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We are analyzing https://link.springer.com/article/10.1186/bcr1656.

Title:
Induction of epithelial to mesenchymal transition in PMC42-LA human breast carcinoma cells by carcinoma-associated fibroblast secreted factors | Breast Cancer Research
Description:
Background Breast carcinoma is accompanied by changes in the acellular and cellular components of the microenvironment, the latter typified by a switch from fibroblasts to myofibroblasts. Methods We utilised conditioned media cultures, Western blot analysis and immunocytochemistry to investigate the differential effects of normal mammary fibroblasts (NMFs) and mammary cancer-associated fibroblasts (CAFs) on the phenotype and behaviour of PMC42-LA breast cancer cells. NMFs were obtained from a mammary gland at reduction mammoplasty, and CAFs from a mammary carcinoma after resection. Results We found greater expression of myofibroblastic markers in CAFs than in NMFs. Medium from both CAFs and NMFs induced novel expression of α-smooth muscle actin and cytokeratin-14 in PMC42-LA organoids. However, although conditioned media from NMFs resulted in distribution of vimentin-positive cells to the periphery of PMC42-LA organoids, this was not seen with CAF-conditioned medium. Upregulation of vimentin was accompanied by a mis-localization of E-cadherin, suggesting a loss of adhesive function. This was confirmed by visualizing the change in active β-catenin, localized to the cell junctions in control cells/cells in NMF-conditioned medium, to inactive β-catenin, localized to nuclei and cytoplasm in cells in CAF-conditioned medium. Conclusion We found no significant difference between the influences of NMFs and CAFs on PMC42-LA cell proliferation, viability, or apoptosis; significantly, we demonstrated a role for CAFs, but not for NMFs, in increasing the migratory ability of PMC42-LA cells. By concentrating NMF-conditioned media, we demonstrated the presence of factor(s) that induce epithelial-mesenchymal transition in NMF-conditioned media that are present at higher levels in CAF-conditioned media. Our in vitro results are consistent with observations in vivo showing that alterations in stroma influence the phenotype and behaviour of surrounding cells and provide evidence for a role for CAFs in stimulating cancer progression via an epithelial-mesenchymal transition. These findings have implications for our understanding of the roles of signalling between epithelial and stromal cells in the development and progression of mammary carcinoma.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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Keywords {🔍}

cells, medium, pmcla, cell, pubmed, fibroblasts, breast, cancer, cafs, google, scholar, cas, nmfs, figure, article, expression, mammary, cultured, cafconditioned, hours, organoids, nmfconditioned, fibroblast, vimentin, human, ecadherin, control, growth, media, wound, epithelial, normal, filter, carcinoma, factors, beneath, cultures, culture, emt, conditioned, compared, increase, res, tissue, protein, part, presence, fold, factor, usa,

Topics {✒️}

beta-catenin/lef-1-mediated transactivation goat anti-human e-cadherin chemically-induced colo-rectal carcinogenesis enzyme-linked immunosorbent assay mouse anti-human vimentin article download pdf α-sma-positive stromal cells caf-conditioned media e-cadherin anti-human fap antibodies breast carcinoma metastasis cell-cell adhesion molecule induce epithelial-mesenchymal transition reduction mammoplasty tissue anti-human catenin-β tumour necrosis factor-α caf-conditioned medium induces e-cadherin mediates adhesion caf-conditioned medium exhibited cell-adhesion-dependent influences nmf-conditioned media enhances nmf-conditioned medium exhibited α-smooth muscle actin human breast-cancer cells reactive-tumour stromal cells pmc42-la organoids exhibited pmc42-la monolayers cultured concentrating nmf-conditioned media pmc42-la cell cultures caf-conditioned medium appeared breast fibroblast-conditioned medium smooth-muscle stromal cells smooth muscle-specific proteins full size image concentrated nmf-conditioned media casein/tris-buffered saline pmc42-la monolayer cultures pmc42-la monolayer cells stray pmc42-la cells pmc42-la cell proliferation α-sma-expressing cells vimentin-positive cells layered pmc42-la organoid morphology pmc42-la cells cultured culture pmc42-la cells e-cadherin expression correlates e-cadherin expressing cells epithelial-mesenchymal transition 2-dimensional pmc42-la culture bovine serum albumin/pbs pmc42-la cell wounds

