DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.

CD44 adhesion molecules are expressed in many breast cancer cells and have been demonstrated to play a key role in regulating malignant phenotypes such as growth, migration, and invasion. CD44 is an integral transmembrane protein encoded by a single 20-exon gene. The diversity of the biological func...

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Main Authors: Joji Iida, Rebecca Clancy, Jesse Dorchak, Richard I Somiari, Stella Somiari, Mary Lou Cutler, Richard J Mural, Craig D Shriver
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3929491?pdf=render
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spelling doaj-e8e84955464b40e9945892eca7b0a9e52020-11-25T00:47:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8871210.1371/journal.pone.0088712DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.Joji IidaRebecca ClancyJesse DorchakRichard I SomiariStella SomiariMary Lou CutlerRichard J MuralCraig D ShriverCD44 adhesion molecules are expressed in many breast cancer cells and have been demonstrated to play a key role in regulating malignant phenotypes such as growth, migration, and invasion. CD44 is an integral transmembrane protein encoded by a single 20-exon gene. The diversity of the biological functions of CD44 is the result of the various splicing variants of these exons. Previous studies suggest that exon v10 of CD44 plays a key role in promoting cancer invasion and metastasis, however, the molecular mechanisms are not clear. Given the fact that exon v10 is in the ectodomain of CD44, we hypothesized that CD44 forms a molecular complex with other cell surface molecules through exon v10 in order to promote migration of breast cancer cells. In order to test this hypothesis, we selected DNA aptamers that specifically bound to CD44 exon v10 using Systematic Evolution of Ligands by Exponential Enrichment (SELEX). We selected aptamers that inhibited migration of breast cancer cells. Co-immunoprecipitation studies demonstrated that EphA2 was co-precipitated with CD44. Pull-down studies demonstrated that recombinant CD44 exon v10 bound to EphA2 and more importantly aptamers that inhibited migration also prevented the binding of EphA2 to exon v10. These results suggest that CD44 forms a molecular complex with EphA2 on the breast cancer cell surface and this complex plays a key role in enhancing breast cancer migration. These results provide insight not only for characterizing mechanisms of breast cancer migration but also for developing target-specific therapy for breast cancers and possibly other cancer types expressing CD44 exon v10.http://europepmc.org/articles/PMC3929491?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Joji Iida
Rebecca Clancy
Jesse Dorchak
Richard I Somiari
Stella Somiari
Mary Lou Cutler
Richard J Mural
Craig D Shriver
spellingShingle Joji Iida
Rebecca Clancy
Jesse Dorchak
Richard I Somiari
Stella Somiari
Mary Lou Cutler
Richard J Mural
Craig D Shriver
DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.
PLoS ONE
author_facet Joji Iida
Rebecca Clancy
Jesse Dorchak
Richard I Somiari
Stella Somiari
Mary Lou Cutler
Richard J Mural
Craig D Shriver
author_sort Joji Iida
title DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.
title_short DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.
title_full DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.
title_fullStr DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.
title_full_unstemmed DNA aptamers against exon v10 of CD44 inhibit breast cancer cell migration.
title_sort dna aptamers against exon v10 of cd44 inhibit breast cancer cell migration.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description CD44 adhesion molecules are expressed in many breast cancer cells and have been demonstrated to play a key role in regulating malignant phenotypes such as growth, migration, and invasion. CD44 is an integral transmembrane protein encoded by a single 20-exon gene. The diversity of the biological functions of CD44 is the result of the various splicing variants of these exons. Previous studies suggest that exon v10 of CD44 plays a key role in promoting cancer invasion and metastasis, however, the molecular mechanisms are not clear. Given the fact that exon v10 is in the ectodomain of CD44, we hypothesized that CD44 forms a molecular complex with other cell surface molecules through exon v10 in order to promote migration of breast cancer cells. In order to test this hypothesis, we selected DNA aptamers that specifically bound to CD44 exon v10 using Systematic Evolution of Ligands by Exponential Enrichment (SELEX). We selected aptamers that inhibited migration of breast cancer cells. Co-immunoprecipitation studies demonstrated that EphA2 was co-precipitated with CD44. Pull-down studies demonstrated that recombinant CD44 exon v10 bound to EphA2 and more importantly aptamers that inhibited migration also prevented the binding of EphA2 to exon v10. These results suggest that CD44 forms a molecular complex with EphA2 on the breast cancer cell surface and this complex plays a key role in enhancing breast cancer migration. These results provide insight not only for characterizing mechanisms of breast cancer migration but also for developing target-specific therapy for breast cancers and possibly other cancer types expressing CD44 exon v10.
url http://europepmc.org/articles/PMC3929491?pdf=render
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