Evidence map›Paper›PMID 40591089›Full record

ArticleDiscover oncology2025

Pan-cancer analysis and validation of NT5DC2: emphasizing its prognostic significance and immunological role in TNBC.

Qing Luo, Xiandong Xie, Luyao Tian, Xiaomin Gao, Shu Li, Jinqiu Zhang, Limei Mo, Xue Zhu, Ke Wang, Yongxiang Yin

Abstract read
In one paragraph

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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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Qing Luo *Wuxi School of Medicine, Jiangnan University, Wuxi, 214122, Jiangsu, China.
Xiandong Xie *School of Clinical Medicine, Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China.
Luyao TianWuxi Maternity and Child Health Care Hospital, Affiliated Women's Hospital of Jiangnan University, Wuxi, 214002, Jiangsu, China.
Xiaomin GaoWuxi School of Medicine, Jiangnan University, Wuxi, 214122, Jiangsu, China.
Shu LiWuxi School of Medicine, Jiangnan University, Wuxi, 214122, Jiangsu, China.
Jinqiu ZhangWuxi Maternity and Child Health Care Hospital, Affiliated Women's Hospital of Jiangnan University, Wuxi, 214002, Jiangsu, China.
Limei MoSchool of Clinical Medicine, Youjiang Medical University for Nationalities, Baise, 533000, Guangxi, China.
Xue ZhuNHC Key Laboratory of Nuclear Medicine, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi, 214063, Jiangsu, China.
Ke WangNHC Key Laboratory of Nuclear Medicine, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi, 214063, Jiangsu, China. wangke@jsinm.org.
Yongxiang YinWuxi School of Medicine, Jiangnan University, Wuxi, 214122, Jiangsu, China. yinyrh@jiangnan.edu.cn.

Funding

Major Project of Wuxi Municipal Health Commission Z202303Project of Jiangsu Administration of Traditional Chinese Medicine MS2022145Project of Jiangsu Administration of Traditional Chinese Medicine MS2023166Project of Jiangsu Commission of Health H2023150
6 · The paper itself

Abstract

background5'-Nucleotidase Domain Containing 2 (NT5DC2), a member of the cNT5-II family that catalyzes nucleotide hydrolysis, plays a critical role in tumor initiation and progression. This study aims to elucidate the role of NT5DC2 across multiple cancers and to confirm its oncogenic significance in triple-negative breast cancer (TNBC).

methodsNT5DC2 expression patterns were analyzed across multiple databases to evaluate its diagnostic and prognostic value in various cancers. Immune correlation analyses were performed using ESTIMATE and CIBERSORT algorithms. KEGG pathway enrichment analysis was used to explore NT5DC2-associated molecular pathways. In TNBC, comprehensive bioinformatics approaches, including gene expression profiling, single-cell RNA sequencing, immune infiltration analysis, and gene set enrichment analysis (GSEA), were employed. Additionally, in vitro experiments were conducted to validate the oncogenic role of NT5DC2 in TNBC.

resultsHigh NT5DC2 expression was associated with poor prognosis and demonstrated significant clinical diagnostic value across several cancer types. In TNBC, NT5DC2 was found to be highly expressed and correlated with adverse outcomes. Single-cell RNA sequencing revealed that NT5DC2 is predominantly expressed in epithelial cells and may regulate immune cell behavior through the MIF signaling pathway. Enrichment and immune infiltration analyses further indicated that NT5DC2 is strongly associated with an immunosuppressive tumor microenvironment (TME). In vitro experiments showed that NT5DC2 knockdown significantly suppressed TNBC cell growth, whereas its overexpression exerted opposing effects, highlighting its therapeutic potential.

conclusionThis study identifies NT5DC2 as an oncogene with broad clinical relevance across multiple cancers. In TNBC, NT5DC2 contributes to an immunosuppressive microenvironment and represents a promising diagnostic marker and therapeutic target.

Indexed as

BiomarkerImmune functionNT5DC2Pan-cancerTNBC

Identifiers

PMID40591089
PMCPMC12214195

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