Evidence map›Paper›PMID 24992025›Full record

ArticlePloS one2014

Multiple-integrations of HPV16 genome and altered transcription of viral oncogenes and cellular genes are associated with the development of cervical cancer.

Xulian Lu, Qiaoai Lin, Mao Lin, Ping Duan, Lulu Ye, Jun Chen, Xiangmin Chen, Lifang Zhang, Xiangyang Xue

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  9. MicroRNA miR-16-1 regulates CCNE1 (cyclin E1) gene expression in human cervical cancer cells.International journal of clinical and experimental medicine · 2015
    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

9 authors at 2 institutions in 1 country.

Xulian LuDepartment of Microbiology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China; Department of Pathology, Zhuji People's Hospital of Zhejiang Province, Zhuji, Zhejiang, China.
Qiaoai LinDepartment of Microbiology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Mao LinDepartment of Microbiology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China; Fuda Cancer Hospital Affiliated to the Medical College of Jinan University, Guangzhou, Guangdong, China.
Ping DuanDepartment of Obstetrics and Gynecology, Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Lulu YeInstitute of Molecular Virology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Jun ChenDepartment of Microbiology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xiangmin ChenSchool of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Lifang ZhangDepartment of Microbiology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xiangyang XueInstitute of Molecular Virology and Immunology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Wenzhou Medical University · CNFuda Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The constitutive expression of the high-risk HPV E6 and E7 viral oncogenes is the major cause of cervical cancer. To comprehensively explore the composition of HPV16 early transcripts and their genomic annotation, cervical squamous epithelial tissues from 40 HPV16-infected patients were collected for analysis of papillomavirus oncogene transcripts (APOT). We observed different transcription patterns of HPV16 oncogenes in progression of cervical lesions to cervical cancer and identified one novel transcript. Multiple-integration events in the tissues of cervical carcinoma (CxCa) are significantly more often than those of low-grade squamous intraepithelial lesions (LSIL) and high-grade squamous intraepithelial lesions (HSIL). Moreover, most cellular genes within or near these integration sites are cancer-associated genes. Taken together, this study suggests that the multiple-integrations of HPV genome during persistent viral infection, which thereby alters the expression patterns of viral oncogenes and integration-related cellular genes, play a crucial role in progression of cervical lesions to cervix cancer.

Indexed as

Gene Expression Regulation, NeoplasticGene Expression Regulation, ViralGenome, ViralFemaleHuman papillomavirus 16HumansOncogene ProteinsPapillomavirus InfectionsUterine Cervical NeoplasmsViral ProteinsOncogene ProteinsViral Proteins

Identifiers

PMID24992025
PMCPMC4081011
OpenAlexW1981068685

What OpenQuestion holds

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LicenceCC BY
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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.