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Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion
Regulation of the actin cytoskeleton may play a crucial role in cell motility and cancer invasion. We have produced a monoclonal antibody (NCC- Lu-632, IgM, k) reactive with an antigenic protein that is upregulated upon enhanced cell movement. The cDNA for the antigen molecule was found to encode a...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132673/ https://www.ncbi.nlm.nih.gov/pubmed/9508771 |
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author | Honda, Kazufumi Yamada, Tesshi Endo, Ritsuko Ino, Yoshinori Gotoh, Masahiro Tsuda, Hitoshi Yamada, Yozo Chiba, Hiroshige Hirohashi, Setsuo |
author_facet | Honda, Kazufumi Yamada, Tesshi Endo, Ritsuko Ino, Yoshinori Gotoh, Masahiro Tsuda, Hitoshi Yamada, Yozo Chiba, Hiroshige Hirohashi, Setsuo |
author_sort | Honda, Kazufumi |
collection | PubMed |
description | Regulation of the actin cytoskeleton may play a crucial role in cell motility and cancer invasion. We have produced a monoclonal antibody (NCC- Lu-632, IgM, k) reactive with an antigenic protein that is upregulated upon enhanced cell movement. The cDNA for the antigen molecule was found to encode a novel isoform of nonmuscle α-actinin. This isoform (designated actinin-4) was concentrated in the cytoplasm where cells were sharply extended and in cells migrating and located at the edge of cell clusters, but was absent from focal adhesion plaques or adherens junctions, where the classic isoform (actinin-1) was concentrated. Actinin-4 shifted steadily from the cytoplasm to the nucleus upon inhibition of phosphatidylinositol 3 kinase or actin depolymerization. The cytoplasmic localization of actinin-4 was closely associated with an infiltrative histological phenotype and correlated significantly with a poorer prognosis in 61 cases of breast cancer. These findings suggest that cytoplasmic actinin-4 regulates the actin cytoskeleton and increases cellular motility and that its inactivation by transfer to the nucleus abolishes the metastatic potential of human cancers. |
format | Text |
id | pubmed-2132673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21326732008-05-01 Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion Honda, Kazufumi Yamada, Tesshi Endo, Ritsuko Ino, Yoshinori Gotoh, Masahiro Tsuda, Hitoshi Yamada, Yozo Chiba, Hiroshige Hirohashi, Setsuo J Cell Biol Article Regulation of the actin cytoskeleton may play a crucial role in cell motility and cancer invasion. We have produced a monoclonal antibody (NCC- Lu-632, IgM, k) reactive with an antigenic protein that is upregulated upon enhanced cell movement. The cDNA for the antigen molecule was found to encode a novel isoform of nonmuscle α-actinin. This isoform (designated actinin-4) was concentrated in the cytoplasm where cells were sharply extended and in cells migrating and located at the edge of cell clusters, but was absent from focal adhesion plaques or adherens junctions, where the classic isoform (actinin-1) was concentrated. Actinin-4 shifted steadily from the cytoplasm to the nucleus upon inhibition of phosphatidylinositol 3 kinase or actin depolymerization. The cytoplasmic localization of actinin-4 was closely associated with an infiltrative histological phenotype and correlated significantly with a poorer prognosis in 61 cases of breast cancer. These findings suggest that cytoplasmic actinin-4 regulates the actin cytoskeleton and increases cellular motility and that its inactivation by transfer to the nucleus abolishes the metastatic potential of human cancers. The Rockefeller University Press 1998-03-23 /pmc/articles/PMC2132673/ /pubmed/9508771 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Honda, Kazufumi Yamada, Tesshi Endo, Ritsuko Ino, Yoshinori Gotoh, Masahiro Tsuda, Hitoshi Yamada, Yozo Chiba, Hiroshige Hirohashi, Setsuo Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion |
title | Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion |
title_full | Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion |
title_fullStr | Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion |
title_full_unstemmed | Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion |
title_short | Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion |
title_sort | actinin-4, a novel actin-bundling protein associated with cell motility and cancer invasion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132673/ https://www.ncbi.nlm.nih.gov/pubmed/9508771 |
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