Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer

Objective: The objective of this study is to identify and validate novel therapeutic target(s) in ovarian cancer. Background: Development of targeted therapeutics in ovarian cancer has been limited by molecular heterogeneity. Although gene expression datasets are available, most of them lack appropr...

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Main Authors: Michael A. Ulm, Tiffany M. Redfern, Ben R. Wilson, Suriyan Ponnusamy, Sarah Asemota, Patrick W. Blackburn, Yinan Wang, Adam C. ElNaggar, Ramesh Narayanan
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Journal of Personalized Medicine
Subjects:
Online Access:https://www.mdpi.com/2075-4426/10/4/246
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spelling doaj-fa0d6901fac44ded8f2f505488797dc52020-11-27T08:09:20ZengMDPI AGJournal of Personalized Medicine2075-44262020-11-011024624610.3390/jpm10040246Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian CancerMichael A. Ulm0Tiffany M. Redfern1Ben R. Wilson2Suriyan Ponnusamy3Sarah Asemota4Patrick W. Blackburn5Yinan Wang6Adam C. ElNaggar7Ramesh Narayanan8Division of Gynecologic Oncology, West Cancer Center and Research Institute, Memphis, TN 38138, USADivision of Gynecologic Oncology, West Cancer Center and Research Institute, Memphis, TN 38138, USADivision of Gynecologic Oncology, West Cancer Center and Research Institute, Memphis, TN 38138, USADepartment of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USADepartment of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USADivision of Gynecologic Oncology, West Cancer Center and Research Institute, Memphis, TN 38138, USADepartment of Pathology, University of Tennessee Health Science Center, Memphis, TN 38163, USADivision of Gynecologic Oncology, West Cancer Center and Research Institute, Memphis, TN 38138, USADepartment of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USAObjective: The objective of this study is to identify and validate novel therapeutic target(s) in ovarian cancer. Background: Development of targeted therapeutics in ovarian cancer has been limited by molecular heterogeneity. Although gene expression datasets are available, most of them lack appropriate pair-matched controls to define the alterations that result in the transformation of normal ovarian cells to cancerous cells. Methods: We used microarray to compare the gene expression of treatment-naïve ovarian cancer tissue samples to pair-matched normal adjacent ovarian tissue from 24 patients. Ingenuity Pathway Analysis (IPA) was used to identify target pathways for further analysis. Integrin-linked kinase (ILK) expression in SKOV3 and OV90 cells was determined using Western blot. ILK was knocked down using CRISPR/Cas9 constructs. Subcutaneous xenograft study to determine the effect of ILK knockdown on tumor growth was performed in NOD SCID gamma mice. Results: Significant upregulation of the ILK pathway was identified in 22 of the 24 cancer specimens, identifying it as a potential player that could contribute to the transformation of normal ovarian cells to cancerous cells. Knockdown of ILK in SKOV3 cells resulted in decreased cell proliferation and tumor growth, and inhibition of downstream kinase, AKT (protein kinase B). These results were further validated using an ILK-1 chemical inhibitor, compound 22. Conclusion: Our initial findings validate ILK as a potential therapeutic target for molecular inhibition in ovarian cancer, which warrants further investigation.https://www.mdpi.com/2075-4426/10/4/246integrin-linked kinase (ILK)ovarian cancersgRNAgene expressionmicroarrayxenograft
collection DOAJ
language English
format Article
sources DOAJ
author Michael A. Ulm
Tiffany M. Redfern
Ben R. Wilson
Suriyan Ponnusamy
Sarah Asemota
Patrick W. Blackburn
Yinan Wang
Adam C. ElNaggar
Ramesh Narayanan
spellingShingle Michael A. Ulm
Tiffany M. Redfern
Ben R. Wilson
Suriyan Ponnusamy
Sarah Asemota
Patrick W. Blackburn
Yinan Wang
Adam C. ElNaggar
Ramesh Narayanan
Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer
Journal of Personalized Medicine
integrin-linked kinase (ILK)
ovarian cancer
sgRNA
gene expression
microarray
xenograft
author_facet Michael A. Ulm
Tiffany M. Redfern
Ben R. Wilson
Suriyan Ponnusamy
Sarah Asemota
Patrick W. Blackburn
Yinan Wang
Adam C. ElNaggar
Ramesh Narayanan
author_sort Michael A. Ulm
title Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer
title_short Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer
title_full Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer
title_fullStr Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer
title_full_unstemmed Integrin-Linked Kinase Is a Novel Therapeutic Target in Ovarian Cancer
title_sort integrin-linked kinase is a novel therapeutic target in ovarian cancer
publisher MDPI AG
series Journal of Personalized Medicine
issn 2075-4426
publishDate 2020-11-01
description Objective: The objective of this study is to identify and validate novel therapeutic target(s) in ovarian cancer. Background: Development of targeted therapeutics in ovarian cancer has been limited by molecular heterogeneity. Although gene expression datasets are available, most of them lack appropriate pair-matched controls to define the alterations that result in the transformation of normal ovarian cells to cancerous cells. Methods: We used microarray to compare the gene expression of treatment-naïve ovarian cancer tissue samples to pair-matched normal adjacent ovarian tissue from 24 patients. Ingenuity Pathway Analysis (IPA) was used to identify target pathways for further analysis. Integrin-linked kinase (ILK) expression in SKOV3 and OV90 cells was determined using Western blot. ILK was knocked down using CRISPR/Cas9 constructs. Subcutaneous xenograft study to determine the effect of ILK knockdown on tumor growth was performed in NOD SCID gamma mice. Results: Significant upregulation of the ILK pathway was identified in 22 of the 24 cancer specimens, identifying it as a potential player that could contribute to the transformation of normal ovarian cells to cancerous cells. Knockdown of ILK in SKOV3 cells resulted in decreased cell proliferation and tumor growth, and inhibition of downstream kinase, AKT (protein kinase B). These results were further validated using an ILK-1 chemical inhibitor, compound 22. Conclusion: Our initial findings validate ILK as a potential therapeutic target for molecular inhibition in ovarian cancer, which warrants further investigation.
topic integrin-linked kinase (ILK)
ovarian cancer
sgRNA
gene expression
microarray
xenograft
url https://www.mdpi.com/2075-4426/10/4/246
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