Evidence map›Paper›PMID 38879508›Full record

ArticleCell death & disease2024

Targeting LINC00152 activates cAMP/Ca

Ozge Saatci, Rashedul Alam, Kim-Tuyen Huynh-Dam, Aynur Isik, Meral Uner, Nevin Belder, Pelin Gulizar Ersan, Unal Metin Tokat, Burge Ulukan, Metin Cetin and 12 more

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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  15. HSPBiomedicines · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Ozge SaatciDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.ORCID 0000-0002-0124-044X
Rashedul AlamDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.
Kim-Tuyen Huynh-DamDepartment of Drug Discovery and Biomedical Sciences, University of South Carolina, Columbia, SC, 29208, USA.
Aynur IsikDepartment of Pathology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey.
Meral UnerDepartment of Pathology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey.ORCID 0000-0001-9927-1246
Nevin BelderDepartment of Molecular Biology and Genetics, Bilkent University, Ankara, 06800, Turkey.ORCID 0000-0001-9353-9387
Pelin Gulizar ErsanDepartment of Molecular Biology and Genetics, Bilkent University, Ankara, 06800, Turkey.ORCID 0000-0003-3637-4090
Unal Metin TokatDepartment of Molecular Biology and Genetics, Bilkent University, Ankara, 06800, Turkey.ORCID 0000-0003-0026-368X
Burge UlukanDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.ORCID 0000-0002-1101-8834
Metin CetinDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.
Kubra CalisirDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.ORCID 0000-0002-6204-1022
Mustafa Emre GedikDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.
Hilal BalDepartment of Molecular Biology and Genetics, Bilkent University, Ankara, 06800, Turkey.ORCID 0000-0003-1668-6070
Ozlem Sener SahinDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.
Yasser RiazalhosseiniDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Denis ThieffryDépartement de biologie de l'Ecole normale supérieure, PSL Université, 75005, Paris, France.
Daniel GautheretInstitute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CNRS, CEA, 91190, Gif-sur-Yvette, France.
Besim OgretmenDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA.ORCID 0000-0002-1019-5660
Sercan AksoyDepartment of Medical Oncology, Hacettepe University Cancer Institute, 06100, Ankara, Turkey.ORCID 0000-0003-4984-1049
Aysegul UnerDepartment of Pathology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey.
Aytekin AkyolDepartment of Pathology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey.
Ozgur SahinDepartment of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, 29425, USA. sahin@musc.edu.ORCID 0000-0002-8033-7089

Funding

RESEARCH PILOT PROJECTS PROGRAMP30GM103339 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HANNUN, YUSUF AWNI · 2012 to 2016
$5.4M
MUSC FACIL EXPANSION &RENOV: SLE C06RR015455 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND, JOHN R · 2002 to 2002
$2.0M
Overcoming chemoresistance in triple negative breast cancerR01CA267101 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI Ozgur Sahin · 2022 to 2026
$1.8M
Inhibiting tumor growth and metastasis in highly aggressive breast cancers with centrosome amplificationR01CA251374 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI SAHIN, OZGUR · 2021 to 2025
$1.7M
American Cancer Society (American Cancer Society, Inc.) RSG-19-194-01-CSMFoundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01CA251374Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01CA267101NCI NIH HHS R01 CA251374NCI NIH HHS R01 CA267101NCRR NIH HHS C06 RR015455NIGMS NIH HHS P30 GM103339Susan G. Komen (Susan G. Komen Breast Cancer Foundation) GTDR17500160
6 · The paper itself

Abstract

Tamoxifen has been the mainstay therapy to treat early, locally advanced, and metastatic estrogen receptor-positive (ER + ) breast cancer, constituting around 75% of all cases. However, the emergence of resistance is common, necessitating the identification of novel therapeutic targets. Here, we demonstrated that long-noncoding RNA LINC00152 confers tamoxifen resistance by blocking tamoxifen-induced ferroptosis, an iron-mediated cell death. Mechanistically, inhibiting LINC00152 reduces the mRNA stability of phosphodiesterase 4D (PDE4D), leading to activation of the cAMP/PKA/CREB axis and increased expression of the TRPC1 Ca

Indexed as

Breast NeoplasmsCalciumCyclic AMPDrug Resistance, NeoplasmFerroptosisRNA, Long NoncodingTamoxifenAnimalsCell Line, TumorFemaleHumansMCF-7 CellsMiceReactive Oxygen SpeciesReceptors, EstrogenCalciumCyclic AMPReactive Oxygen SpeciesReceptors, EstrogenRNA, Long NoncodingTamoxifen

Identifiers

PMID38879508
PMCPMC11180193

What OpenQuestion 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 OpenQuestion graph.