Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer

Approximately 25,000 ovarian cancers are diagnosed in the U.S. annually, and 75% are in the advanced stage and largely incurable. There is critical need for early detection tools and novel treatments. Proteasomal ubiquitin receptor ADRM1 is a protein that is encoded by the ADRM1 gene. Recently, we s...

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Main Authors: Dennis J. Slamon, Richard S. Finn, Gottfried E. Konecny, Michael J. Haykinson, Nuraly K. Avliyakulov, Ondrej Kalous, Erika M. von Euw, Lee Anderson, Marlena S. Fejzo
Format: Article
Language:English
Published: MDPI AG 2013-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/14/2/3094
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spelling doaj-e6a81a305eb5421c9d51437d354378582020-11-24T20:44:29ZengMDPI AGInternational Journal of Molecular Sciences1422-00672013-02-011423094310910.3390/ijms14023094Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian CancerDennis J. SlamonRichard S. FinnGottfried E. KonecnyMichael J. HaykinsonNuraly K. AvliyakulovOndrej KalousErika M. von EuwLee AndersonMarlena S. FejzoApproximately 25,000 ovarian cancers are diagnosed in the U.S. annually, and 75% are in the advanced stage and largely incurable. There is critical need for early detection tools and novel treatments. Proteasomal ubiquitin receptor ADRM1 is a protein that is encoded by the ADRM1 gene. Recently, we showed that among 20q13-amplified genes in ovarian cancer, ADRM1 overexpression was the most highly correlated with amplification and was significantly upregulated with respect to stage, recurrence, and metastasis. Its overexpression correlated significantly with shorter time to recurrence and overall survival. Array-CGH and microarray expression of ovarian cancer cell lines provided evidence consistent with primary tumor data that ADRM1 is a 20q13 amplification target. Herein, we confirm the ADRM1 amplicon in a second ovarian cancer cohort and define a minimally amplified region of 262 KB encompassing seven genes. Additionally, using RNAi knock-down of ADRM1 in naturally amplified cell line OAW42 and overexpression of ADRM1 via transfection in ES2, we show that (1) ADRM1 overexpression increases proliferation, migration, and growth in soft agar, and (2) knock-down of ADRM1 results in apoptosis. Proteomic analysis of cells with ADRM1 knock-down reveals dysregulation of proteins including CDK-activating kinase assembly factor MAT1. Taken together, the results indicate that amplified ADRM1 is involved in cell proliferation, migration and survival in ovarian cancer cells, supporting a role as an oncogene and novel therapeutic target for ovarian cancer.http://www.mdpi.com/1422-0067/14/2/3094ADRM1oncogeneovarian cancer
collection DOAJ
language English
format Article
sources DOAJ
author Dennis J. Slamon
Richard S. Finn
Gottfried E. Konecny
Michael J. Haykinson
Nuraly K. Avliyakulov
Ondrej Kalous
Erika M. von Euw
Lee Anderson
Marlena S. Fejzo
spellingShingle Dennis J. Slamon
Richard S. Finn
Gottfried E. Konecny
Michael J. Haykinson
Nuraly K. Avliyakulov
Ondrej Kalous
Erika M. von Euw
Lee Anderson
Marlena S. Fejzo
Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer
International Journal of Molecular Sciences
ADRM1
oncogene
ovarian cancer
author_facet Dennis J. Slamon
Richard S. Finn
Gottfried E. Konecny
Michael J. Haykinson
Nuraly K. Avliyakulov
Ondrej Kalous
Erika M. von Euw
Lee Anderson
Marlena S. Fejzo
author_sort Dennis J. Slamon
title Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer
title_short Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer
title_full Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer
title_fullStr Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer
title_full_unstemmed Amplification Target ADRM1: Role as an Oncogene and Therapeutic Target for Ovarian Cancer
title_sort amplification target adrm1: role as an oncogene and therapeutic target for ovarian cancer
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2013-02-01
description Approximately 25,000 ovarian cancers are diagnosed in the U.S. annually, and 75% are in the advanced stage and largely incurable. There is critical need for early detection tools and novel treatments. Proteasomal ubiquitin receptor ADRM1 is a protein that is encoded by the ADRM1 gene. Recently, we showed that among 20q13-amplified genes in ovarian cancer, ADRM1 overexpression was the most highly correlated with amplification and was significantly upregulated with respect to stage, recurrence, and metastasis. Its overexpression correlated significantly with shorter time to recurrence and overall survival. Array-CGH and microarray expression of ovarian cancer cell lines provided evidence consistent with primary tumor data that ADRM1 is a 20q13 amplification target. Herein, we confirm the ADRM1 amplicon in a second ovarian cancer cohort and define a minimally amplified region of 262 KB encompassing seven genes. Additionally, using RNAi knock-down of ADRM1 in naturally amplified cell line OAW42 and overexpression of ADRM1 via transfection in ES2, we show that (1) ADRM1 overexpression increases proliferation, migration, and growth in soft agar, and (2) knock-down of ADRM1 results in apoptosis. Proteomic analysis of cells with ADRM1 knock-down reveals dysregulation of proteins including CDK-activating kinase assembly factor MAT1. Taken together, the results indicate that amplified ADRM1 is involved in cell proliferation, migration and survival in ovarian cancer cells, supporting a role as an oncogene and novel therapeutic target for ovarian cancer.
topic ADRM1
oncogene
ovarian cancer
url http://www.mdpi.com/1422-0067/14/2/3094
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