Evidence map›Paper›PMID 39623306›Full record

ArticleBMC cancer2024

TRAIP enhances progression of tongue squamous cell carcinoma through EMT and Wnt/β-catenin signaling by interacting with DDX39A.

Litong Liu, Ping Wang, Cheng Guo, Li Song, Lifang Chen, Hongbing Qi, Yangyang Zheng, Xiaoming Xing, Chengqin Wang

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Article
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  3. 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

9 authors.

Litong Liu *Department of Pathology, School of Basic Medicine, Qingdao University, Ningxia Road No. 308, Qingdao, Shandong, 266071, China.
Ping Wang *Department of Pathology, Linyi People's Hospital, Linyi, 276000, Shandong, China.
Cheng Guo *Department of Pathology, School of Basic Medicine, Qingdao University, Ningxia Road No. 308, Qingdao, Shandong, 266071, China.
Li SongDepartment of Pathology, School of Basic Medicine, Qingdao University, Ningxia Road No. 308, Qingdao, Shandong, 266071, China.
Lifang ChenDepartment of Pathology, the Affiliated Hospital of Qingdao University, Qingdao, 266035, Shandong, China.
Hongbing QiDepartment of Pathology, the Affiliated Hospital of Qingdao University, Qingdao, 266035, Shandong, China.
Yangyang ZhengDepartment of Pathology, School of Basic Medicine, Qingdao University, Ningxia Road No. 308, Qingdao, Shandong, 266071, China.
Xiaoming XingDepartment of Pathology, the Affiliated Hospital of Qingdao University, Qingdao, 266035, Shandong, China.
Chengqin WangDepartment of Pathology, School of Basic Medicine, Qingdao University, Ningxia Road No. 308, Qingdao, Shandong, 266071, China. wcq0879@126.com.

Funding

Beijing Jingjian Pathology Development Foundation JJlXA2022-008the National Natural Science Foundation of China No.81672606the Natural Science Foundation of Shandong Province ZR2022MH206
6 · The paper itself

Abstract

backgroundTongue squamous cell carcinoma (TSCC) is one of the most common malignant tumors with high mortality and poor prognosis. Its incidence rate is increasing gradually. Tumor necrosis factor receptor-associated factor interacting protein (TRAIP), as a factor related to several tumors, reveals that its gene expression is different between normal tissue and primary tumor of head and neck squamous cell carcinoma using bioinformatics analysis.

methodIn our study, TCGA database, immunohistochemistry, proliferation assay, colony formation, wound healing assay, Transwell, cell cycle analysis and tumor xenografts model were used to determine the expression and functions of TRAIP in TSCC.

resultWe found that TRAIP may promote the proliferation, migration and invasion of TSCC. Furthermore, the results of bioinformatics analysis, mass spectrometry and co-immunoprecipitation suggested that DDX39A may be a TRAIP interacting protein. DDX39A has been proven to be an oncogene in several tumors, which may have an important effect on cell proliferation and metastasis in multiple tumors. In addition, the high expression of DDX39A implies the poor prognosis of patients. Our study demonstrated that TRAIP probably interact with DDX39A to regulate cell progression through epithelial-mesenchymal transition and Wnt/β-catenin pathway. In addition, we show that the necessary domain of DDX39A for the interaction between DDX39A and TRAIP region.

conclusionThese results indicate that TRAIP is important in occurrence and development of TSCC and is expected to become the new promising therapeutic target.

Indexed as

Cell MovementCell ProliferationDEAD-box RNA HelicasesDisease ProgressionEpithelial-Mesenchymal TransitionTongue NeoplasmsWnt Signaling PathwayAnimalsbeta CateninCarcinoma, Squamous CellCell Line, TumorGene Expression Regulation, NeoplasticHumansMiceMice, NudePrognosisbeta CateninDDX39A protein, humanDEAD-box RNA HelicasesDDX39AEMTProgressionTongue squamous cell carcinomaTRAIPWnt/β-catenin signaling

Identifiers

PMID39623306
PMCPMC11610093

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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.