Evidence map›Paper›PMID 30615540›Full record

ArticleJournal of global oncology2019

HES1 Protein Modulates Human Papillomavirus-Mediated Carcinoma of the Uterine Cervix.

Richa Tripathi, Gayatri Rath, Vishwas Sharma, Showket Hussain, Shashi Sharma, Mausumi Bharadwaj, Ravi Mehrotra

Open access · goldAbstract read
In one paragraph

Article in Journal of global oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 6 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 3 institutions in 1 country.

Richa TripathiIndian Council of Medical Research-National Institute of Cancer Prevention and Research, Noida, India.
Gayatri RathVardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Vishwas SharmaIndian Council of Medical Research-National Institute of Cancer Prevention and Research, Noida, India.
Showket HussainIndian Council of Medical Research-National Institute of Cancer Prevention and Research, Noida, India.
Shashi SharmaIndian Council of Medical Research-National Institute of Cancer Prevention and Research, Noida, India.
Mausumi BharadwajIndian Council of Medical Research-National Institute of Cancer Prevention and Research, Noida, India.
Ravi MehrotraIndian Council of Medical Research-National Institute of Cancer Prevention and Research, Noida, India.
Indian Council of Medical Research · INNational Institute of Cancer Prevention and Research · INVardhman Mahavir Medical College & Safdarjung Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCervical cancer (CC) is the most common cancer affecting women worldwide. Human papillomavirus (HPV) infection is a major contributing factor for the development of CC. The development of CC occurs progressively from precancer stages to cancerous stages (ie, invasive squamous cell carcinoma [ISCC] and adenocarcinoma [ADC]). ADC is a rare form of CC that develops from the mucinous endocervical epithelium. It is believed that the downstream targets of Notch signaling contribute to the etiology of CC. One such target is HES1, whose role in the modulation of ADC is unknown. The purpose of this study is to determine the role of HES1 protein in HPV-associated ADC subtype of CC and also to compare its expression in histologic subtypes of precancer and ISCC. PATIENTS AND

methodsA total of 148 patients (30 with precancers, 98 with ISCC, and 20 with ADC) and 40 normal control participants were analyzed for the expression of HES1 via immunohistochemistry, with results validated by immunoblotting.

resultsThe comparison between HPV-16 and HES1 expression was significant in precancer (cervical intraepithelial neoplasia grades 1 to 3; P = .013), ISCC (International Federation of Gynecology and Obstetrics stages I to IV; P = .001), and ADC ( P = .007). An overall significant mean difference was observed between HES1, JAG1, and Notch-3 proteins in precancer ( P = .001), ISCC ( P = .001), and ADC ( P = .001). Pairwise comparisons between HES1 and JAG1 and HES1 and Notch-3 were also found to be significant.

conclusionThis study showed that among all HPV-16-positive precancers, the major HES1 positivity signal arises from cervical intraepithelial neoplasia grades 2 and 3 that develops into ISCC. Moreover, HPV-16-positive ADC also showed an association with HES1. The HES1, JAG1, and Notch-3 proteins showed their synergistic role in modulating HPV associated ADC along with histologic subtypes of precancer and ISCC of CC.

Indexed as

Carcinoma, Squamous CellCase-Control StudiesFemaleHumansImmunohistochemistryNeoplasm StagingPapillomaviridaePapillomavirus InfectionsPrecancerous ConditionsReceptor, Notch3ROC CurveTranscription Factor HES-1Uterine Cervical DysplasiaUterine Cervical NeoplasmsHES1 protein, humanNOTCH3 protein, humanReceptor, Notch3Transcription Factor HES-1

Identifiers

PMID30615540
PMCPMC6426524
OpenAlexW2909849544

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.