Biological Insights into Chemotherapy Resistance in Ovarian Cancer

The majority of patients with high-grade serous ovarian cancer (HGSOC) initially respond to chemotherapy; however, most will develop chemotherapy resistance. Gene signatures may change with the development of chemotherapy resistance in this population, which is important as it may lead to tailored t...

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Main Authors: Michelle A. Glasgow, Peter Argenta, Juan E. Abrahante, Mihir Shetty, Shobhana Talukdar, Paula A. Croonquist, Mahmoud A. Khalifa, Timothy K. Starr
Format: Article
Language:English
Published: MDPI AG 2019-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/9/2131
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spelling doaj-5d3deef6ec424645b88890fb7176e5762020-11-25T01:33:55ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-04-01209213110.3390/ijms20092131ijms20092131Biological Insights into Chemotherapy Resistance in Ovarian CancerMichelle A. Glasgow0Peter Argenta1Juan E. Abrahante2Mihir Shetty3Shobhana Talukdar4Paula A. Croonquist5Mahmoud A. Khalifa6Timothy K. Starr7Department of Obstetrics, Gynecology & Women’s Health, University of Minnesota, Minneapolis, MN 55455, USADepartment of Obstetrics, Gynecology & Women’s Health, University of Minnesota, Minneapolis, MN 55455, USAMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USADepartment of Obstetrics, Gynecology & Women’s Health, University of Minnesota, Minneapolis, MN 55455, USADepartment of Obstetrics, Gynecology & Women’s Health, University of Minnesota, Minneapolis, MN 55455, USADepartment of Biology, Anoka Ramsey Community College, Coon Rapids, MN 55455, USADepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USADepartment of Obstetrics, Gynecology & Women’s Health, University of Minnesota, Minneapolis, MN 55455, USAThe majority of patients with high-grade serous ovarian cancer (HGSOC) initially respond to chemotherapy; however, most will develop chemotherapy resistance. Gene signatures may change with the development of chemotherapy resistance in this population, which is important as it may lead to tailored therapies. The objective of this study was to compare tumor gene expression profiles in patients before and after treatment with neoadjuvant chemotherapy (NACT). Tumor samples were collected from six patients diagnosed with HGSOC before and after administration of NACT. RNA extraction and whole transcriptome sequencing was performed. Differential gene expression, hierarchical clustering, gene set enrichment analysis, and pathway analysis were examined in all of the samples. Tumor samples clustered based on exposure to chemotherapy as opposed to patient source. Pre-NACT samples were enriched for multiple pathways involving cell cycle growth. Post-NACT samples were enriched for drug transport and peroxisome pathways. Molecular subtypes based on the pre-NACT sample (differentiated, mesenchymal, proliferative and immunoreactive) changed in four patients after administration of NACT. Multiple changes in tumor gene expression profiles after exposure to NACT were identified from this pilot study and warrant further attention as they may indicate early changes in the development of chemotherapy resistance.https://www.mdpi.com/1422-0067/20/9/2131ovarian cancerchemotherapy resistancegene expression
collection DOAJ
language English
format Article
sources DOAJ
author Michelle A. Glasgow
Peter Argenta
Juan E. Abrahante
Mihir Shetty
Shobhana Talukdar
Paula A. Croonquist
Mahmoud A. Khalifa
Timothy K. Starr
spellingShingle Michelle A. Glasgow
Peter Argenta
Juan E. Abrahante
Mihir Shetty
Shobhana Talukdar
Paula A. Croonquist
Mahmoud A. Khalifa
Timothy K. Starr
Biological Insights into Chemotherapy Resistance in Ovarian Cancer
International Journal of Molecular Sciences
ovarian cancer
chemotherapy resistance
gene expression
author_facet Michelle A. Glasgow
Peter Argenta
Juan E. Abrahante
Mihir Shetty
Shobhana Talukdar
Paula A. Croonquist
Mahmoud A. Khalifa
Timothy K. Starr
author_sort Michelle A. Glasgow
title Biological Insights into Chemotherapy Resistance in Ovarian Cancer
title_short Biological Insights into Chemotherapy Resistance in Ovarian Cancer
title_full Biological Insights into Chemotherapy Resistance in Ovarian Cancer
title_fullStr Biological Insights into Chemotherapy Resistance in Ovarian Cancer
title_full_unstemmed Biological Insights into Chemotherapy Resistance in Ovarian Cancer
title_sort biological insights into chemotherapy resistance in ovarian cancer
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-04-01
description The majority of patients with high-grade serous ovarian cancer (HGSOC) initially respond to chemotherapy; however, most will develop chemotherapy resistance. Gene signatures may change with the development of chemotherapy resistance in this population, which is important as it may lead to tailored therapies. The objective of this study was to compare tumor gene expression profiles in patients before and after treatment with neoadjuvant chemotherapy (NACT). Tumor samples were collected from six patients diagnosed with HGSOC before and after administration of NACT. RNA extraction and whole transcriptome sequencing was performed. Differential gene expression, hierarchical clustering, gene set enrichment analysis, and pathway analysis were examined in all of the samples. Tumor samples clustered based on exposure to chemotherapy as opposed to patient source. Pre-NACT samples were enriched for multiple pathways involving cell cycle growth. Post-NACT samples were enriched for drug transport and peroxisome pathways. Molecular subtypes based on the pre-NACT sample (differentiated, mesenchymal, proliferative and immunoreactive) changed in four patients after administration of NACT. Multiple changes in tumor gene expression profiles after exposure to NACT were identified from this pilot study and warrant further attention as they may indicate early changes in the development of chemotherapy resistance.
topic ovarian cancer
chemotherapy resistance
gene expression
url https://www.mdpi.com/1422-0067/20/9/2131
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