Evidence map›Paper›PMID 41331054›Full record

ArticleScientific reports2025

DHX36 plays an oncogenic role in breast cancer progression and invasiveness.

Chunli Wei, Dongmei Xu, Jingliang Cheng, Meiling Zheng, Ting Li, Jing Yang, Jiayue He, Ali H El-Far, Lianmei Zhang, Xiuli Xiao and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

12 authors.

Chunli Wei *Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Dongmei Xu *Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Jingliang Cheng *Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Meiling Zheng *Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Ting Li *Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Jing YangKey Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Jiayue HeKey Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Ali H El-FarKey Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China.
Lianmei ZhangDepartment of Pathology, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huai'an, 223300, Jiangsu Province, China.
Xiuli XiaoDepartment of Pathology, The Affiliated Hospital, Southwest Medical University, Luzhou, 646000, Sichuan Province, China.
Tao HeKey Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China. hetao198@swmu.edu.cn.
Junjiang FuKey Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, 319 Zhongshan Road, Luzhou, 646000, Sichuan Province, China. fujunjiang@swmu.edu.cn.

Funding

the Joint Innovation Special Project of Science and Technology Plan of Sichuan Province 2022YFS0623
6 · The paper itself

Abstract

DHX36 is an ATP-dependent DNA/RNA helicase that unwinds the guanine-quadruplexes (G4s) of DNA or RNA and regulates their metabolism for key biological functions. Breast cancer is a malignant tumor and effective targeted therapy drugs are limited, even though chemotherapy is generally used. In this study, we found that overexpression of DHX36 promotes breast cancer cell growth, migration, and invasion in vitro, while knocking down or knocking out reversed in vitro and in vivo. Moreover, DHX36 was highly expressed in most clinical breast tumor tissues compared with the matched healthy tissues. Accordingly, higher DHX36 expression correlated with poor recurrence-free survival (RFS) in the patients of breast cancer. These results substantiate that DHX36 might be a diagnostic and prognostic biomarker and is a proto-oncogene that promotes the growth and metastasis of breast cancer. Thus, targeting DHX36-associated G4s in genes, particularly in proto-oncogenes, might be a novel anticancer strategy.

Indexed as

Breast NeoplasmsDEAD-box RNA HelicasesAnimalsBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeNeoplasm InvasivenessPrognosisProto-Oncogene MasBiomarkers, TumorDEAD-box RNA HelicasesDHX36 protein, humanMAS1 protein, humanProto-Oncogene MasBreast cancerDHX36MetastasisOncogene

Identifiers

PMID41331054
PMCPMC12789463

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.