Evidence map›Paper›PMID 40783572›Full record

ArticleNature communications2025

Non-coding genetic elements of lung cancer identified using whole genome sequencing in 13,722 Chinese.

Dan Zhou, Ming Wu, Qilong Tan, Liyang Sun, Yuanxing Tu, Weifang Zheng, Yun Zhu, Min Yang, Kejia Hu, Fang Hu and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

20 authors.

Dan Zhou *Center of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-5313-8164
Ming Wu *Department of Thoracic Surgery, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-1009-5387
Qilong Tan *Center of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Liyang SunThe Second Affiliated Hospital of Zhejiang University School of Medicine, Lanxi Branch (Lanxi People's Hospital), Lanxi, Zhejiang, China.
Yuanxing TuThe Second Affiliated Hospital of Zhejiang University School of Medicine, Lanxi Branch (Lanxi People's Hospital), Lanxi, Zhejiang, China.
Weifang ZhengLanxi Hospital of Traditional Chinese Medicine, Lanxi, Zhejiang, China.
Yun ZhuCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Min YangDepartment of Nutrition and Food Hygiene School of Public Health, and Center of Clinical Big Data and Analytics of The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Kejia HuCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-1175-3580
Fang HuCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Xiaohang XuCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Hanyi ZhouCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Tian LuoHIM-BGI Omics Center, BGI Research, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences (CAS), Hangzhou, China.
Fangming YangHIM-BGI Omics Center, BGI Research, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences (CAS), Hangzhou, China.
Fuqiang LiHIM-BGI Omics Center, BGI Research, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences (CAS), Hangzhou, China.ORCID http://orcid.org/0000-0002-2085-1457
Xin JinGuangdong Provincial Key Laboratory of Human Disease Genomics, Shenzhen Key Laboratory of Genomics, BGI Research, Shenzhen, China.ORCID http://orcid.org/0000-0001-7554-4975
Huakang TuCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Wenyuan LiCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0001-6196-9964
Kui WuHIM-BGI Omics Center, BGI Research, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences (CAS), Hangzhou, China. wukui@genomics.cn.ORCID http://orcid.org/0000-0002-6857-7231
Xifeng WuCenter of Clinical Big Data and Analytics of the Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China. xifengw@zju.edu.cn.ORCID http://orcid.org/0000-0003-2980-8129

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A substantial portion of lung cancer-associated genetic elements in East Asian populations remains unidentified, underscoring the need for large-scale genome-wide studies, particularly on non-coding regulation. We conducted a whole genome sequencing (WGS)-based genome-wide scan in 13,722 Chinese individuals to identify regulatory elements associated with lung cancer. We verified common-variant-based loci by meta-analysis across the available East Asian studies. Integrating a genome-transcriptome reference panel of lung tissue in 297 Chinese, we bridged the variant-lung cancer associations, highlighting genes including TP63 and DCBLD1. Implementing the STAAR pipeline for rare variant aggregate analysis, we identified and replicated novel genes, including PARPBP, PLA2G4C, and RITA1 in the context of non-coding regulation. Adapting a deep learning-based approach, potential upstream regulators such as TP53, MYC, ZEB1, and NFKB1 were revealed for the lung cancer-associated genes. These findings offered crucial insights into the non-coding regulation for the etiology of lung cancer, providing additional potential targets for intervention.

Indexed as

East Asian PeopleLung NeoplasmsChinaFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleNF-kappa B p50 SubunitTranscription FactorsTumor Suppressor ProteinsWhole Genome SequencingNF-kappa B p50 SubunitNFKB1 protein, humanTP63 protein, humanTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID40783572
PMCPMC12335547

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.