Evidence map›Paper›PMID 39335212›Full record

ArticleCancers2024

Induction of Invasive Basal Phenotype in Triple-Negative Breast Cancers by Long Noncoding RNA BORG.

Farshad Niazi, Kimberly A Parker, Sara J Mason, Salendra Singh, William P Schiemann, Saba Valadkhan

Abstract read
In one paragraph

Article in Cancers, 2024. 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

6 authors.

Farshad NiaziDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH 44106, USA.
Kimberly A ParkerDepartment of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Sara J MasonDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH 44106, USA.
Salendra SinghCenter for Immunotherapy and Precision Immuno-Oncology (CITI), Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.ORCID 0000-0002-4903-9868
William P SchiemannDepartment of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Saba ValadkhanDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH 44106, USA.

Funding

PREDOCTORAL TRAINING PROGRAM IN MOLECULAR THERAPEUTICST32GM008803 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI MIEYAL, JOHN J, NIEMAN, MARVIN THOMAS · 2001 to 2023
$4.2M
Role of the lncRNA BORG in Breast Cancer Metastatic Progression and RecurrenceR01CA236273 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI SCHIEMANN, WILLIAM, VALADKHAN, SABA · 2019 to 2023
$2.3M
Case Comprehensive Cancer Center NoneNIGMS NIH HHS T32 GM008803NIH HHS 1R01CA236273-05A1
6 · The paper itself

Abstract

BACKGROUND/

objectivesLong noncoding RNAs (lncRNAs) are known to play key roles in breast cancers; however, detailed mechanistic studies of lncRNA function have not been conducted in large cohorts of breast cancer tumors, nor has inter-donor and inter-subtype variability been taken into consideration for these analyses. Here we provide the first identification and annotation of the human BORG lncRNA gene. METHODS/

resultsUsing multiple tumor cohorts of human breast cancers, we show that while BORG expression is strongly induced in breast tumors as compared to normal breast tissues, the extent of BORG induction varies widely between breast cancer subtypes and even between different tumors within the same subtype. Elevated levels of BORG in breast tumors are associated with the acquisition of core cancer aggression pathways, including those associated with basal tumor and pluripotency phenotypes and with epithelial-mesenchymal transition (EMT) programs. While a subset of BORG-associated pathways was present in high BORG-expressing tumors across all breast cancer subtypes, many were specific to tumors categorized as triple-negative breast cancers. Finally, we show that genes induced by heterologous expression of BORG in murine models of TNBC both in vitro and in vivo strongly overlap with those associated with high BORG expression levels in human TNBC tumors.

conclusionOur findings implicate human BORG as a novel driver of the highly aggressive basal TNBC tumor phenotype.

Indexed as

BORGcancer stem cellslncRNAsTNBC

Identifiers

PMID39335212
PMCPMC11430157

What Socratic holds

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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 Socratic graph.