Evidence map›Paper›PMID 36073321›Full record

ArticleThoracic cancer2022

Promotor methylation status of MAPK4 is a novel epigenetic biomarker for prognosis of recurrence in patients with thymic epithelial tumors.

Wei Guan, Songlin Li, Zhimin Zhang, He Xiao, Juan He, Jian Li, Xuan He, Jia Luo, Yun Liu, Lin Lei and 3 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 27% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Methods in DNA methylation array dataset analysis: A review.Computational and structural biotechnology journal · 2024
    Review
  3. Heliyon · 2024
    Article
  4. The Molecular Landscape of Thymic Epithelial Tumors: A Comprehensive Review.International journal of molecular sciences · 2024
    Review
  5. Review
  6. 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

13 authors at 3 institutions in 2 countries.

Wei Guan *Department of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Songlin Li *Cancer Center, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Zhimin Zhang *Cancer Center, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
He XiaoDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.ORCID 0000-0003-2298-1121
Juan HeDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Jian LiDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Xuan HeDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Jia LuoDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Yun LiuDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Lin LeiDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Jungang MaDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.
Lizhao ChenDepartment of Neurosurgery, Daping Hospital, Army Medical University, Chongqing, China.
Chuan ChenDepartment of Cancer Center, Daping Hospital, Army Medical University, Chongqing, China.ORCID 0000-0003-0047-9560
Army Medical University · CNUniversity of Electronic Science and Technology of China · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognosis of thymic epithelial tumors (TETs) currently relies on the commonly adopted WHO classification and Masaoka staging system, which cannot reflect the undefined biological behaviors limiting them as prognostic factors.

methodsIn this study, we first identified 40 genes and 179 genes, respectively that were epigenetically upregulated and silenced, corresponding to a total of 509 functionally methylated CpG sites between thymomas and thymic carcinomas by using the TCGA dataset.

resultsThe methylation β-values of cg20068620 in MAPK4 and cg18770944 in USP51 were significantly associated with recurrence-free survival (RFS). In the independent validation cohort, only WHO classification and methylation β-values of cg20068620 in MAPK4 were independent prognostic factors for RFS in Chinese patients with TETs. A linear weighted model including these two factors was used to calculate the recurrence risk score (RRS). Time-dependent ROC curve analysis revealed that RRS was overwhelmingly superior to WHO classification for predicting 3-, 5-, and 10-year RFS and Masaoka stage for 3- and 5-year RFS.

conclusionsThese results suggested that the methylation site cg20068620 in MAPK4 can improve the accuracy of the WHO classification alone regarding the prognostic value of TETs recurrence.

Indexed as

Neoplasms, Glandular and EpithelialRNA HelicasesThymomaThymus NeoplasmsBiomarkersDNA MethylationEpigenesis, GeneticHumansNeoplasm Recurrence, LocalPrognosisPromoter Regions, GeneticUbiquitin-Specific ProteasesBiomarkersMAPK4 protein, humanRNA HelicasesUbiquitin-Specific ProteasesUSP51 protein, humanDNA methylationprognosispyrosequencingrecurrencethymic epithelial tumors

Identifiers

PMID36073321
PMCPMC9575130
OpenAlexW4294992641

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.