Evidence map›Paper›PMID 42365149›Full record

ArticleDiscover oncology2026

Pan-cancer prioritization of CCDC69 reveals an immune-enriched and therapeutically sensitive breast cancer phenotype.

Yi Chen, Boyang Li, Jinghao Pan, Ruonan Lin, Lucy Yue Lau, Boxiang Zhang, Kuan Wang, Chenlu Fang, Wenjia Guo, Zehao Hong

Abstract read
In one paragraph

Article in Discover oncology, 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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0citing papers 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

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Yi Chen *Cancer Research Institute, The Affiliated Cancer Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China.
Boyang Li *Cancer Research Institute, The Affiliated Cancer Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China.
Jinghao PanThe First Clinical School of Medicine, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Ruonan LinThe First Clinical School of Medicine, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Lucy Yue LauDepartment of Public Health, Harvard Medical School, Boston, MA, 02115, USA.
Boxiang ZhangCancer Research Institute, The Affiliated Cancer Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China.
Kuan WangCancer Research Institute, The Affiliated Cancer Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China.
Chenlu FangThe First Clinical School of Medicine, Zhengzhou University, Zhengzhou, 450052, Henan, China.
Wenjia GuoCancer Research Institute, The Affiliated Cancer Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China. wenjiaguoxjmu@163.com.
Zehao HongCancer Research Institute, The Affiliated Cancer Hospital of Xinjiang Medical University, Urumqi, 830011, Xinjiang Uygur Autonomous Region, China. HongZehaoZZU@outlook.com.

Funding

2022 Tianchi Young Talent Doctoral Program 2022TCYCGWJKey R&D Program in Xinjiang Uygur Autonomous Region 2022B03019-4Scientific Research and Innovation Team Project of Xinjiang Medical University XYD-2024C09
6 · The paper itself

Abstract

backgroundCoiled-coil domain-containing protein 69 (CCDC69) has been implicated in tumor biology, but its pan-cancer immunogenomic context and relevance to breast cancer remain insufficiently defined.

methodsWe integrated The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) transcriptomes, paired tumor-normal comparisons, diagnostic modeling, survival analyses, copy-number and genomic-instability profiling, immune-cycle and immune-infiltration analyses, single-cell and spatial transcriptomic datasets, pathway enrichment, immunotherapy cohorts, pharmacogenomic resources and molecular docking to characterize CCDC69 across cancers and in breast invasive carcinoma (BRCA).

resultsCCDC69 was broadly dysregulated across cancers and showed cancer-type-dependent diagnostic value. Pan-cancer survival analyses revealed context-specific prognostic effects, with BRCA showing consistent favorable associations for disease-specific survival (DSS), disease-free interval (DFI) and progression-free interval (PFI). Further analyses linked CCDC69 to copy-number states, stemness, genomic instability and multiple immune phenotypes. Integrated prioritization highlighted BRCA as a representative tumor context. In BRCA, higher CCDC69 expression was associated with less advanced clinicopathological features, immune-enriched microenvironments, increased cancer-immunity-cycle activity, diverse immune-cell infiltration and compartment-specific expression across tumor, immune and stromal regions. Pathway analyses connected CCDC69 with immune activation, interferon response and lymphocyte-related programs, while showing inverse associations with proliferation, DNA repair and cell-cycle signatures. Immunotherapy and drug-sensitivity analyses suggested context-dependent response-stratification and therapeutic relevance.

conclusionCCDC69 delineates an immune-active, favorable-risk BRCA state with potential prognostic and therapy-related value, warranting experimental and clinical validation.

Indexed as

Breast cancerCCDC69Immunotherapy responsePan-cancer analysisPrognostic biomarker

Identifiers

PMID42365149
PMCPMC13486434

What Socratic 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 Socratic graph.