Evidence map›Paper›PMID 26556343›Full record

ReviewInternational journal of molecular sciences2015

Long Non-Coding RNAs in Endometrial Carcinoma.

Maria A Smolle, Marc D Bullock, Hui Ling, Martin Pichler, Johannes Haybaeck

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
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  7. Clinical application of liquid biopsy in endometrial carcinoma.Medical oncology (Northwood, London, England) · 2023
    Review
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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

5 authors at 3 institutions in 3 countries.

Maria A SmolleInstitute of Pathology, Medical University of Graz, Auenbruggerplatz 25, Graz A-8036, Austria. maria.smolle@stud.medunigraz.at.
Marc D BullockCancer Sciences, Faculty of Medicine, University of Southampton, Southampton SO171BJ, UK. bullockmd@yahoo.co.uk.
Hui LingDepartment of Experimental Therapeutics, the University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. hling@mdanderson.org.
Martin PichlerDivision of Clinical Oncology, Department of Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz A-8036, Austria. martin.pichler@medunigraz.at.
Johannes HaybaeckInstitute of Pathology, Medical University of Graz, Auenbruggerplatz 25, Graz A-8036, Austria. Johannes.haybaeck@medunigraz.at.
Medical University of Graz · ATThe University of Texas MD Anderson Cancer Center · USUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial carcinoma (EC), the second most common form of gynaecological malignancy, can be divided into two distinct sub-types: Type I tumours arise from hyperplastic endometrium and typically effect women around the time of menopause, whereas type II tumours arise in postmenopausal women from atrophic endometrium. Long non-coding RNAs (lncRNAs) are a novel class of non-protein coding molecules that have recently been implicated in the pathogenesis of many types of cancer including gynaecological tumours. Although they play critical physiological roles in cellular metabolism, their expression and function are deregulated in EC compared with paired normal tissue, indicating that they may also participate in tumour initiation and progression. For instance, the lncRNA MALAT-1 is down-regulated in EC samples compared to normal or hyperplastic endometrium, whereas the lncRNA OVAL is down-regulated in type II disease but up-regulated in type I disease. Other notatble lncRNAs such as HOTAIR, H19 and SRA become up-regulated with increasing EC tumour grade and other features associated with poor prognosis. In the current review, we will examine the growing body of evidence linking deregulated lncRNAs with specific biological functions of tumour cells in EC, we will highlight associations between lncRNAs and the molecular pathways implicated in EC tumourigenesis and we will identify critical knowledge gaps that remain to be addressed.

Indexed as

Gene Expression Regulation, NeoplasticEndometrial NeoplasmsFemaleHumansRNA, Long NoncodingRNA, Long Noncodingcancerendometrial carcinomalong non-coding RNAs

Identifiers

PMID26556343
PMCPMC4661821
OpenAlexW2109420358

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.