Evidence map›Paper›PMID 37502925›Full record

ArticleResearch square2023

Protein arginine methyltransferase 5 (PRMT5) is an actionable therapeutic target in CDK4/6 inhibitor-resistant ER+/RB-deficient breast cancer.

Chang-Ching Lin, Tsung-Cheng Chang, Yunguan Wang, Lei Guo, Yunpeng Gao, Emmanuel Bikorimana, Andrew Lemoff, Yisheng V Fang, He Zhang, Yanfeng Zhang and 15 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. 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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 6 institutions in 5 countries.

Chang-Ching LinHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Tsung-Cheng ChangDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.
Yunguan WangQuantitative Biomedical Research Center, Department of Population & Data Sciences, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Lei GuoQuantitative Biomedical Research Center, Department of Population & Data Sciences, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Yunpeng GaoDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, USA.
Emmanuel BikorimanaHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Andrew LemoffDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
Yisheng V FangHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
He ZhangQuantitative Biomedical Research Center, Department of Population & Data Sciences, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Yanfeng ZhangQuantitative Biomedical Research Center, Department of Population & Data Sciences, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Dan YeHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Isabel Soria-BretonesPrincess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
Alberto ServettoHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Kyung-Min LeeHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-8381-2423
Xuemei LuoDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
Joseph J OttoDepartment of Biochemistry, UT Southwestern Medical Center, Dallas, TX, USA.
Hiroaki AkamatsuHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Fabiana NapolitanoHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Ram ManiDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-3552-7905
David W CesconPrincess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-1080-0998
Lin XuQuantitative Biomedical Research Center, Department of Population & Data Sciences, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-5815-4457
Yang XieQuantitative Biomedical Research Center, Department of Population & Data Sciences, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Joshua T MendellDepartment of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-8479-2284
Ariella B HankerHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-8655-8341
Carlos L ArteagaHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-0870-9586
Southwestern Medical Center · USThe University of Texas Southwestern Medical Center · USHoward Hughes Medical Institute · USUniversity Health Network · CASouthwestern Medical CenterWakayama Medical University · JP

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
Role of HER2 mutations in breast cancer progression and response to targeted therapiesR01CA224899 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI ARTEAGA, CARLOS L · 2018 to 2022
$1.8M
NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA098131NCI NIH HHS R01 CA224899
6 · The paper itself

Abstract

CDK4/6 inhibitors (CDK4/6i) have improved survival of patients with estrogen receptor-positive (ER+) breast cancer. However, patients treated with CDK4/6i eventually develop drug resistance and progress.

Identifiers

PMID37502925
PMCPMC10371097
OpenAlexW4383750469

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.