of these being up-regulated in pII cells. Changes were associated with genes whose products are involved in cell motility, loss of cellular adhesion and interaction with the extracellular matrix. Selective analysis of the data also showed a shift from luminal to basal cell markers and increased expression of a wide spectrum of genes normally associated with mesenchymal characteristics, with consequent loss of epithelial specific markers. Over-expression of several peptide growth factors and their receptors are indicative of an increased contribution to the higher proliferative rates of pII cells as well as aiding their potential for metastatic activity. Signalling molecules that have been identified as key transcriptional drivers of epithelial to mesenchymal transition were also found to be elevated in pII cells. These data support our hypothesis that induced loss of estrogen receptor in previously estrogen/antiestrogen sensitive cells is a trigger for the concomitant loss of endocrine dependence and onset of a series of possibly parallel events that changes the cell from an epithelial to a mesenchymal type. Inhibition of this transition through targeting of specific mediators may offer a useful supplementary strategy to circumvent the effects of loss of endocrine sensitivity.http://europepmc.org/articles/PMC3119661?pdf=render |
| spellingShingle | Sanaa Al Saleh Fahd Al Mulla Yunus A Luqmani Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells. PLoS ONE |
| title | Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells. |
| title_full | Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells. |
| title_fullStr | Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells. |
| title_full_unstemmed | Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells. |
| title_short | Estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells. |
| title_sort | estrogen receptor silencing induces epithelial to mesenchymal transition in human breast cancer cells |
| url | http://europepmc.org/articles/PMC3119661?pdf=render |
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