Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma

Abstract Multiple myeloma (MM) is an aggressive plasma cell neoplasm characterized by genomic heterogeneity. Superenhancers (SEs) are defined as large clusters of enhancers in close genomic proximity, which regulate genes for maintaining cellular identity and promote oncogenic transcription to which...

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Main Authors: Yunlu Jia, Jianbiao Zhou, Tze King Tan, Tae-Hoon Chung, Regina Wan Ju Wong, Jing-Yuan Chooi, Julia Sze Lynn Lim, Takaomi Sanda, Melissa Ooi, Sanjay De Mel, Cinnie Soekojo, Yongxia Chen, Enfan Zhang, Zhen Cai, Peng Shen, Jian Ruan, Wee-Joo Chng
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Blood Cancer Journal
Online Access:https://doi.org/10.1038/s41408-021-00421-7
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author Yunlu Jia
Jianbiao Zhou
Tze King Tan
Tae-Hoon Chung
Regina Wan Ju Wong
Jing-Yuan Chooi
Julia Sze Lynn Lim
Takaomi Sanda
Melissa Ooi
Sanjay De Mel
Cinnie Soekojo
Yongxia Chen
Enfan Zhang
Zhen Cai
Peng Shen
Jian Ruan
Wee-Joo Chng
spellingShingle Yunlu Jia
Jianbiao Zhou
Tze King Tan
Tae-Hoon Chung
Regina Wan Ju Wong
Jing-Yuan Chooi
Julia Sze Lynn Lim
Takaomi Sanda
Melissa Ooi
Sanjay De Mel
Cinnie Soekojo
Yongxia Chen
Enfan Zhang
Zhen Cai
Peng Shen
Jian Ruan
Wee-Joo Chng
Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
Blood Cancer Journal
author_facet Yunlu Jia
Jianbiao Zhou
Tze King Tan
Tae-Hoon Chung
Regina Wan Ju Wong
Jing-Yuan Chooi
Julia Sze Lynn Lim
Takaomi Sanda
Melissa Ooi
Sanjay De Mel
Cinnie Soekojo
Yongxia Chen
Enfan Zhang
Zhen Cai
Peng Shen
Jian Ruan
Wee-Joo Chng
author_sort Yunlu Jia
title Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
title_short Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
title_full Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
title_fullStr Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
title_full_unstemmed Myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
title_sort myeloma-specific superenhancers affect genes of biological and clinical relevance in myeloma
publisher Nature Publishing Group
series Blood Cancer Journal
issn 2044-5385
publishDate 2021-02-01
description Abstract Multiple myeloma (MM) is an aggressive plasma cell neoplasm characterized by genomic heterogeneity. Superenhancers (SEs) are defined as large clusters of enhancers in close genomic proximity, which regulate genes for maintaining cellular identity and promote oncogenic transcription to which cancer cells highly addicted. Here, we analyzed cis-regulatory elements in MM samples with H3K27ac ChIP-seq, to identify novel SE-associated genes involved in the myeloma pathogenesis. SEs and their associated genes in cancerous tissue were compared with the control samples, and we found SE analysis alone uncovered cell-lineage-specific transcription factors and well-known oncogenes ST3GAL6 and ADM. Using a transcriptional CDK7 inhibitor, THZ1, coupled with H3K27ac ChlP-seq, we identified MAGI2 as a novel SE-associated gene of myeloma cells. Elevated MAGI2 was related to myelomagenesis with gradual increased expression from MGUS, SMM to newly diagnosed and relapsed MM. High prevalence of MAGI2 was also associated with poor survival of MM patients. Importantly, inhibition of the SE activity associated with MAGI2 decreased MAGI2 expression, inhibited cell growth and induced cell apoptosis. Mechanistically, we revealed that the oncogenic transcription factor, MAF, directly bound to the SE region and activated gene transcription. In summary, the discoveries of these acquired SEs-associated genes and the novel mechanism by which they are regulated provide new insights into MM biology and MAGI2-MAF-SE regulatory circuit offer potential novel targets for disease treatment.
url https://doi.org/10.1038/s41408-021-00421-7
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spelling doaj-84a9518ee10c44cc91668e7428907d282021-02-14T12:11:00ZengNature Publishing GroupBlood Cancer Journal2044-53852021-02-0111211310.1038/s41408-021-00421-7Myeloma-specific superenhancers affect genes of biological and clinical relevance in myelomaYunlu Jia0Jianbiao Zhou1Tze King Tan2Tae-Hoon Chung3Regina Wan Ju Wong4Jing-Yuan Chooi5Julia Sze Lynn Lim6Takaomi Sanda7Melissa Ooi8Sanjay De Mel9Cinnie Soekojo10Yongxia Chen11Enfan Zhang12Zhen Cai13Peng Shen14Jian Ruan15Wee-Joo Chng16Cancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineDepartment of Hematology-Oncology, National University Cancer Institute of Singapore (NCIS), The National University Health System (NUHS)Department of Hematology-Oncology, National University Cancer Institute of Singapore (NCIS), The National University Health System (NUHS)Department of Hematology-Oncology, National University Cancer Institute of Singapore (NCIS), The National University Health System (NUHS)Department of Surgical Oncology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang UniversityBone Marrow Transplantation Center, the First Affiliated Hospital, Zhejiang University School of MedicineBone Marrow Transplantation Center, the First Affiliated Hospital, Zhejiang University School of MedicineDepartment of Medical oncology, the First Affiliated Hospital, Zhejiang University School of MedicineDepartment of Medical oncology, the First Affiliated Hospital, Zhejiang University School of MedicineCancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, Centre for Translational MedicineAbstract Multiple myeloma (MM) is an aggressive plasma cell neoplasm characterized by genomic heterogeneity. Superenhancers (SEs) are defined as large clusters of enhancers in close genomic proximity, which regulate genes for maintaining cellular identity and promote oncogenic transcription to which cancer cells highly addicted. Here, we analyzed cis-regulatory elements in MM samples with H3K27ac ChIP-seq, to identify novel SE-associated genes involved in the myeloma pathogenesis. SEs and their associated genes in cancerous tissue were compared with the control samples, and we found SE analysis alone uncovered cell-lineage-specific transcription factors and well-known oncogenes ST3GAL6 and ADM. Using a transcriptional CDK7 inhibitor, THZ1, coupled with H3K27ac ChlP-seq, we identified MAGI2 as a novel SE-associated gene of myeloma cells. Elevated MAGI2 was related to myelomagenesis with gradual increased expression from MGUS, SMM to newly diagnosed and relapsed MM. High prevalence of MAGI2 was also associated with poor survival of MM patients. Importantly, inhibition of the SE activity associated with MAGI2 decreased MAGI2 expression, inhibited cell growth and induced cell apoptosis. Mechanistically, we revealed that the oncogenic transcription factor, MAF, directly bound to the SE region and activated gene transcription. In summary, the discoveries of these acquired SEs-associated genes and the novel mechanism by which they are regulated provide new insights into MM biology and MAGI2-MAF-SE regulatory circuit offer potential novel targets for disease treatment.https://doi.org/10.1038/s41408-021-00421-7