Evidence map›Paper›PMID 36430789›Full record

ArticleInternational journal of molecular sciences2022

Esophageal Squamous Cancer from 4NQO-Induced Mice Model: CNV Alterations.

Zhiwei Liu, Ruibing Su, Anil Ahsan, Chencai Liu, Xiaoqi Liao, Dongping Tian, Min Su

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Zhiwei LiuGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.
Ruibing SuGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.ORCID 0000-0001-5594-4808
Anil AhsanGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.ORCID 0000-0001-9105-8272
Chencai LiuGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.
Xiaoqi LiaoGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.
Dongping TianGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.
Min SuGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Department of Pathology, Institute of Clinical Pathology, Shantou University Medical College, Shantou 515031, China.
Shantou University · CN

Funding

Innovative Team Grant of Guangdong Department of Education 2020KCXTD033National Natural Science Foundation of China (82073290, 81772997)
6 · The paper itself

Abstract

Squamous esophageal carcinoma is a common pathological type of esophageal carcinoma around the world. The prognosis of esophageal carcinoma is usually poor and diagnosed at late stages. Recently, research suggested that genomic instability occurred in esophageal cells during the development of esophageal squamous cell carcinoma (ESCC). Identifying prognostic and specific genomic characteristics, especially at the early hyperplasia stage, is critical. Mice were given 4-nitroquinoline 1-oxide (4NQO) with drinking water to induce esophageal cancer. The immortalized human esophageal epithelial cell line (NE2) was also treated with 4NQO. We performed histologic analyses, immunofluorescence, and immunohistochemical staining to detect DNA damage at different time points. Whole-exome sequencing was accomplished on the esophagus tissues at different pathological stages to detect single-nucleotide variants and copy number variation (CNV) in the genome. Our findings indicate that all mice were tumor-forming, and a series of changes from simple hyperplasia (ESSH) to intraepithelial neoplasia (IEN) to esophageal squamous cell carcinoma (ESCC) was seen at different times. The expression of γ-H2AX increased from ESSH to ESCC. In addition, mutations of the

Indexed as

Carcinoma, Squamous CellEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaAnimalsDNA Copy Number VariationsHumansHyperplasiaMice4NQOcopy number variationsDNA damageesophageal squamous cell carcinomasingle-nucleotide variantswhole-exome sequence

Identifiers

PMID36430789
PMCPMC9698903
OpenAlexW4309287318

What OpenQuestion holds

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LicenceCC BY
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.