Evidence map›Paper›PMID 40504421›Full record

ArticleDiscover oncology2025

Histone demethylase JMJD2D emerges as a novel prognostic biomarker and exhibits correlation with immune infiltration in lung adenocarcinoma.

Bona Liu, Hui Hao, Zhen Wang, Yingchun Li, Cheng Du, Jian Ming, Shuang Zhang, Lin Zhou, Dazhi Liu

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Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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9 authors.

Bona Liu *Department of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Hui Hao *Department of Medical Oncology, Hebei Cangzhou People's Hospital, Cangzhou, China.
Zhen Wang *Department of Oncology, General Hospital of Northern Theater Command, Dalian Medical University, Shenyang, China.
Yingchun LiDepartment of Pathology, General Hospital of Northern Theater Command, Shenyang, China.
Cheng DuDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, China.
Jian MingDepartment of Military Patient Management, General Hospital of Northern Theater Command, Shenyang, China.
Shuang ZhangDepartment of Military Patient Management, General Hospital of Northern Theater Command, Shenyang, China. jiejie65165@163.com.
Lin ZhouDepartment of Thoracic Surgery, Yuebei People's Hospital Affiliated to Shantou University Medical College, Shaoguan, China. zhoulin2002003@126.com.
Dazhi LiuDepartment of Thoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China. liudazhi_0526@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLysine demethylase 4D (KDM4D or JMJD2D) plays a significant role in tumorigenesis, development, and poor clinical outcomes. However, its roles in lung adenocarcinoma (LUAD) remains unclear. This study aimed to identify the role and molecular mechanisms of JMJD2D in LUAD.

methodsThe study investigated the correlation of JMJD2D with tumor development, immune cell infiltration, response to antitumor therapy, tumor mutation burden and prognostic values.

resultsJMJD2D had high expression in LUAD. High-JMJD2D expression was associated with poor survival outcomes and the T stage of LUAD patients. Furthermore, high-JMJD2D expression was linked to the decreased immune-related processes, associated with the increased Tregs and CD40 expression. Additionally, high-JMJD2D expression was associated with frequent alterations with higher TMB and resistance to BMS.708,163, Roscovitine, and Pyrimethamine, but sensitivities to ATRA, Bosutinib, and JNK. Inhibitor. VIII. Moreover, the study identified eight JMJD2D-related genes as a prognostic signature and constructed a predictive nomogram based on independent prognostic factors.

conclusionJMJD2D acts as an oncogene in LUAD and is involved in tumorigenesis, development, and poor clinical outcomes. Therefore, JMJD2D may serve as a potential prognostic biomarker in diagnosis and treatment of LUAD. The study emphasizes the importance of the molecular mechanisms of JMJD2D in LUAD.

Indexed as

Immune cell infiltrationJMJD2DLung adenocarcinoma (LUAD)Overall survivalTumor mutation burden (TMB)

Identifiers

PMID40504421
PMCPMC12162437

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