Evidence map›Paper›PMID 37795578›Full record

ReviewCancer medicine2023

Roles of long noncoding RNA in triple-negative breast cancer.

Plabon Kumar Das, Ayesha Siddika, Khan Mohammad Rashel, Abdul Auwal, Kazi Soha, Md Arifur Rahman, Suja Pillai, Farhadul Islam

Open access · goldAbstract readReview
In one paragraph

Review in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

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  5. Molecular Effects of Glucose onBritish journal of biomedical science · 2025
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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

8 authors at 4 institutions in 2 countries.

Plabon Kumar DasDepartment of Biochemistry & Molecular Biology, Rajshahi University, Rajshahi, Bangladesh.
Ayesha SiddikaInstitute of Tissue Banking & Biomaterial Research, Atomic Energy Research Establishment (AERE) Savar, Dhaka, Bangladesh.
Khan Mohammad RashelDepartment of Biochemistry & Molecular Biology, Rajshahi University, Rajshahi, Bangladesh.
Abdul AuwalDepartment of Biochemistry & Molecular Biology, Rajshahi University, Rajshahi, Bangladesh.
Kazi SohaDepartment of Biochemistry & Molecular Biology, Rajshahi University, Rajshahi, Bangladesh.
Md Arifur RahmanDepartment of Biochemistry & Molecular Biology, Rajshahi University, Rajshahi, Bangladesh.
Suja PillaiSchool of Biomedical Sciences, University of Queensland, Saint Lucia, Australia.
Farhadul IslamDepartment of Biochemistry & Molecular Biology, Rajshahi University, Rajshahi, Bangladesh.ORCID 0000-0001-5262-4702
University of Rajshahi · BDGriffith University · AUBangladesh Atomic Energy Commission · BDThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLong noncoding RNAs (lncRNAs) play crucial roles in regulating various hallmarks in cancers. Triple-negative (Estrogen receptor, ER; Human epidermal growth factor receptor 2, HER2; Progesterone receptor, PR) breast cancer (TNBC) is the most aggressive form of breast cancers with a poor prognosis and no available molecular targeted therapy.

methodsWe reviewed the current literature on the roles of lncRNAs in the pathogenesis, therapy resistance, and prognosis of patients with TBNC.

resultsLncRNAs are associated with TNBC pathogenesis, therapy resistance, and prognosis. For example, lncRNAs such as small nucleolar RNA host gene 12 (SNHG12), highly upregulated in liver cancer (HULC) HOX transcript antisense intergenic RNA (HOTAIR), lincRNA-regulator of reprogramming (LincRNA-ROR), etc., are aberrantly expressed in TNBC and are involved in the pathogenesis of the disease. LncRNAs act as a decoy, scaffold, or sponge to regulate the expression of genes, miRNAs, and transcription factors associated with pathogenesis and progression of TNBC. Moreover, lncRNAs such as ferritin heavy chain 1 pseudogene 3 (FTH1P3), BMP/OP-responsive gene (BORG) contributes to the therapy resistance property of TNBC through activating ABCB1 (ATP-binding cassette subfamily B member 1) drug efflux pumps by increasing DNA repair capacity or by inducing signaling pathway involved in therapeutic resistance.

conclusionIn this review, we outline the functions of various lncRNAs along with their molecular mechanisms involved in the pathogenesis, therapeutic resistance of TBNC. Also, the prognostic implications of lncRNAs in patients with TNBC is illustrated. Moreover, potential strategies targeting lncRNAs against highly aggressive TNBC is discussed in this review.

Indexed as

MicroRNAsRNA, Long NoncodingTriple Negative Breast NeoplasmsGene Expression Regulation, NeoplasticHumansPrognosisMicroRNAsRNA, Long Noncodingchemotherapy resistancelong noncoding RNAspathogenesisprognosisradiotherapy resistancetargeted therapies

Identifiers

PMID37795578
PMCPMC10652353
OpenAlexW4387356875

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.