Evidence map›Paper›PMID 39469683›Full record

ArticleHeliyon2024

ZBP1 as a prognostic biomarker correlated with cell proliferation in clear cell renal cell carcinoma.

Yuqing Zhang, Tao Wang, Daniyaerjiang Mutailipu, Yang Li, Shengjie Liang, Qingtong Yi, Rujian Zhu, Junjie Ma

Abstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

8 authors.

Yuqing ZhangDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Tao WangDepartment of Urology, Soochow University Affiliated Taicang Hospital (The First People's Hospital of Taicang), Taicang, China.
Daniyaerjiang MutailipuDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Yang LiDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Shengjie LiangDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Qingtong YiDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Rujian ZhuDepartment of Urology, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai, China.
Junjie MaDepartment of Urology, Soochow University Affiliated Taicang Hospital (The First People's Hospital of Taicang), Taicang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Z-DNA-binding protein 1 (ZBP1) is a critical Z-DNA- and Z-RNA-binding protein. However, its diagnostic and prognostic significance, as well as its functions in clear cell renal cell carcinoma (ccRCC), are not well understood. Materials and methods: Paired and unpaired differential expression analyses of ZBP1 were performed in pan-cancer cells. Receiver operating characteristic (ROC) curves and survival analyses were used to evaluate the clinical significance of ZBP1. Functional enrichment and immune infiltration analyses were used to explore the mechanisms underlying ZBP1 expression. Western blotting, qRT-PCR, CCK-8, and colony formation assays were used to investigate the potential function of ZBP1 in ccRCC cells. Molecular docking was utilized to identify drugs targeting ZBP1. Results: ZBP1 was highly expressed in ccRCC, demonstrating significant diagnostic and prognostic value. ZBP1 mRNA expression correlated with TNM stage, pathologic stage, and histologic grade. Functional enrichment analyses indicated that ZBP1 is involved in multiple immune processes. Moreover, ZBP1 mRNA expression was positively correlated with the infiltrating levels of T cells and cytotoxic cells, and negatively correlated with the infiltrating levels of mast cells and Th17 cells in ccRCC. Biological experiments confirmed that ZBP1 promotes ccRCC cell proliferation. Molecular docking studies identified rucaparib as a potential drug targeting ZBP1. Conclusion: Our research findings suggest that targeting ZBP1 could represent a novel therapeutic approach to inhibit the progression of ccRCC.

Indexed as

ccRCCImmune infiltrationPrognosisProliferationZBP1

Identifiers

PMID39469683
PMCPMC11513510

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.