Evidence map›Paper›PMID 41142627›Full record

ArticleFrontiers in oncology2025

CLIC6's role in cancer: from broad analysis to breast cancer validation.

Junyi Wang, Yiyang Wang, Haotian Ma, Yongxiang Li, Jiayue Hou, Jiaqi Li, Dilimulati Ismtula, Chenming Guo

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Intratumoral PD-1Medical oncology (Northwood, London, England) · 2026
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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

8 authors.

Junyi Wang *Department of Breast Surgery, Center of Digestive and Vascular, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yiyang Wang *Department of Breast Surgery, Center of Digestive and Vascular, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Haotian Ma *Department of Breast Surgery, Center of Digestive and Vascular, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Yongxiang LiDepartment of Breast Surgery, Center of Digestive and Vascular, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Jiayue HouClinical Medicine Department, Xinjiang Medical University, Urumqi, China.
Jiaqi LiClinical Medicine Department, Xinjiang Medical University, Urumqi, China.
Dilimulati IsmtulaDepartment of Breast Surgery, Center of Digestive and Vascular, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Chenming GuoDepartment of Breast Surgery, Center of Digestive and Vascular, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chloride Intracellular Channel 6 (CLIC6) is a potential cancer therapy target due to its close association with tumor development. However, its diagnostic and prognostic roles, as well as its impact on immune regulation in different cancers, remain unclear. Methods: This study utilized public databases like TCGA and GEO to analyze CLIC6 expression, diagnostic value, and prognostic significance across various cancers. It examined genetic and epigenetic variations, immune correlations, and performed functional enrichment analysis to uncover CLIC6-related pathways. Western blotting confirmed CLIC6 protein levels in breast cancer samples, while CCK-8, colony formation, transwell, and scratch assays evaluated its role in cell proliferation and migration. Tissue microarray and immunohistochemistry further validated CLIC6 expression in breast cancer. Results: Research shows that CLIC6 expression is typically lower in most cancers compared to normal tissues, with distinct patterns across different stages. It serves as a useful diagnostic marker and potential prognostic factor for BRCA, LUAD, STAD, and LGG. CLIC6 mutations are common in many cancers and affect prognosis. In most tumors, CLIC6 expression correlates with m6A methylation, and its promoter is highly methylated. In BRCA, the expression of CLIC6 is related to bacterial defense, immune response, endopeptidase regulation, neuropeptide signaling, and amino acid transport. It is expressed at low levels in BRCA tissues, and we speculate that a higher CLIC6 expression may be protective. Conclusion: In conclusion, CLIC6 can serve as a key biomarker for various cancers, and its expression level is related to the tumor immune microenvironment and the outcomes in selected cancers; further validation is warranted. Our research on CLIC6 in BRCA has revealed new potential for tumor treatment strategies targeting this marker.

Indexed as

CLIC6diagnosismethylationpan-cancerprognosistumor immunity

Identifiers

PMID41142627
PMCPMC12545143

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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.