Evidence map›Paper›PMID 35342765›Full record

ArticleBioMed research international2022

Determination of Human Papillomavirus Type 18 Lineage of E6: A Population Study from Iran.

Mona Sadat Larijani, Mir Davood Omrani, Rahim Soleimani, Anahita Bavand, Amir Houshang Nejadeh, Vahid Ezzatizadeh, Mahboubeh Jamshidi, Amitis Ramezani

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 10 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

8 authors at 3 institutions in 1 country.

Mona Sadat LarijaniClinical Research Department, Pasteur Institute of Iran, Tehran, Iran.ORCID https://orcid.org/0000-0003-3681-5319
Mir Davood OmraniDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-0673-9717
Rahim SoleimaniDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-7696-8830
Anahita BavandClinical Research Department, Pasteur Institute of Iran, Tehran, Iran.ORCID https://orcid.org/0000-0002-1894-6764
Amir Houshang NejadehAyandeh Clinical and Genetic Laboratory, Varamin, Iran.ORCID https://orcid.org/0000-0003-0698-690X
Vahid EzzatizadehAyandeh Clinical and Genetic Laboratory, Varamin, Iran.ORCID https://orcid.org/0000-0001-5232-4259
Mahboubeh JamshidiAyandeh Clinical and Genetic Laboratory, Varamin, Iran.ORCID https://orcid.org/0000-0001-5970-0608
Amitis RamezaniClinical Research Department, Pasteur Institute of Iran, Tehran, Iran.ORCID https://orcid.org/0000-0003-3502-8524
Pasteur Institute of Iran · IRShahid Beheshti University of Medical Sciences · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epidemiological studies in Iran on HPV18 nucleotide changes are rare. This type of virus is prevalent in the Iranian population. Therefore, in the present study, we aimed to identify the genetic variability in HPV18 in the E6 region to evaluate the prevalence of lineage distribution and sublineages in a sample population in Iran. Overall, 60 HPV18 confirmed cases were investigated between 2019 and 2021. The specimens were collected, and molecular genotyping was done using the Linear Array HPV Genotyping Test. DNA extraction was performed by a viral DNA/RNA kit. The HPV E6 gene was amplified by using type-specific primers designed according to the HPV18 genome prototype sequence. The sequencing of the E6 region was successfully done on 43 samples which were then compared to the reference sequence. The most frequent sublineage of HPV18 in this study was A4 (69.7%), followed by A1 (18.6%) and A3 (11.6%). Neither A2 nor A5 sublineage was not detected in this study. The related nucleotide acid changes according to the main references were as follows: A3: T104C/T232G/T485C/C549A, A4: T104C/T485C/C549A. The predominance of A lineage with the high frequency of A4 sublineage was found in the present research. The importance of sublineages in susceptibility to a progressive form of infection requires to be more investigated among the different population.

Indexed as

Oncogene Proteins, ViralPapillomavirus InfectionsUterine Cervical NeoplasmsFemaleGenetic VariationHuman papillomavirus 18HumansIranNucleotidesPhylogenyNucleotidesOncogene Proteins, Viral

Identifiers

PMID35342765
PMCPMC8956376
OpenAlexW4220776476

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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.