Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells

Acquisition of invasive/metastatic potential is a key event in tumor progression. Cell surface glycoproteins and their respective matrix ligands have been implicated in this process. Recent evidence reveals that the secreted glycoprotein SPARC (secreted protein, acidic and rich in cysteine) is highl...

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Autores principales: Fernanda Ledda, M., Adris, S., Bravo, A.I., Kairiyama, C., Bover, L., Chernajovsky, Y., Mordoh, J., Podhajcer, O.L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_10788956_v3_n2_p171_FernandaLedda
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spelling todo:paper_10788956_v3_n2_p171_FernandaLedda2023-10-03T16:03:42Z Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells Fernanda Ledda, M. Adris, S. Bravo, A.I. Kairiyama, C. Bover, L. Chernajovsky, Y. Mordoh, J. Podhajcer, O.L. complementary rna glycoprotein osteonectin animal experiment article cancer inhibition cancer invasion controlled study human human cell melanoma cell metastasis mouse nonhuman priority journal Animals Cell Adhesion Cell Division Cell Movement Down-Regulation Gene Expression Regulation, Neoplastic Humans Melanoma Melanoma, Experimental Mice Oligonucleotides, Antisense Osteonectin Transfection Tumor Cells, Cultured Animalia Acquisition of invasive/metastatic potential is a key event in tumor progression. Cell surface glycoproteins and their respective matrix ligands have been implicated in this process. Recent evidence reveals that the secreted glycoprotein SPARC (secreted protein, acidic and rich in cysteine) is highly expressed in different malignant tissues. The present study reports that the suppression of SPARC expression by human melanoma cells using a SPARC antisense expression vector results in a significant decrease in the in vitro adhesive and invasive capacities of tumor cells, completely abolishing their in vivo tumorigenicity. This is the first evidence that SPARC plays a key role in human melanoma invasive-metastatic phenotype development. Fil:Fernanda Ledda, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bover, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Podhajcer, O.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_10788956_v3_n2_p171_FernandaLedda
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic complementary rna
glycoprotein
osteonectin
animal experiment
article
cancer inhibition
cancer invasion
controlled study
human
human cell
melanoma cell
metastasis
mouse
nonhuman
priority journal
Animals
Cell Adhesion
Cell Division
Cell Movement
Down-Regulation
Gene Expression Regulation, Neoplastic
Humans
Melanoma
Melanoma, Experimental
Mice
Oligonucleotides, Antisense
Osteonectin
Transfection
Tumor Cells, Cultured
Animalia
spellingShingle complementary rna
glycoprotein
osteonectin
animal experiment
article
cancer inhibition
cancer invasion
controlled study
human
human cell
melanoma cell
metastasis
mouse
nonhuman
priority journal
Animals
Cell Adhesion
Cell Division
Cell Movement
Down-Regulation
Gene Expression Regulation, Neoplastic
Humans
Melanoma
Melanoma, Experimental
Mice
Oligonucleotides, Antisense
Osteonectin
Transfection
Tumor Cells, Cultured
Animalia
Fernanda Ledda, M.
Adris, S.
Bravo, A.I.
Kairiyama, C.
Bover, L.
Chernajovsky, Y.
Mordoh, J.
Podhajcer, O.L.
Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells
topic_facet complementary rna
glycoprotein
osteonectin
animal experiment
article
cancer inhibition
cancer invasion
controlled study
human
human cell
melanoma cell
metastasis
mouse
nonhuman
priority journal
Animals
Cell Adhesion
Cell Division
Cell Movement
Down-Regulation
Gene Expression Regulation, Neoplastic
Humans
Melanoma
Melanoma, Experimental
Mice
Oligonucleotides, Antisense
Osteonectin
Transfection
Tumor Cells, Cultured
Animalia
description Acquisition of invasive/metastatic potential is a key event in tumor progression. Cell surface glycoproteins and their respective matrix ligands have been implicated in this process. Recent evidence reveals that the secreted glycoprotein SPARC (secreted protein, acidic and rich in cysteine) is highly expressed in different malignant tissues. The present study reports that the suppression of SPARC expression by human melanoma cells using a SPARC antisense expression vector results in a significant decrease in the in vitro adhesive and invasive capacities of tumor cells, completely abolishing their in vivo tumorigenicity. This is the first evidence that SPARC plays a key role in human melanoma invasive-metastatic phenotype development.
format JOUR
author Fernanda Ledda, M.
Adris, S.
Bravo, A.I.
Kairiyama, C.
Bover, L.
Chernajovsky, Y.
Mordoh, J.
Podhajcer, O.L.
author_facet Fernanda Ledda, M.
Adris, S.
Bravo, A.I.
Kairiyama, C.
Bover, L.
Chernajovsky, Y.
Mordoh, J.
Podhajcer, O.L.
author_sort Fernanda Ledda, M.
title Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells
title_short Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells
title_full Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells
title_fullStr Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells
title_full_unstemmed Suppression of SPARC expression by antisense RNA abrogates the tumorigenicity of human melanoma cells
title_sort suppression of sparc expression by antisense rna abrogates the tumorigenicity of human melanoma cells
url http://hdl.handle.net/20.500.12110/paper_10788956_v3_n2_p171_FernandaLedda
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