Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/8229
Title: Expression Profiles and Biomarker Potential of Long Non-Coding RNAs H19, NEAT1, MALAT1 and HOTAIR in Locally Advanced Rectal Cancer Patients
Authors: Erić, K.
Rosić Stojković, J.
Miladinov, M.
Dragičević, S.
Barišić, G.
Marković, V.
Zeljić, Katarina 
Keywords: Rectal cancer;;H19;;NEAT1;;MALAT1;;HOTAIR;;Neoadjuvant chemoradiotherapy.
Issue Date: 9-Feb-2026
Rank: M21
Publisher: MDPI
Journal: International Journal of Molecular Sciences
Volume: 27
Issue: 4
Start page: 1672
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.
URI: https://biore.bio.bg.ac.rs/handle/123456789/8229
DOI: 10.3390/ijms27041672
Appears in Collections:Journal Article

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