Evidence map›Paper›PMID 31854042›Full record

ArticleCancer science2020

Ubiquitination of NOTCH2 by DTX3 suppresses the proliferation and migration of human esophageal carcinoma.

Xin-Yu Ding, Hai-Yang Hu, Ke-Nan Huang, Rong-Qiang Wei, Jie Min, Chen Qi, Hua Tang, Xiong Qin

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

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  11. A multidimensional pan-cancer analysis of DCAF13 and its protumorigenic effect in lung adenocarcinoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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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

8 authors at 3 institutions in 1 country.

Xin-Yu DingDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Hai-Yang HuDepartment of Thoracic Surgery, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ke-Nan HuangDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Rong-Qiang WeiDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Jie MinDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Chen QiDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Hua TangDepartment of Thoracic Surgery, Shanghai Changzheng Hospital, Second Military Medical University, Shanghai, China.
Xiong QinDepartment of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.ORCID https://orcid.org/0000-0003-3195-1821
Second Military Medical University · CNShanghai Jiao Tong University · CNTongji University · CN

Funding

National Natural Science Foundation of China 81402449
6 · The paper itself

Abstract

The NOTCH2 gene plays a role in the development of many tumors. Deltex E3 ubiquitin ligase 3 (DTX3) was identified as a novel E3 ligase for NOTCH2 and as a potential therapeutic target for esophageal cancer. However, whether DTX3 could regulate NOTCH2 to suppress the progression of esophageal carcinoma remains unknown. In our study, NOTCH2 had higher expression in human esophageal carcinoma cell lines compared to normal human esophageal epithelial cell line, and ablation of NOTCH2 suppressed the proliferation and migration of esophageal carcinoma cells. A novel E3 ligase for NOTCH2 was identified by yeast two-hybrid (Y2H) screening, and DTX3 promoted the ubiquitination and degradation of NOTCH2. Further study showed that DTX3 overexpression suppressed the proliferation and tumorigenicity of human oesophageal carcinoma cells. The analysis of tissue samples from patients revealed that the expression of NOTCH2 was high while the expression of DTX3 was low in esophageal cancer. Furthermore, the expression of DTX3 and NOTCH2 showed a significant negative correlation in human oesophageal cancer samples. Our study suggested that the DTX3-NOTCH2 axis plays an important role in the progression of esophageal cancer, and DTX3 acts as an anti-oncogene in esophageal carcinoma, potentially offering a therapeutic target for esophageal cancer.

Indexed as

AnimalsCell Line, TumorCell MovementCell ProliferationDisease ProgressionEsophageal NeoplasmsGene Expression Regulation, NeoplasticHumansMaleMiceNeoplasm InvasivenessNeoplasm TransplantationProteolysisReceptor, Notch2Signal TransductionUbiquitinationDTX3 protein, humanNOTCH2 protein, humanReceptor, Notch2Ubiquitin-Protein Ligasesanti-oncogeneDTX3esophageal carcinomaNOTCH2ubiquitination

Identifiers

PMID31854042
PMCPMC7004520
OpenAlexW2995161915

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.