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Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma

BACKGROUND: Esophageal squamous cell carcinoma (ESCC) is one of the most lethal malignancies with poor prognosis. Cancer-testis genes (CTGs) have been vigorously pursued as targets for cancer immunotherapy, but the expressive patterns and functional roles of CTGs remain unclear in ESCC. METHODS: A s...

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Autores principales: Xu, Jing, Zhu, Chengxiang, Yu, Yue, Wu, Weibing, Cao, Jing, Li, Zhihua, Dai, Juncheng, Wang, Cheng, Tang, Yu, Zhu, Quan, Wang, Jun, Wen, Wei, Xue, Lei, Zhen, Fuxi, Liu, Jinyuan, Huang, Chenjun, Zhao, Fei, Zhou, Yue, He, Zhicheng, Pan, Xianglong, Wei, Haixing, Zhu, Yining, He, Yaozhou, Que, Jun, Luo, Jinghua, Chen, Liang, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710982/
https://www.ncbi.nlm.nih.gov/pubmed/31324603
http://dx.doi.org/10.1016/j.ebiom.2019.07.030
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author Xu, Jing
Zhu, Chengxiang
Yu, Yue
Wu, Weibing
Cao, Jing
Li, Zhihua
Dai, Juncheng
Wang, Cheng
Tang, Yu
Zhu, Quan
Wang, Jun
Wen, Wei
Xue, Lei
Zhen, Fuxi
Liu, Jinyuan
Huang, Chenjun
Zhao, Fei
Zhou, Yue
He, Zhicheng
Pan, Xianglong
Wei, Haixing
Zhu, Yining
He, Yaozhou
Que, Jun
Luo, Jinghua
Chen, Liang
Wang, Wei
author_facet Xu, Jing
Zhu, Chengxiang
Yu, Yue
Wu, Weibing
Cao, Jing
Li, Zhihua
Dai, Juncheng
Wang, Cheng
Tang, Yu
Zhu, Quan
Wang, Jun
Wen, Wei
Xue, Lei
Zhen, Fuxi
Liu, Jinyuan
Huang, Chenjun
Zhao, Fei
Zhou, Yue
He, Zhicheng
Pan, Xianglong
Wei, Haixing
Zhu, Yining
He, Yaozhou
Que, Jun
Luo, Jinghua
Chen, Liang
Wang, Wei
author_sort Xu, Jing
collection PubMed
description BACKGROUND: Esophageal squamous cell carcinoma (ESCC) is one of the most lethal malignancies with poor prognosis. Cancer-testis genes (CTGs) have been vigorously pursued as targets for cancer immunotherapy, but the expressive patterns and functional roles of CTGs remain unclear in ESCC. METHODS: A systematic screening strategy was adopted to screen CTGs in ESCC by integrating multiple public databases and RNA expression microarray data from 119 ESCC subjects. For the newly identified ESCC prognosis-associated CTGs, an independent cohort of 118 patients with ESCC was recruited to validate the relationship via immunohistochemistry. Furthermore, functional assays were performed to determine the underlying mechanisms. FINDINGS: 21 genes were recognized as CTGs, in particular, CDCA5 was aberrantly upregulated in ESCC tissues and significantly associated with poor prognosis (HR = 1.85, 95%CI: 1.14–3.01, P = .013). Immunohistochemical staining confirmed that positive CDCA5 expression was associated with advanced TNM staging and a shorter overall survival rate (45.59% vs 28.00% for CDCA5−/+ subjects, P = 1.86 × 10(−3)). H3K27 acetylation in CDCA5 promoter might lead to the activation of CDCA5 during ESCC tumorigenesis. Functionally, in vitro assay of gain- and loss-of-function of CDCA5 suggested that CDCA5 could promote ESCC cells proliferation, invasion, migration, apoptosis resistance and reduce chemosensitivity to cisplatin. Moreover, in vivo assay showed that silenced CDCA5 could inhibit tumor growth. Mechanistically, CDCA5 knockdown led to an arrest in G2/M phase and changes in the expression of factors that played fundamental roles in the cell cycle pathway. INTERPRETATION: CDCA5 contributed to ESCC progression and might serve as an attractive target for ESCC immunotherapy. FUND: This work was supported by the Natural Science Foundation of Jiangsu Province (No. BK20181083 and BK20181496), Jiangsu Top Expert Program in Six Professions (No. WSW-003 and WSW-007), Major Program of Science and Technology Foundation of Jiangsu Province (No. BE2016790 and BE2018746), Jiangsu Medical Young Talent Project (No. QNRC2016566), the Program of Jiangsu Medical Innovation Team (No. CXTDA2017006), Postgraduate Research & Practice Innovation Program of Jiangsu Province (KYCX18_1487) and Jiangsu Province 333 Talents Project (No. BRA2017545).
