Evidence map›Paper›PMID 42487720›Full record

ArticleAmerican journal of clinical and experimental immunology2026

Expression and prognostic significance of CRKL in clear cell renal cell carcinoma.

Jinxia Wang, Ye Yang, Xiao Yuan, Weichen Wang

Abstract read
In one paragraph

Article in American journal of clinical and experimental immunology, 2026. 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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jinxia WangDepartment of Clinical Laboratory, Binzhou Medical University Hospital Binzhou 256603, Shandong, China.
Ye YangDepartment of Clinical Laboratory, Binzhou Medical University Hospital Binzhou 256603, Shandong, China.
Xiao YuanDepartment of Clinical Laboratory, Binzhou Medical University Hospital Binzhou 256603, Shandong, China.
Weichen WangDepartment of Clinical Laboratory, Binzhou Medical University Hospital Binzhou 256603, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is an aggressive kidney malignancy with limited prognostic biomarkers. CRKL has been implicated in cancer progression, but its prognostic value and immune associations in ccRCC remain unclear. Using TCGA, GEO, and UALCAN databases, we analyzed CRKL expression. Kaplan-Meier and multivariate Cox regression assessed survival; TIMER and TISIDB evaluated immune infiltration; LinkedOmics databases and GSEA identified enriched pathways. CRKL was significantly overexpressed in ccRCC tissues at both mRNA and protein levels. Surprisingly, high CRKL expression was associated with better overall survival (OS), disease-specific survival (DSS), progression-free interval (PFI), and disease free survival (DFS). Multivariate Cox analysis identified CRKL as an independent favorable prognostic factor (OS: HR = 0.469, 95% CI: 0.302-0.729, P < 0.001). CRKL positively correlated with immune cell infiltration and immune-related pathways. In conclusion, CRKL is overexpressed in ccRCC, paradoxically, higher expression predicts better prognosis and is associated with immune-active tumor microenvironment features. These findings suggest that the favorable prognosis associated with CRKL may be attributable to its immunomodulatory role within the tumor microenvironment, highlighting its potential as a novel prognostic biomarker for ccRCC.

Indexed as

bioinformaticsclear cell renal cell carcinoma (ccRCC)CRKLimmune infiltrationprognosis

Identifiers

PMID42487720
PMCPMC13389482

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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.