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Induction of epithelial to mesenchymal transition in PMC42-LA human breast carcinoma cells by carcinoma-associated fibroblast secreted factors
         description:Breast carcinoma is accompanied by changes in the acellular and cellular components of the microenvironment, the latter typified by a switch from fibroblasts to myofibroblasts. We utilised conditioned media cultures, Western blot analysis and immunocytochemistry to investigate the differential effects of normal mammary fibroblasts (NMFs) and mammary cancer-associated fibroblasts (CAFs) on the phenotype and behaviour of PMC42-LA breast cancer cells. NMFs were obtained from a mammary gland at reduction mammoplasty, and CAFs from a mammary carcinoma after resection. We found greater expression of myofibroblastic markers in CAFs than in NMFs. Medium from both CAFs and NMFs induced novel expression of α-smooth muscle actin and cytokeratin-14 in PMC42-LA organoids. However, although conditioned media from NMFs resulted in distribution of vimentin-positive cells to the periphery of PMC42-LA organoids, this was not seen with CAF-conditioned medium. Upregulation of vimentin was accompanied by a mis-localization of E-cadherin, suggesting a loss of adhesive function. This was confirmed by visualizing the change in active β-catenin, localized to the cell junctions in control cells/cells in NMF-conditioned medium, to inactive β-catenin, localized to nuclei and cytoplasm in cells in CAF-conditioned medium. We found no significant difference between the influences of NMFs and CAFs on PMC42-LA cell proliferation, viability, or apoptosis; significantly, we demonstrated a role for CAFs, but not for NMFs, in increasing the migratory ability of PMC42-LA cells. By concentrating NMF-conditioned media, we demonstrated the presence of factor(s) that induce epithelial-mesenchymal transition in NMF-conditioned media that are present at higher levels in CAF-conditioned media. Our in vitro results are consistent with observations in vivo showing that alterations in stroma influence the phenotype and behaviour of surrounding cells and provide evidence for a role for CAFs in stimulating cancer progression via an epithelial-mesenchymal transition. These findings have implications for our understanding of the roles of signalling between epithelial and stromal cells in the development and progression of mammary carcinoma.
         datePublished:2007-02-20T00:00:00Z
         dateModified:2007-02-20T00:00:00Z
         pageStart:1
         pageEnd:15
         license:http://creativecommons.org/licenses/by/2.0/
         sameAs:https://doi.org/10.1186/bcr1656
         keywords:
            Conditioned Medium
            Vimentin Expression
            Fibroblast Activation Protein
            Reduction Mammoplasty
            Myoepithelial Marker
            Cancer Research
            Oncology
            Surgical Oncology
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            issn:
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               name:Stephanie C Lebret
               affiliation:
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                     address:
                        name:Deakin University, Burwood, Australia
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Donald F Newgreen
               affiliation:
                     name:The Murdoch Children's Research Institute
                     address:
                        name:The Murdoch Children's Research Institute, Parkville, Australia
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Erik W Thompson
               affiliation:
                     name:University of Melbourne
                     address:
                        name:Department of Surgery, University of Melbourne, Parkville, Australia
                        type:PostalAddress
                     type:Organization
                     name:Victoria Parade
                     address:
                        name:St. Vincent's Institute of Medical Research, Victoria Parade, Fitzroy, Australia
                        type:PostalAddress
                     type:Organization
                     name:Bernard O'Brien Institute for Microsurgery
                     address:
                        name:Bernard O'Brien Institute for Microsurgery, Fitzroy, Australia
                        type:PostalAddress
                     type:Organization
               type:Person
               name:M Leigh Ackland
               affiliation:
                     name:Deakin University
                     address:
                        name:Deakin University, Burwood, Australia
                        type:PostalAddress
                     type:Organization
               email:[email protected]
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ScholarlyArticle:
      headline:Induction of epithelial to mesenchymal transition in PMC42-LA human breast carcinoma cells by carcinoma-associated fibroblast secreted factors
      description:Breast carcinoma is accompanied by changes in the acellular and cellular components of the microenvironment, the latter typified by a switch from fibroblasts to myofibroblasts. We utilised conditioned media cultures, Western blot analysis and immunocytochemistry to investigate the differential effects of normal mammary fibroblasts (NMFs) and mammary cancer-associated fibroblasts (CAFs) on the phenotype and behaviour of PMC42-LA breast cancer cells. NMFs were obtained from a mammary gland at reduction mammoplasty, and CAFs from a mammary carcinoma after resection. We found greater expression of myofibroblastic markers in CAFs than in NMFs. Medium from both CAFs and NMFs induced novel expression of α-smooth muscle actin and cytokeratin-14 in PMC42-LA organoids. However, although conditioned media from NMFs resulted in distribution of vimentin-positive cells to the periphery of PMC42-LA organoids, this was not seen with CAF-conditioned medium. Upregulation of vimentin was accompanied by a mis-localization of E-cadherin, suggesting a loss of adhesive function. This was confirmed by visualizing the change in active β-catenin, localized to the cell junctions in control cells/cells in NMF-conditioned medium, to inactive β-catenin, localized to nuclei and cytoplasm in cells in CAF-conditioned medium. We found no significant difference between the influences of NMFs and CAFs on PMC42-LA cell proliferation, viability, or apoptosis; significantly, we demonstrated a role for CAFs, but not for NMFs, in increasing the migratory ability of PMC42-LA cells. By concentrating NMF-conditioned media, we demonstrated the presence of factor(s) that induce epithelial-mesenchymal transition in NMF-conditioned media that are present at higher levels in CAF-conditioned media. Our in vitro results are consistent with observations in vivo showing that alterations in stroma influence the phenotype and behaviour of surrounding cells and provide evidence for a role for CAFs in stimulating cancer progression via an epithelial-mesenchymal transition. These findings have implications for our understanding of the roles of signalling between epithelial and stromal cells in the development and progression of mammary carcinoma.
