Evidence map›Paper›PMID 41751809›Full record

ArticleInternational journal of molecular sciences2026

Expression Profiles and Biomarker Potential of Long Non-Coding RNAs H19, NEAT1, MALAT1 and HOTAIR in Locally Advanced Rectal Cancer Patients.

Katarina Eric, Jovana Rosic Stojkovic, Marko Miladinov, Sandra Dragicevic, Goran Barisic, Velimir Markovic, Katarina Zeljic

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. 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
–field-weighted citation impact
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.

  1. Biology · 2026
    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

7 authors.

Katarina EricDepartment of Pathology, Pathohistology and Medical Cytology, University Clinical Center of Serbia, 11000 Belgrade, Serbia.ORCID 0009-0003-9101-5979
Jovana Rosic StojkovicFaculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0001-6557-0010
Marko MiladinovClinic for Digestive Surgery-First Surgical Clinic, University Clinical Center of Serbia, 11000 Belgrade, Serbia.
Sandra DragicevicGene Regulation in Cancer Group, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-1602-1880
Goran BarisicFaculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Velimir MarkovicFaculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Katarina ZeljicFaculty of Biology, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-6545-8616

Funding

Ministry of Science, Technological development and Innovations of the Republic of Serbia 451-03-137/2025-03/200178, 451-03-137/2025-03/200110 and 451-03-136/2025-03/200042Serbian Academy of Sciences and Arts F-69 (grant agreement No 02-2019)
6 · The paper itself

Abstract

Locally advanced rectal cancer (LARC) presents a clinical challenge due to lack of reliable molecular biomarkers for early diagnosis, prognosis, and prediction of response to neoadjuvant chemoradiotherapy (nCRT). Long non-coding RNAs (lncRNAs) have emerged as promising candidates due to their characteristics and regulatory roles. H19, NEAT1, MALAT1 and HOTAIR are lncRNAs deregulated in gastrointestinal cancers, with insufficient data on their biomarker potential in LARC. The study aimed to analyze the diagnostic, prognostic and predictive utility of H19, NEAT1, MALAT1 and HOTAIR in LARC. Relative expression was evaluated by RT-qPCR in tumor and non-tumor tissues from 25 LARC patients before and after nCRT. H19, NEAT1, and MALAT1 showed significantly altered expression in tumor tissue, as well as non-tumor tissue before and after nCRT. H19 expression was significantly higher in tumor vs. non-tumor tissue before treatment and demonstrated moderate potential to discriminate between tumor and non-tumor. None of the lncRNAs showed statistically significant predictive values for nCRT response or association with treatment outcomes in our study, which was limited by the small number of responders. Our results suggest that H19 might be considered as a potential therapeutic target in LARC. Further studies with larger patient groups are required to confirm its diagnostic and prognostic utility.

Indexed as

Biomarkers, TumorRectal NeoplasmsRNA, Long NoncodingAdultAgedFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoadjuvant TherapyPrognosisBiomarkers, TumorH19 long non-coding RNAHOTAIR long untranslated RNA, humanMALAT1 long non-coding RNA, humanNEAT1 long non-coding RNA, humanRNA, Long NoncodingH19HOTAIRMALAT1NEAT1neoadjuvant chemoradiotherapyrectal cancer

Identifiers

PMID41751809
PMCPMC12940164

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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.