Evidence map›Paper›PMID 30311151›Full record

ArticleDigestive diseases and sciences2019

The Clinicopathological Correlations of hTERC Amplification with Esophageal Squamous Cell Precursor Lesions.

Yanping Hu, Xiaojing Teng, Linlin Wu, Wei Liu, Jianduo An

Open access · hybridAbstract read
In one paragraph

Article in Digestive diseases and sciences, 2019. 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
0.5field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Signaling pathways and targeted interventions for precancers.Signal transduction and targeted therapy · 2026
    Review
  2. Non-canonical roles of canonical telomere binding proteins in cancers.Cellular and molecular life sciences : CMLS · 2021
    Review
  3. Annals of translational medicine · 2021
    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

5 authors at 2 institutions in 1 country.

Yanping HuDepartment of Pathology, Beijing LuHe Hospital, Capital Medical University, Beijing, 101149, China. yphu92@163.com.ORCID http://orcid.org/0000-0001-7128-2648
Xiaojing TengDepartment of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, China.
Linlin WuDepartment of Pathology, Beijing LuHe Hospital, Capital Medical University, Beijing, 101149, China.
Wei LiuDepartment of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, China.
Jianduo AnDepartment of Pathology, Beijing LuHe Hospital, Capital Medical University, Beijing, 101149, China.
Beijing Luhe Hospital Affiliated to Capital Medical University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEsophageal squamous cell precursor lesions remain one of the most controversial topics in pathology and clinical management.

aimsTo analyze the dysregulation of human telomerase RNA component (hTERC) in esophageal squamous cell precursor lesions and the clinicopathological correlations with the characteristics of esophageal squamous cell precursor lesions.

methodsFlorescence in situ hybridization was performed to detect hTERC amplification in different gradings of esophageal squamous cell precursor lesions. With retrospective follow-up data, clinicopathological correlations between hTERC and esophageal squamous cell precursor lesions were subjected to logistic regression analysis.

resultshTERC amplification gradually increased with upgrading of dysplasia, reaching the highest level in high-grade intraepithelial neoplasia, and there was a significant difference between the low-grade intraepithelial neoplasia group and the high-grade intraepithelial neoplasia group (P = 0.00). Logistic regression analysis showed that hTERC amplification was correlated with both dysplasia grading and ulcer characteristics of esophageal squamous cell precursor lesions (P < 0.05).

conclusionshTERC amplification with increasing grading of esophageal squamous cell precursor lesions and the presence of ulcer characteristics might provide an important molecular and pathological marker for the diagnosis and clinical prognosis of esophageal squamous cell precursor lesions, especially for those ambiguous cases with more divergence in classification.

Indexed as

Gene AmplificationAdultAgedAged, 80 and overBiomarkers, TumorBiopsyEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGenetic Predisposition to DiseaseHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedNeoplasm GradingPhenotypeBiomarkers, TumorRNATelomerasetelomerase RNAClinicopathological correlationDysplasiaEsophagealhTERCPremalignant lesionsUlcer

Identifiers

PMID30311151
PMCPMC6318245
OpenAlexW2897248846

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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.