Evidence map›Paper›PMID 31685833›Full record

ArticleScientific reports2019

Human papillomavirus and human telomerase RNA component gene in cervical cancer progression.

Yang Liu, Pianping Fan, Yingying Yang, Changjun Xu, Yajuan Huang, Daizhu Li, Qing Qing, Chunyi Sun, Honglin Zhou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 19 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

9 authors at 2 institutions in 1 country.

Yang LiuDepartment of Reproductive, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China.
Pianping FanDepartment of Gynecology, LinFen Central Hospital of Shanxi Province, LinFen, Shanxi, 041000, P.R. China.
Yingying YangDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China.
Changjun XuDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China.
Yajuan HuangDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China.
Daizhu LiDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China.
Qing QingDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China.
Chunyi SunDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China. 787413869@qq.com.
Honglin ZhouDepartment of Gynecology, the Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, 650101, P.R. China. km20150515@163.com.
Kunming Medical University · CNXian Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to examine hTERC gene in different grades of cervical intraepithelial neoplasia (CIN) and cervical cancer, and the association between hTERC and high risk-human papillomavirus (HR-HPV) infection. Patients who underwent cervical cancer screening at the Second Affiliated Hospital of Kunming Medical University between October 2010 and December 2011 were enrolled. All patients underwent liquid-based cytology test and hybrid capture 2 (HC2) for HPV detection. hTERC was examined using fluorescence in situ hybridization (FISH). Cervical colposcopy biopsy was performed if any of the three results was positive. HC2, FISH, and pathology were compared. A total of 1200 women underwent screening, 150 patients underwent cervical biopsy: 32 in the normal group, 38 in the CIN1 group, 66 in the CIN2/3 group, and 14 in the invasive cervical cancer group. More patients had HR-HPV infection in the CIN2/3 group and ICC group compared with the CIN1 group. hTERC increased with increasing histological dysplasia. There was significant difference in hTERC positive rate between each of the three groups. More patients with hTERC gene amplification were observed in the positive HR-HPV group than in the HR-HPV negative group. In conclusion, hTERC is a potential marker for precancerous cervical cancer lesions. hTERC might be correlated with HR-HPV infection in cervical diseases.

Indexed as

Disease ProgressionFemaleHumansIn Situ Hybridization, FluorescenceNucleic Acid Amplification TechniquesPapillomaviridaePapillomavirus InfectionsRNATelomeraseUterine Cervical DysplasiaUterine Cervical NeoplasmsRNATelomerasetelomerase RNA

Identifiers

PMID31685833
PMCPMC6828729
OpenAlexW2989350419

What OpenQuestion holds

Textmetadata
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.