Unintended target effect of anti-BCL-2 DNAi

Abdul Shukkur Ebrahim,1 Mustapha Kandouz,2 Nada Emara,1 Amara B Sugalski,3 Leonard Lipovich,3 Ayad M Al-Katib1 1Lymphoma Research Laboratory, 2Department of Pathology, School of Medicine, 3Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, USA Introduction: Previous res...

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Main Authors: Ebrahim AS, Kandouz M, Emara N, Sugalski AB, Lipovich L, Al-Katib AM
Format: Article
Language:English
Published: Dove Medical Press 2017-09-01
Series:Cancer Management and Research
Subjects:
Online Access:https://www.dovepress.com/unintended-target-effect-of-anti-bcl-2-dnai-peer-reviewed-article-CMAR
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spelling doaj-de1c9e7e512d4f5b8bc76bb2cc0ecfed2020-11-24T21:06:06ZengDove Medical PressCancer Management and Research1179-13222017-09-01Volume 942743234842Unintended target effect of anti-BCL-2 DNAiEbrahim ASKandouz MEmara NSugalski ABLipovich LAl-Katib AMAbdul Shukkur Ebrahim,1 Mustapha Kandouz,2 Nada Emara,1 Amara B Sugalski,3 Leonard Lipovich,3 Ayad M Al-Katib1 1Lymphoma Research Laboratory, 2Department of Pathology, School of Medicine, 3Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, USA Introduction: Previous research suggested that a novel compound PNT2258 inhibits B-cell lymphoma 2 (BCL-2) transcription by DNA interference (DNAi) and demonstrated its activity in preclinical xenograft models and in a pilot Phase II clinical trial in non-Hodgkin’s lymphoma (NHL). While the drug downregulates BCL-2 at the promoter, mRNA, and protein levels, there is a significant homology (13–16 bases) between PNT100 and a number of promoters of genes involved in cell cycle regulation and survival. In this study, we identify cyclin-dependent kinase-4 (CDK4) as an unintended target gene of PNT2258 and examine its relevance to NHL.Methods: We performed a Basic Local Alignment Search Tool (BLAST) homology search using PNT100 DNAi sequences. Also, we conducted CDK4 promoter assay in K562 cells and studied the protein expression of CDK4 in Wayne State University (WSU)-follicular small cleaved cell lymphoma (FSCCL), WSU-diffuse large cell lymphoma, and WSU-Waldenström’s macroglobulinemia (WM) lymphoma cells.Results: BLAST homology search showed that PNT100 completely binds to BCL-2 gene as expected. However, there was 100% homology in a stretch of 14 bases (8–21) between PNT100 and CDK4. PNT2258 strongly inhibited CDK4 promoter activity in K562 cells. Moreover, CDK4 protein expression was significantly downregulated by PNT2258 in WSU-FSCCL and WSU-WM cell lines. Discussion: DNAi may work not only through knocking down the intended gene but also by knocking down other genes. PNT2258 affects CDK4 expression and promoter activity. Results of the present study suggest a broader mechanism of action for DNAi targeting both intended (BCL-2) and unintended (CDK4) genes. Keywords: non-Hodgkin’s lymphoma, BCL-2, PNT2258, BLAST, CDK4https://www.dovepress.com/unintended-target-effect-of-anti-bcl-2-dnai-peer-reviewed-article-CMARnon-Hodgkin's lymphomaDNAiPNT2258BLASTCDK4
collection DOAJ
language English
format Article
sources DOAJ
author Ebrahim AS
Kandouz M
Emara N
Sugalski AB
Lipovich L
Al-Katib AM
spellingShingle Ebrahim AS
Kandouz M
Emara N
Sugalski AB
Lipovich L
Al-Katib AM
Unintended target effect of anti-BCL-2 DNAi
Cancer Management and Research
non-Hodgkin's lymphoma
DNAi
PNT2258
BLAST
CDK4
author_facet Ebrahim AS
Kandouz M
Emara N
Sugalski AB
Lipovich L
Al-Katib AM
author_sort Ebrahim AS
title Unintended target effect of anti-BCL-2 DNAi
title_short Unintended target effect of anti-BCL-2 DNAi
title_full Unintended target effect of anti-BCL-2 DNAi
title_fullStr Unintended target effect of anti-BCL-2 DNAi
title_full_unstemmed Unintended target effect of anti-BCL-2 DNAi
title_sort unintended target effect of anti-bcl-2 dnai
publisher Dove Medical Press
series Cancer Management and Research
issn 1179-1322
publishDate 2017-09-01
description Abdul Shukkur Ebrahim,1 Mustapha Kandouz,2 Nada Emara,1 Amara B Sugalski,3 Leonard Lipovich,3 Ayad M Al-Katib1 1Lymphoma Research Laboratory, 2Department of Pathology, School of Medicine, 3Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, USA Introduction: Previous research suggested that a novel compound PNT2258 inhibits B-cell lymphoma 2 (BCL-2) transcription by DNA interference (DNAi) and demonstrated its activity in preclinical xenograft models and in a pilot Phase II clinical trial in non-Hodgkin’s lymphoma (NHL). While the drug downregulates BCL-2 at the promoter, mRNA, and protein levels, there is a significant homology (13–16 bases) between PNT100 and a number of promoters of genes involved in cell cycle regulation and survival. In this study, we identify cyclin-dependent kinase-4 (CDK4) as an unintended target gene of PNT2258 and examine its relevance to NHL.Methods: We performed a Basic Local Alignment Search Tool (BLAST) homology search using PNT100 DNAi sequences. Also, we conducted CDK4 promoter assay in K562 cells and studied the protein expression of CDK4 in Wayne State University (WSU)-follicular small cleaved cell lymphoma (FSCCL), WSU-diffuse large cell lymphoma, and WSU-Waldenström’s macroglobulinemia (WM) lymphoma cells.Results: BLAST homology search showed that PNT100 completely binds to BCL-2 gene as expected. However, there was 100% homology in a stretch of 14 bases (8–21) between PNT100 and CDK4. PNT2258 strongly inhibited CDK4 promoter activity in K562 cells. Moreover, CDK4 protein expression was significantly downregulated by PNT2258 in WSU-FSCCL and WSU-WM cell lines. Discussion: DNAi may work not only through knocking down the intended gene but also by knocking down other genes. PNT2258 affects CDK4 expression and promoter activity. Results of the present study suggest a broader mechanism of action for DNAi targeting both intended (BCL-2) and unintended (CDK4) genes. Keywords: non-Hodgkin’s lymphoma, BCL-2, PNT2258, BLAST, CDK4
topic non-Hodgkin's lymphoma
DNAi
PNT2258
BLAST
CDK4
url https://www.dovepress.com/unintended-target-effect-of-anti-bcl-2-dnai-peer-reviewed-article-CMAR
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