Evidence map›Paper›PMID 36551704›Full record

ArticleCancers2022

Comprehensive Analysis of DMRT3 as a Potential Biomarker Associated with the Immune Infiltration in a Pan-Cancer Analysis and Validation in Lung Adenocarcinoma.

Donghong Yang, Meilian Liu, Junhong Jiang, Yiping Luo, Yongcun Wang, Huoguang Chen, Dongbing Li, Dongliang Wang, Zhixiong Yang, Hualin Chen

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  7. Interferon Epsilon Loss Is Elusive 9p21 Link to Immune-Cold Tumors, Resistant to Immune Checkpoint Therapy, and Endogenous CXCL9/10 Induction.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Review
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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

10 authors.

Donghong YangDepartment of Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Meilian LiuDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Junhong JiangDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Yiping LuoDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Yongcun WangDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Huoguang ChenDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Dongbing LiDepartment of Medicine, ChosenMed Technology (Beijing) Co., Ltd., Beijing 100176, China.ORCID 0000-0002-5227-9643
Dongliang WangDepartment of Medicine, ChosenMed Technology (Beijing) Co., Ltd., Beijing 100176, China.
Zhixiong YangDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.
Hualin ChenDepartment of Pulmonary Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.ORCID 0000-0003-1225-6284

Funding

Medical Research Fund of Guangdong Province in 2020 A2020500
6 · The paper itself

Abstract

Doublesex and Mab-3 related Transcription Factor 3 (DMRT3) is associated with the prognosis of some tumors. It is possible to explore the role of DMRT3 in the cancer process using bioinformatic approaches and experimental validation. We comprehensively explored the clinical and immunological characteristics of DMRT3. The DMRT3 expression is abnormal in human cancers and correlates with clinical staging. A high DMRT3 expression is significantly associated with poor overall survival (OS) in KIRC, KIRP, LUAD, and UCEC. Amplification was the greatest frequency of the DMRT3 alterations in pan-cancer. The OS was significantly lower in the DMRT3 altered group than in the DMRT3 unaltered group (P = 0.0276). The DMRT3 expression was significantly associated with MSI in three cancer types and TMB in six cancer types. The DMRT3 expression was significantly correlated with the level of the immune cell infiltration and the immune checkpoint genes. The DMRT3 was involved in some pathways in pan-cancer. DMRT3 may play a role in chemotherapy and may be associated with chemoresistance. A ceRNA network of KCNQ1OT1/miR-335-5p/DMRT3 was constructed in LUAD. DMRT3 was significantly upregulated in the LUAD cell lines. DMRT3 was aberrantly expressed in pan-cancer and may promote tumorigenesis and progression via different mechanisms. DMRT3 can be used as a therapeutic target to treat cancer in humans.

Indexed as

DMRT3genomic alterationsimmunepan-cancerprognosis

Identifiers

PMID36551704
PMCPMC9777283

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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.