Evidence map›Paper›PMID 41139763›Full record

ReviewJournal of the Egyptian National Cancer Institute2025

Unraveling LncRNAs: the future of lung cancer treatment.

Zahraa Isam Jameel, Halla Abdul-Hadi Chabuk

Abstract readReview
In one paragraph

Review in Journal of the Egyptian National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

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

2 authors.

Zahraa Isam JameelDepartment of Biology, College of Science, Al-Qasim Green University, Al‑Qasim, Babil, Iraq. zahraa.isam@science.uoqasim.edu.iq.
Halla Abdul-Hadi ChabukDepartment of Biology, College of Science, University of Babylon, Babil, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding ribonucleic acids (LncRNAs) are larger than 200 nucleotides and resemble messenger ribonucleic acids (mRNAs), but they do not code for proteins. In both cell development and physiological cell function, LncRNAs have crucial biological functions. Consequently, cancer entails the disruption of their biological function. Many people die from lung cancer because it is diagnosed late, spreads to other parts of the body, and has a high treatment failure rate. Because they can be involved in either oncogenic or tumor-suppressing functions, LncRNAs are quickly becoming core molecules in lung cancer. Since LncRNAs are long-lasting in blood, they can be utilized as non-invasive diagnostic tools for cancer at an early stage. We review the latest research that has brought together evidence from real-world observations concerning the processes through which LncRNAs work in cancer formation, how they allow cancer to develop drug resistance, and how they can be used as possible diagnostic tools and markers of outcome, with a focus on lung cancer. We also cover some of the ongoing treatment strategies that can target LncRNAs. As seen from what has been laid out here, the examination of LncRNAs in lung cancer with protein-coding genes could provide evidence for a further elucidation of the molecular events behind the disease as well as its progression, and the potential for a new therapeutic pathway.

Indexed as

Biomarkers, TumorLung NeoplasmsRNA, Long NoncodingDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansBiomarkers, TumorRNA, Long NoncodingBiomarkerDysregulationLncRNAsLung cancerMetastasis

Identifiers

PMID41139763
PMCPMC13313518

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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.