Evidence map›Paper›PMID 31880256›Full record

ArticleCurrent pharmaceutical biotechnology2020

Assessment of Expression of Homeobox A5 in Endometrial Cancer on the mRNA and Protein Level.

Konrad Dziobek, Marcin Oplawski, Nikola Zmarzły, Beniamin O Gabarek, Robert Kiełbasiński, Kamil Kiełbasiński, Przemysław Kieszkowski, Karol Talkowski, Dariusz Boroń

Open access · hybridAbstract read
In one paragraph

Article in Current pharmaceutical biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 1 country.

Konrad DziobekMaria Sklodowska-Curie National Research Institute of Oncology Krakow Branch, 11 Garncarska st. 31-115 Krakow, Poland.
Marcin OplawskiDepartment of Gynecology and Obstetrics with Gynecologic Oncology, Ludwik Rydygier Memorial Specialized Hospital, Krakow, Poland.
Nikola ZmarzłyDepartment of Histology, Cytophysiology and Embryology, Faculty of Medicine in Zabrze, University of Technology in Katowice, Zabrze, Poland.
Beniamin O GabarekMaria Sklodowska-Curie National Research Institute of Oncology Krakow Branch, 11 Garncarska st. 31-115 Krakow, Poland.
Robert KiełbasińskiDepartment of Obstetrics & Gynaecology Ward, Health Center in Mikolow, Mikolow, Poland.
Kamil KiełbasińskiPavol Jozef Šafárik University in Košice, Košice, Slovak Republic.
Przemysław KieszkowskiVoivodeship Specialist Hospital in Wloclawek, Wloclawek, Poland.
Karol TalkowskiPsychiatric Hospital in Olsztyn, Olsztyn, Poland.
Dariusz BorońMaria Sklodowska-Curie National Research Institute of Oncology Krakow Branch, 11 Garncarska st. 31-115 Krakow, Poland.
The Maria Sklodowska-Curie National Research Institute of Oncology · PLCuiavian University · PLMedical University of Silesia · PLUniversity of Computer Sciences and Economics in Olsztyn · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndometrial cancer is one of the most common gynecological cancer in the developed countries and occurs mainly in postmenopausal women. Angiogenesis is important for cancer formation as it provides nutrients for growing tumor mass. Most tumors do not show detectable Homeobox A5 (HOXA5 level), suggesting its potential role as a cancer suppressor. It was demonstrated that HOXA5 is involved in the progression of various types of cancer and the loss of its expression correlates with higher pathological grade and poorer outcome.

objectiveThe aim of the study was to evaluate HOXA5 expression at transcriptome and protein levels. MATERIALS AND

methodsThe study enrolled 45 women diagnosed with endometrial cancer and 15 without neoplastic changes. The histopathological examination allowed us to divide cancer tissue samples according to the degree of histological differentiation: G1, 17; G2, 15; G3, 13. The expression of the HOXA5 protein was determined by immunohistochemistry. Microarray and RT-qPCR techniques were used to assess HOXA5 expression at the mRNA level.

resultsThe reaction to the HOXA5 protein was only visible in glandular cells in G1 endometrial cancer and was lower compared to the control. In grades 2 and 3, reactions were noted at the limit of the method's sensitivity. In addition, reduced HOXA5 expression was observed at the transcriptome level.

conclusionHOXA5 may become a potential complementary molecular marker, allowing early detection of neoplastic changes in the endometrium. It also seems that detection of HOXA5 at the mRNA and protein levels may be helpful in improving the accuracy of diagnosis and planning effective oncological therapy.

Indexed as

Transcription, GeneticCell DifferentiationEndometrial NeoplasmsFemaleHomeodomain ProteinsHumansImmunohistochemistryMiddle AgedNeovascularization, PathologicRNA, MessengerHomeodomain ProteinsHOXA5 protein, humanRNA, MessengerEndometrial cancerHOXA5immunohistochemistrymicroarray.mRNA levelRT-qPCR

Identifiers

PMID31880256
PMCPMC7403687
OpenAlexW2997880707

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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.