The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.

Ecotropic viral integration site-1 (EVI1) is one of the candidate oncogenes for human acute myeloid leukemia (AML) with chromosomal alterations at 3q26. High EVI1 expression (EVI1(high)) is a risk factor for AML with poor outcome. Using DNA microarray analysis, we previously identified that integrin...

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Autores principales: Norio Yamakawa, Kazuko Kaneda, Yusuke Saito, Emi Ichihara, Kazuhiro Morishita
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:a2f90864bbf54dcfa024ff6935b273d82021-11-18T07:29:20ZThe increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.1932-620310.1371/journal.pone.0030706https://doaj.org/article/a2f90864bbf54dcfa024ff6935b273d82012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22295105/?tool=EBIhttps://doaj.org/toc/1932-6203Ecotropic viral integration site-1 (EVI1) is one of the candidate oncogenes for human acute myeloid leukemia (AML) with chromosomal alterations at 3q26. High EVI1 expression (EVI1(high)) is a risk factor for AML with poor outcome. Using DNA microarray analysis, we previously identified that integrin α6 (ITGA6) was upregulated over 10-fold in EVI1(high) leukemia cells. In this study, we determined whether the increased expression of ITGA6 is associated with drug-resistance and increased cell adhesion, resulting in poor prognosis. To this end, we first confirmed the expression pattern of a series of integrin genes using semi-quantitative PCR and fluorescence-activated cell sorter (FACS) analysis and determined the cell adhesion ability in EVI1(high) leukemia cells. We found that the adhesion ability of EVI1(high) leukemia cells to laminin increased with the increased expression of ITGA6 and integrin β4 (ITGB4). The introduction of small-hairpin RNA against EVI1 (shEVI1) into EVI1(high) leukemia cells reduced the cell adhesion ability and downregulated the expression of ITGA6 and ITGB4. In addition, the overexpression of EVI1 in EVI1(low) leukemia cells enhanced their cell adhesion ability and increased the expression of ITGA6 and ITGB4. In a subsequent experiment, the introduction of shRNA against ITGA6 or ITGB4 into EVI1(high) AML cells downregulated their cell adhesion ability; however, the EVI1(high) AML cells transfected with shRNA against ITGA6 could not be maintained in culture. Moreover, treating EVI1(high) leukemia cells with neutralizing antibodies against ITGA6 or ITGB4 resulted in an enhanced responsiveness to anti-cancer drugs and a reduction of their cell adhesion ability. The expression of ITGA6 is significantly elevated in cells from relapsed and EVI1(high) AML cases; therefore, ITGA6 might represent an important therapeutic target for both refractory and EVI1(high) AML.Norio YamakawaKazuko KanedaYusuke SaitoEmi IchiharaKazuhiro MorishitaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 1, p e30706 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Norio Yamakawa
Kazuko Kaneda
Yusuke Saito
Emi Ichihara
Kazuhiro Morishita
The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.
description Ecotropic viral integration site-1 (EVI1) is one of the candidate oncogenes for human acute myeloid leukemia (AML) with chromosomal alterations at 3q26. High EVI1 expression (EVI1(high)) is a risk factor for AML with poor outcome. Using DNA microarray analysis, we previously identified that integrin α6 (ITGA6) was upregulated over 10-fold in EVI1(high) leukemia cells. In this study, we determined whether the increased expression of ITGA6 is associated with drug-resistance and increased cell adhesion, resulting in poor prognosis. To this end, we first confirmed the expression pattern of a series of integrin genes using semi-quantitative PCR and fluorescence-activated cell sorter (FACS) analysis and determined the cell adhesion ability in EVI1(high) leukemia cells. We found that the adhesion ability of EVI1(high) leukemia cells to laminin increased with the increased expression of ITGA6 and integrin β4 (ITGB4). The introduction of small-hairpin RNA against EVI1 (shEVI1) into EVI1(high) leukemia cells reduced the cell adhesion ability and downregulated the expression of ITGA6 and ITGB4. In addition, the overexpression of EVI1 in EVI1(low) leukemia cells enhanced their cell adhesion ability and increased the expression of ITGA6 and ITGB4. In a subsequent experiment, the introduction of shRNA against ITGA6 or ITGB4 into EVI1(high) AML cells downregulated their cell adhesion ability; however, the EVI1(high) AML cells transfected with shRNA against ITGA6 could not be maintained in culture. Moreover, treating EVI1(high) leukemia cells with neutralizing antibodies against ITGA6 or ITGB4 resulted in an enhanced responsiveness to anti-cancer drugs and a reduction of their cell adhesion ability. The expression of ITGA6 is significantly elevated in cells from relapsed and EVI1(high) AML cases; therefore, ITGA6 might represent an important therapeutic target for both refractory and EVI1(high) AML.
format article
author Norio Yamakawa
Kazuko Kaneda
Yusuke Saito
Emi Ichihara
Kazuhiro Morishita
author_facet Norio Yamakawa
Kazuko Kaneda
Yusuke Saito
Emi Ichihara
Kazuhiro Morishita
author_sort Norio Yamakawa
title The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.
title_short The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.
title_full The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.
title_fullStr The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.
title_full_unstemmed The increased expression of integrin α6 (ITGA6) enhances drug resistance in EVI1(high) leukemia.
title_sort increased expression of integrin α6 (itga6) enhances drug resistance in evi1(high) leukemia.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/a2f90864bbf54dcfa024ff6935b273d8
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