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spelling pubmed-67109822019-08-29 Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma Xu, Jing Zhu, Chengxiang Yu, Yue Wu, Weibing Cao, Jing Li, Zhihua Dai, Juncheng Wang, Cheng Tang, Yu Zhu, Quan Wang, Jun Wen, Wei Xue, Lei Zhen, Fuxi Liu, Jinyuan Huang, Chenjun Zhao, Fei Zhou, Yue He, Zhicheng Pan, Xianglong Wei, Haixing Zhu, Yining He, Yaozhou Que, Jun Luo, Jinghua Chen, Liang Wang, Wei EBioMedicine Research paper BACKGROUND: Esophageal squamous cell carcinoma (ESCC) is one of the most lethal malignancies with poor prognosis. Cancer-testis genes (CTGs) have been vigorously pursued as targets for cancer immunotherapy, but the expressive patterns and functional roles of CTGs remain unclear in ESCC. METHODS: A systematic screening strategy was adopted to screen CTGs in ESCC by integrating multiple public databases and RNA expression microarray data from 119 ESCC subjects. For the newly identified ESCC prognosis-associated CTGs, an independent cohort of 118 patients with ESCC was recruited to validate the relationship via immunohistochemistry. Furthermore, functional assays were performed to determine the underlying mechanisms. FINDINGS: 21 genes were recognized as CTGs, in particular, CDCA5 was aberrantly upregulated in ESCC tissues and significantly associated with poor prognosis (HR = 1.85, 95%CI: 1.14–3.01, P = .013). Immunohistochemical staining confirmed that positive CDCA5 expression was associated with advanced TNM staging and a shorter overall survival rate (45.59% vs 28.00% for CDCA5−/+ subjects, P = 1.86 × 10(−3)). H3K27 acetylation in CDCA5 promoter might lead to the activation of CDCA5 during ESCC tumorigenesis. Functionally, in vitro assay of gain- and loss-of-function of CDCA5 suggested that CDCA5 could promote ESCC cells proliferation, invasion, migration, apoptosis resistance and reduce chemosensitivity to cisplatin. Moreover, in vivo assay showed that silenced CDCA5 could inhibit tumor growth. Mechanistically, CDCA5 knockdown led to an arrest in G2/M phase and changes in the expression of factors that played fundamental roles in the cell cycle pathway. INTERPRETATION: CDCA5 contributed to ESCC progression and might serve as an attractive target for ESCC immunotherapy. FUND: This work was supported by the Natural Science Foundation of Jiangsu Province (No. BK20181083 and BK20181496), Jiangsu Top Expert Program in Six Professions (No. WSW-003 and WSW-007), Major Program of Science and Technology Foundation of Jiangsu Province (No. BE2016790 and BE2018746), Jiangsu Medical Young Talent Project (No. QNRC2016566), the Program of Jiangsu Medical Innovation Team (No. CXTDA2017006), Postgraduate Research & Practice Innovation Program of Jiangsu Province (KYCX18_1487) and Jiangsu Province 333 Talents Project (No. BRA2017545). Elsevier 2019-07-16 /pmc/articles/PMC6710982/ /pubmed/31324603 http://dx.doi.org/10.1016/j.ebiom.2019.07.030 Text en © 2019 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Xu, Jing
Zhu, Chengxiang
Yu, Yue
Wu, Weibing
Cao, Jing
Li, Zhihua
Dai, Juncheng
Wang, Cheng
Tang, Yu
Zhu, Quan
Wang, Jun
Wen, Wei
Xue, Lei
Zhen, Fuxi
Liu, Jinyuan
Huang, Chenjun
Zhao, Fei
Zhou, Yue
He, Zhicheng
Pan, Xianglong
Wei, Haixing
Zhu, Yining
He, Yaozhou
Que, Jun
Luo, Jinghua
Chen, Liang
Wang, Wei
Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma
title Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma
title_full Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma
title_fullStr Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma
title_full_unstemmed Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma
title_short Systematic cancer-testis gene expression analysis identified CDCA5 as a potential therapeutic target in esophageal squamous cell carcinoma
title_sort systematic cancer-testis gene expression analysis identified cdca5 as a potential therapeutic target in esophageal squamous cell carcinoma
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710982/
https://www.ncbi.nlm.nih.gov/pubmed/31324603
http://dx.doi.org/10.1016/j.ebiom.2019.07.030
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