Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib

Human estrogen receptor positive cancer cells have mutations and make an excess of the HER2 protein and are far more aggressive than others cancers. Neratinib, an irreversible tyrosine kinase inhibitor is used to treat HER2 positive cancers. Neratinib targets HER2 and blocks its signal transduction...

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Main Authors: Sara Alkhezayem, Tanveer A. Wani, Salma Wakil, Ashwaq Aljuraysi, Seema Zargar
Format: Article
Language:English
Published: Elsevier 2020-08-01
Series:Saudi Pharmaceutical Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1319016420301365
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spelling doaj-a3fd516796aa499fa070253e79e8fb142020-11-25T03:15:24ZengElsevierSaudi Pharmaceutical Journal1319-01642020-08-01288963970Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinibSara Alkhezayem0Tanveer A. Wani1Salma Wakil2Ashwaq Aljuraysi3Seema Zargar4Department of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaDepartment of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Biochemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia; Corresponding author at: Department of Biochemistry, College of Science, King Saud University, Riyadh 11495, Saudi Arabia.Human estrogen receptor positive cancer cells have mutations and make an excess of the HER2 protein and are far more aggressive than others cancers. Neratinib, an irreversible tyrosine kinase inhibitor is used to treat HER2 positive cancers. Neratinib targets HER2 and blocks its signal transduction resulting in inhibition of cell proliferation and induction of apoptosis without any information about the molecular mechanism involved. To understand the underlying molecular mechanism transcriptome analysis was carried out in normal vs cancer induced SWR/J nude mice. Cancer was induced in SWR/J nude mice with intraperitoneal injection of 5 × 106 SKBR3 cells for 14 days. Histopathology confirmed the induction of cancer in liver and kidney after the tumor size was at least 0.5 cm. Genome wide Mouse U133 Array was used to analyze the effect of neratinib treatment on cancer. Validation of expression was done by qPCR and ELISA. Microscopic examination revealed that neratinib treatment has potential effects on cancerous liver. Transcriptome expression profiling showed 1481 transcripts differentially expressed by neratinib treatment. Transcriptome Analysis Console (TAC) showed that 532 upregulated transcripts were exclusively belonging to cell cycle, inflammation, olfaction, oxidative stress, HER, and EGFR1 while 949 downregulated transcripts were involved in immunology, drug resistance such as histocompatibility, T cell receptors, and immunoglobulins. The differentially expressed genes were considered significant under the criteria of an adjusted p-value < 0.02 and log2 ratios ≥ 1.0 and/or log2 ratios ≤  − 1.0 means two Fold change. qPCR assay and ELISA analysis was used to validate few genes involved in apoptosis and proliferation. This study provides new insights into the neratinib’s mode of action by cyclin-dependent kinase inhibitor-3 and calcium-activated chloride channel 3 as markers for treatment progress.http://www.sciencedirect.com/science/article/pii/S1319016420301365CancerExpression profilingMouse arrayNeratinibTranscriptome
collection DOAJ
language English
format Article
sources DOAJ
author Sara Alkhezayem
Tanveer A. Wani
Salma Wakil
Ashwaq Aljuraysi
Seema Zargar
spellingShingle Sara Alkhezayem
Tanveer A. Wani
Salma Wakil
Ashwaq Aljuraysi
Seema Zargar
Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
Saudi Pharmaceutical Journal
Cancer
Expression profiling
Mouse array
Neratinib
Transcriptome
author_facet Sara Alkhezayem
Tanveer A. Wani
Salma Wakil
Ashwaq Aljuraysi
Seema Zargar
author_sort Sara Alkhezayem
title Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
title_short Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
title_full Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
title_fullStr Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
title_full_unstemmed Transcriptome analysis of neratinib treated HER2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
title_sort transcriptome analysis of neratinib treated her2 positive cancer model vs untreated cancer unravels the molecular mechanism of action of neratinib
publisher Elsevier
series Saudi Pharmaceutical Journal
issn 1319-0164
publishDate 2020-08-01
description Human estrogen receptor positive cancer cells have mutations and make an excess of the HER2 protein and are far more aggressive than others cancers. Neratinib, an irreversible tyrosine kinase inhibitor is used to treat HER2 positive cancers. Neratinib targets HER2 and blocks its signal transduction resulting in inhibition of cell proliferation and induction of apoptosis without any information about the molecular mechanism involved. To understand the underlying molecular mechanism transcriptome analysis was carried out in normal vs cancer induced SWR/J nude mice. Cancer was induced in SWR/J nude mice with intraperitoneal injection of 5 × 106 SKBR3 cells for 14 days. Histopathology confirmed the induction of cancer in liver and kidney after the tumor size was at least 0.5 cm. Genome wide Mouse U133 Array was used to analyze the effect of neratinib treatment on cancer. Validation of expression was done by qPCR and ELISA. Microscopic examination revealed that neratinib treatment has potential effects on cancerous liver. Transcriptome expression profiling showed 1481 transcripts differentially expressed by neratinib treatment. Transcriptome Analysis Console (TAC) showed that 532 upregulated transcripts were exclusively belonging to cell cycle, inflammation, olfaction, oxidative stress, HER, and EGFR1 while 949 downregulated transcripts were involved in immunology, drug resistance such as histocompatibility, T cell receptors, and immunoglobulins. The differentially expressed genes were considered significant under the criteria of an adjusted p-value < 0.02 and log2 ratios ≥ 1.0 and/or log2 ratios ≤  − 1.0 means two Fold change. qPCR assay and ELISA analysis was used to validate few genes involved in apoptosis and proliferation. This study provides new insights into the neratinib’s mode of action by cyclin-dependent kinase inhibitor-3 and calcium-activated chloride channel 3 as markers for treatment progress.
topic Cancer
Expression profiling
Mouse array
Neratinib
Transcriptome
url http://www.sciencedirect.com/science/article/pii/S1319016420301365
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AT ashwaqaljuraysi transcriptomeanalysisofneratinibtreatedher2positivecancermodelvsuntreatedcancerunravelsthemolecularmechanismofactionofneratinib
AT seemazargar transcriptomeanalysisofneratinibtreatedher2positivecancermodelvsuntreatedcancerunravelsthemolecularmechanismofactionofneratinib
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