      datePublished:2007-02-20T00:00:00Z
      dateModified:2007-02-20T00:00:00Z
      pageStart:1
      pageEnd:15
      license:http://creativecommons.org/licenses/by/2.0/
      sameAs:https://doi.org/10.1186/bcr1656
      keywords:
         Conditioned Medium
         Vimentin Expression
         Fibroblast Activation Protein
         Reduction Mammoplasty
         Myoepithelial Marker
         Cancer Research
         Oncology
         Surgical Oncology
      image:
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         name:Breast Cancer Research
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         volumeNumber:9
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         name:BioMed Central
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            type:ImageObject
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      author:
            name:Stephanie C Lebret
            affiliation:
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                  address:
                     name:Deakin University, Burwood, Australia
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Donald F Newgreen
            affiliation:
                  name:The Murdoch Children's Research Institute
                  address:
                     name:The Murdoch Children's Research Institute, Parkville, Australia
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Erik W Thompson
            affiliation:
                  name:University of Melbourne
                  address:
                     name:Department of Surgery, University of Melbourne, Parkville, Australia
                     type:PostalAddress
                  type:Organization
                  name:Victoria Parade
                  address:
                     name:St. Vincent's Institute of Medical Research, Victoria Parade, Fitzroy, Australia
                     type:PostalAddress
                  type:Organization
                  name:Bernard O'Brien Institute for Microsurgery
                  address:
                     name:Bernard O'Brien Institute for Microsurgery, Fitzroy, Australia
                     type:PostalAddress
                  type:Organization
            type:Person
            name:M Leigh Ackland
            affiliation:
                  name:Deakin University
                  address:
                     name:Deakin University, Burwood, Australia
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      isAccessibleForFree:1
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      name:Deakin University
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         name:Deakin University, Burwood, Australia
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      address:
         name:The Murdoch Children's Research Institute, Parkville, Australia
         type:PostalAddress
      name:University of Melbourne
      address:
         name:Department of Surgery, University of Melbourne, Parkville, Australia
         type:PostalAddress
      name:Victoria Parade
      address:
         name:St. Vincent's Institute of Medical Research, Victoria Parade, Fitzroy, Australia
         type:PostalAddress
      name:Bernard O'Brien Institute for Microsurgery
      address:
         name:Bernard O'Brien Institute for Microsurgery, Fitzroy, Australia
         type:PostalAddress
      name:Deakin University
      address:
         name:Deakin University, Burwood, Australia
         type:PostalAddress
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Person:
      name:Stephanie C Lebret
      affiliation:
            name:Deakin University
            address:
               name:Deakin University, Burwood, Australia
               type:PostalAddress
            type:Organization
      name:Donald F Newgreen
      affiliation:
            name:The Murdoch Children's Research Institute
            address:
               name:The Murdoch Children's Research Institute, Parkville, Australia
               type:PostalAddress
            type:Organization
      name:Erik W Thompson
      affiliation:
            name:University of Melbourne
            address:
               name:Department of Surgery, University of Melbourne, Parkville, Australia
               type:PostalAddress
            type:Organization
            name:Victoria Parade
            address:
               name:St. Vincent's Institute of Medical Research, Victoria Parade, Fitzroy, Australia
               type:PostalAddress
            type:Organization
            name:Bernard O'Brien Institute for Microsurgery
            address:
               name:Bernard O'Brien Institute for Microsurgery, Fitzroy, Australia
               type:PostalAddress
            type:Organization
      name:M Leigh Ackland
      affiliation:
            name:Deakin University
            address:
               name:Deakin University, Burwood, Australia
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Deakin University, Burwood, Australia
      name:The Murdoch Children's Research Institute, Parkville, Australia
      name:Department of Surgery, University of Melbourne, Parkville, Australia
      name:St. Vincent's Institute of Medical Research, Victoria Parade, Fitzroy, Australia
      name:Bernard O'Brien Institute for Microsurgery, Fitzroy, Australia
      name:Deakin University, Burwood, Australia

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