Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells

Silencing of fibronectin (FN) expression seems to be one of the key mechanisms underlying metastatic behaviour. An inverse correlation exists between FN expression levels and the metastatic potential of two related murine mammary adenocarcinomas, M3 and MM3. Primary cultures of M3 tumour, which is m...

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Autores principales: Werbajh, S.E., Urtreger, A.J., Puricelli, L.I., De Lustig, E.S., Bal De Kier Joffé, E., Kornblihtt, A.R.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00145793_v440_n3_p277_Werbajh
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spelling todo:paper_00145793_v440_n3_p277_Werbajh2023-10-03T14:13:05Z Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells Werbajh, S.E. Urtreger, A.J. Puricelli, L.I. De Lustig, E.S. Bal De Kier Joffé, E. Kornblihtt, A.R. Fibronectin Metastasis Transcription fibronectin messenger RNA article breast adenocarcinoma human human cell lung metastasis metastasis potential priority journal promoter region protein expression RNA transcription single strand conformation polymorphism Murinae Silencing of fibronectin (FN) expression seems to be one of the key mechanisms underlying metastatic behaviour. An inverse correlation exists between FN expression levels and the metastatic potential of two related murine mammary adenocarcinomas, M3 and MM3. Primary cultures of M3 tumour, which is moderately metastatic to lung (40% incidence), show a conspicuous FN extracellular matrix (ECM) and high levels of FN mRNA, while primary cultures of the highly metastatic MM3 tumour (95% lung incidence) are negative for FN in immunofluorescence and show at least 40-fold lower levels of FN mRNA, only detectable by RT-PCR, with a different pattern of alternatively spliced EDI isoforms compared to M3 cells. We show that the FN promoter sequence is not altered in MM3 cells. Transfection experiments with CAT constructs indicate that silencing occurs at the transcriptional level, involving the 220-bp proximal promoter region. Copyright (C) 1998 Federation of European Biochemical Societies. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00145793_v440_n3_p277_Werbajh
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Fibronectin
Metastasis
Transcription
fibronectin
messenger RNA
article
breast adenocarcinoma
human
human cell
lung metastasis
metastasis potential
priority journal
promoter region
protein expression
RNA transcription
single strand conformation polymorphism
Murinae
spellingShingle Fibronectin
Metastasis
Transcription
fibronectin
messenger RNA
article
breast adenocarcinoma
human
human cell
lung metastasis
metastasis potential
priority journal
promoter region
protein expression
RNA transcription
single strand conformation polymorphism
Murinae
Werbajh, S.E.
Urtreger, A.J.
Puricelli, L.I.
De Lustig, E.S.
Bal De Kier Joffé, E.
Kornblihtt, A.R.
Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
topic_facet Fibronectin
Metastasis
Transcription
fibronectin
messenger RNA
article
breast adenocarcinoma
human
human cell
lung metastasis
metastasis potential
priority journal
promoter region
protein expression
RNA transcription
single strand conformation polymorphism
Murinae
description Silencing of fibronectin (FN) expression seems to be one of the key mechanisms underlying metastatic behaviour. An inverse correlation exists between FN expression levels and the metastatic potential of two related murine mammary adenocarcinomas, M3 and MM3. Primary cultures of M3 tumour, which is moderately metastatic to lung (40% incidence), show a conspicuous FN extracellular matrix (ECM) and high levels of FN mRNA, while primary cultures of the highly metastatic MM3 tumour (95% lung incidence) are negative for FN in immunofluorescence and show at least 40-fold lower levels of FN mRNA, only detectable by RT-PCR, with a different pattern of alternatively spliced EDI isoforms compared to M3 cells. We show that the FN promoter sequence is not altered in MM3 cells. Transfection experiments with CAT constructs indicate that silencing occurs at the transcriptional level, involving the 220-bp proximal promoter region. Copyright (C) 1998 Federation of European Biochemical Societies.
format JOUR
author Werbajh, S.E.
Urtreger, A.J.
Puricelli, L.I.
De Lustig, E.S.
Bal De Kier Joffé, E.
Kornblihtt, A.R.
author_facet Werbajh, S.E.
Urtreger, A.J.
Puricelli, L.I.
De Lustig, E.S.
Bal De Kier Joffé, E.
Kornblihtt, A.R.
author_sort Werbajh, S.E.
title Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
title_short Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
title_full Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
title_fullStr Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
title_full_unstemmed Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
title_sort downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells
url http://hdl.handle.net/20.500.12110/paper_00145793_v440_n3_p277_Werbajh
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AT urtregeraj downregulationoffibronectintranscriptioninhighlymetastaticadenocarcinomacells
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AT delustiges downregulationoffibronectintranscriptioninhighlymetastaticadenocarcinomacells
AT baldekierjoffee downregulationoffibronectintranscriptioninhighlymetastaticadenocarcinomacells
AT kornblihttar downregulationoffibronectintranscriptioninhighlymetastaticadenocarcinomacells
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