Evidence map›Paper›PMID 34868367›Full record

ArticleOncology letters2022

Evaluation of dyskerin expression and the Cajal body protein WRAP53β as potential prognostic markers for patients with primary vaginal carcinoma.

Cecilia Ranhem, Gabriella Lillsunde Larsson, David Lindqvist, Bengt Sorbe, Mats G Karlsson, Marianne Farnebo, Kristina Hellman, Larysa Kovaleska, Elena Kashuba, Sonia Andersson

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Article in Oncology letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
–field-weighted citation impact, top 81% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 6 institutions in 2 countries.

Cecilia RanhemDepartment of Women's and Children's Health, Karolinska Institutet, 171 77 Stockholm, Sweden.
Gabriella Lillsunde LarssonSchool of Health and Medical Sciences, Örebro University, Campus USÖ, 701 82 Örebro, Sweden.
David LindqvistDepartment of Radiation Sciences, Umeå Universitet, 901 87 Umeå, Sweden.
Bengt SorbeDepartment of Oncology, Örebro University Hospital, 701 85 Örebro, Sweden.
Mats G KarlssonSchool of Medical Sciences, Örebro University, 701 85 Örebro, Sweden.
Marianne FarneboDepartment of Bioscience and Nutrition, Karolinska Institutet, 141 83 Stockholm, Sweden.
Kristina HellmanDepartment of Oncology-Pathology, Karolinska Institutet, 171 64 Stockholm, Sweden.
Larysa KovaleskaR.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology of National Academy of Sciences of Ukraine, 03022 Kiev, Ukraine.
Elena KashubaR.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology of National Academy of Sciences of Ukraine, 03022 Kiev, Ukraine.
Sonia AnderssonDepartment of Women's and Children's Health, Karolinska Institutet, 171 77 Stockholm, Sweden.
Karolinska Institutet · SEÖrebro University · SENational Academy of Sciences of Ukraine · UAÖrebro University Hospital · SER.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology · UAUmeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary vaginal cancer (PVC) is a rare gynaecological malignancy, which, at present, lacks appropriate biomarkers for prognosis. The proteins dyskerin and WD repeat containing antisense to TP53 (WRAP53β), both of which exert their functions in the telomerase holoenzyme complex, have been shown to be upregulated in different cancer types. These proteins have also been proposed as prognostic markers in some types of cancer. The aim of the present study was to examine the expression patterns of dyskerin and WRAP53β in patients with PVC. Moreover, as part of a search for effective biomarkers to evaluate prognosis in PVC, the expression of these two proteins and their potential association with clinical variables and survival were also evaluated. The expression of dyskerin and WRAP53β was assessed in PVC tumour samples from 68 patients using immunohistochemistry. The majority of tumour samples showed low and moderate expression levels of dyskerin. Upregulation of dyskerin in tumour samples was significantly associated with a shorter survival time and a poorer cancer-specific survival rate. WRAP53β was also expressed in most of the cells but was not significantly associated with clinical variables or survival. This study demonstrates that upregulation of dyskerin is significantly associated with poor prognosis. Thus, dyskerin may serve as a promising prognostic marker and a potential putative therapeutic target in PVC.

Indexed as

biomarkerCajal bodydyskerinprimary vaginal carcinomaprognosissurvivalWRAP53β

Identifiers

PMID34868367
PMCPMC8630817
OpenAlexW3216068338

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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.