Evidence map›Paper›PMID 37454079›Full record

ArticleBMC urology2023

Prognostic value of IKBIP in papillary renal cell carcinoma.

Huiling Zhang, Rui Tang, Xue Wen, Jingbo Cai, Juan Huang, Li Luo, Zhihui Yang

Open access · goldAbstract read
In one paragraph

Article in BMC urology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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

5 citing papers in PubMed, 5 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Huiling ZhangDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Rui TangDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Xue WenDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Jingbo CaiDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Juan HuangDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Li LuoDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China.
Zhihui YangDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, People's Republic of China. yzhih73@swmu.edu.cn.
Affiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundI kappa B kinase interacting protein, a highly conserved gene, has rarely been reported in cancer. According to previous study, IKBIP has only been shown to promote malignant progression of glioma. In other malignant tumors, few reports have examined the function of IKBIP, especially in papillary renal cell carcinoma. Therefore, the molecular profiles and clinical prognostic values of the IKBIP in papillary renal cell carcinoma remain undetermined.

methodsSeveral bioinformatic platforms and Immunohistochemistry were used to clarify the expression and prognostic values of IKBIP in Papillary renal cell carcinoma.

resultsIn this study, GEPIA and TIMER platform were used to identify mRNA expression of IKBIP in papillary renal cell carcinoma. And our results revealed that IKBIP mRNA expression was up-regulated in papillary renal cell carcinoma than in its corresponding normal tissues. In addition, high mRNA expression levels of IKBIP were correlated with age, pathological stage, pathological T stage and pathological N stage. Moreover, High IKBIP mRNA expression was negatively correlated with overall survival (OS) and disease-free survival (DFS) in patients of papillary renal cell carcinoma. Besides, Multivariate analysis indicated that IKBIP mRNA expression was an independent prognostic factor for patients of papillary renal cell carcinoma. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed IKBIP co-expressed genes were enriched in homologous recombination, DNA replication, cell cycle, Mismatch repair, Fanconi anemia pathway, P53 signaling pathway and nucleotide excision repair. And Immunohistochemical profile showed that protein expression of IKBIP was higher in papillary renal cell carcinoma than adjacent normal tissue.

conclusionsOverall, our findings reveled that IKBIP may act as a novel and potential tumor factor to accelerate papillary renal cell carcinoma progression, meanwhile, IKBIP could serve as a promising target for treating papillary renal cell carcinoma.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsBiomarkers, TumorHumansPrognosisRNA, MessengerBiomarkers, TumorRNA, MessengerBioinformaticsIKBIPPapillary renal cell carcinomaPrognosisSignaling pathway

Identifiers

PMID37454079
PMCPMC10349435
OpenAlexW4384405918

What OpenQuestion holds

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LicenceCC BY
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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.