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CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma

BACKGROUND: Ewing sarcoma (ES) is an aggressive childhood bone and soft tissue cancer. KIAA1429 is one type of N6-methyladenosine (m6A) writer that plays a tumor-progressive role in various cancers, but the role of KIAA1429 in ES remains to be elucidated. The aim of the study was to investigate the...

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Autores principales: Tan, Kezhe, Lu, Wenjie, Chen, Feng, Shi, Hao, Ma, Yingxuan, Chen, Zhou, Wu, Wei, Lv, Zhibao, Mo, Jialin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537923/
https://www.ncbi.nlm.nih.gov/pubmed/37759224
http://dx.doi.org/10.1186/s13046-023-02828-5
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author Tan, Kezhe
Lu, Wenjie
Chen, Feng
Shi, Hao
Ma, Yingxuan
Chen, Zhou
Wu, Wei
Lv, Zhibao
Mo, Jialin
author_facet Tan, Kezhe
Lu, Wenjie
Chen, Feng
Shi, Hao
Ma, Yingxuan
Chen, Zhou
Wu, Wei
Lv, Zhibao
Mo, Jialin
author_sort Tan, Kezhe
collection PubMed
description BACKGROUND: Ewing sarcoma (ES) is an aggressive childhood bone and soft tissue cancer. KIAA1429 is one type of N6-methyladenosine (m6A) writer that plays a tumor-progressive role in various cancers, but the role of KIAA1429 in ES remains to be elucidated. The aim of the study was to investigate the role of KIAA1429 in ES. METHODS: We performed a multi-omic screen including CRISPR-Cas9 functional genomic and transcriptomic approaches, and identified that KIAA1429 played a significant role in ES progression. Gene knockdown, quantitative real-time PCR (Q-RT-PCR), immunoblotting, CellTiter-Glo assays, clonogenic assays, a subcutaneous xenograft model and immunohistochemistry were used to assess the functional role of KIAA1429 in ES. We mainly conducted RNA sequencing (RNA-seq) in ES cells to analyze the downstream regulatory mechanism of KIAA1429. An integrative analysis of chromatin immunoprecipitation sequencing (ChIP-seq) and RNA-seq indicated the upstream regulatory mechanism of KIAA1429. RESULTS: In vitro and in vivo CRISPR-Cas9 knockout screening identified KIAA1429 as an ES-dependent gene. Genetic suppression of KIAA1429 inhibited ES cell proliferation and tumorigenicity both in vitro and in vivo. Further studies revealed that KIAA1429 promotes ES tumorigenesis by regulating the ribosome-associated cell cycle and cancer-related inflammation. Interestingly, we found that STAT3 was a target of KIAA1429 and that a STAT3 inhibitor reduced KIAA1429 transcript levels, indicating positive feedback between KIAA1429 and STAT3. Finally, we found that NKX2-2 bound to the KIAA1429 promoter and transactivated KIAA1429. CONCLUSION: Our study systematically analyzed ES-dependent epigenetic/transcriptional regulatory genes and identified KIAA1429 as a biomarker of tumor progression in ES, providing a potential therapeutic target for treating ES. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-023-02828-5.
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spelling pubmed-105379232023-09-29 CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma Tan, Kezhe Lu, Wenjie Chen, Feng Shi, Hao Ma, Yingxuan Chen, Zhou Wu, Wei Lv, Zhibao Mo, Jialin J Exp Clin Cancer Res Research BACKGROUND: Ewing sarcoma (ES) is an aggressive childhood bone and soft tissue cancer. KIAA1429 is one type of N6-methyladenosine (m6A) writer that plays a tumor-progressive role in various cancers, but the role of KIAA1429 in ES remains to be elucidated. The aim of the study was to investigate the role of KIAA1429 in ES. METHODS: We performed a multi-omic screen including CRISPR-Cas9 functional genomic and transcriptomic approaches, and identified that KIAA1429 played a significant role in ES progression. Gene knockdown, quantitative real-time PCR (Q-RT-PCR), immunoblotting, CellTiter-Glo assays, clonogenic assays, a subcutaneous xenograft model and immunohistochemistry were used to assess the functional role of KIAA1429 in ES. We mainly conducted RNA sequencing (RNA-seq) in ES cells to analyze the downstream regulatory mechanism of KIAA1429. An integrative analysis of chromatin immunoprecipitation sequencing (ChIP-seq) and RNA-seq indicated the upstream regulatory mechanism of KIAA1429. RESULTS: In vitro and in vivo CRISPR-Cas9 knockout screening identified KIAA1429 as an ES-dependent gene. Genetic suppression of KIAA1429 inhibited ES cell proliferation and tumorigenicity both in vitro and in vivo. Further studies revealed that KIAA1429 promotes ES tumorigenesis by regulating the ribosome-associated cell cycle and cancer-related inflammation. Interestingly, we found that STAT3 was a target of KIAA1429 and that a STAT3 inhibitor reduced KIAA1429 transcript levels, indicating positive feedback between KIAA1429 and STAT3. Finally, we found that NKX2-2 bound to the KIAA1429 promoter and transactivated KIAA1429. CONCLUSION: Our study systematically analyzed ES-dependent epigenetic/transcriptional regulatory genes and identified KIAA1429 as a biomarker of tumor progression in ES, providing a potential therapeutic target for treating ES. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-023-02828-5. BioMed Central 2023-09-28 /pmc/articles/PMC10537923/ /pubmed/37759224 http://dx.doi.org/10.1186/s13046-023-02828-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Tan, Kezhe
Lu, Wenjie
Chen, Feng
Shi, Hao
Ma, Yingxuan
Chen, Zhou
Wu, Wei
Lv, Zhibao
Mo, Jialin
CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
title CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
title_full CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
title_fullStr CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
title_full_unstemmed CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
title_short CRISPR-Cas9 knockout screening identifies KIAA1429 as an essential gene in Ewing sarcoma
title_sort crispr-cas9 knockout screening identifies kiaa1429 as an essential gene in ewing sarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537923/
https://www.ncbi.nlm.nih.gov/pubmed/37759224
http://dx.doi.org/10.1186/s13046-023-02828-5
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