Evidence map›Paper›PMID 31958132›Full record

ArticleCarcinogenesis2020

RNA-binding protein CUGBP1 controls the differential INSR splicing in molecular subtypes of breast cancer cells and affects cell aggressiveness.

Gena Huang, Chen Song, Ning Wang, Tao Qin, Silei Sui, Alison Obr, Li Zeng, Teresa L Wood, Derek Leroith, Man Li and 1 more

Open access · greenAbstract read
In one paragraph

Article in Carcinogenesis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Gena HuangInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, Liaoning, China.
Chen SongDepartment of Breast Oncology, The Second Hospital of Dalian Medical University, Dalian, Liaoning, China.
Ning WangInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, Liaoning, China.
Tao QinDepartment of Pathology, Dalian Medical University, Dalian, Liaoning, China.
Silei SuiInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, Liaoning, China.
Alison ObrDepartment of Pharmacology, Physiology and Neuroscience, Rutgers New Jersey Medical School, Cancer Institute of New Jersey, Newark, NJ, USA.
Li ZengInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, Liaoning, China.
Teresa L WoodDepartment of Pharmacology, Physiology and Neuroscience, Rutgers New Jersey Medical School, Cancer Institute of New Jersey, Newark, NJ, USA.
Derek LeroithDivision of Endocrinology, Diabetes and Bone Disease, Department of Medicine, Icahn Mount Sinai School of Medicine, New York, NY, USA.
Man LiDepartment of Breast Oncology, The Second Hospital of Dalian Medical University, Dalian, Liaoning, China.
Yingjie WuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, Liaoning, China.
Dalian Medical University · CNRutgers, The State University of New Jersey · USIcahn School of Medicine at Mount Sinai · US

Funding

Mechanisms for the pro-metastatic effects of hyperinsulinemia on breast cancerR01CA128799 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LEROITH, DEREK · 2008 to 2018
$3.7M
Pathways that regulate basal and metastatic phenotypes in triple negative breast cancersR01CA204312 · NCI · RBHS-NEW JERSEY MEDICAL SCHOOL · PI WOOD, TERESA L · 2017 to 2021
$2.7M
NCI NIH HHS R01 CA128799NCI NIH HHS R01 CA204312
6 · The paper itself

Abstract

The insulin receptor gene (INSR) undergoes alternative splicing to give rise to two functionally related, but also distinct, isoforms IR-A and IR-B, which dictate proliferative and metabolic regulations, respectively. Previous studies identified the RNA-binding protein CUGBP1 as a key regulator of INSR splicing. In this study, we show that the differential splicing of INSR occurs more frequently in breast cancer than in non-tumor breast tissues. In breast cancer cell lines, the IR-A:IR-B ratio varies in different molecular subtypes, knockdown or overexpression of CUGBP1 gene in breast cancer cells altered IR-A:IR-B ratio through modulation of IR-A expression, thereby reversed or enhanced the insulin-induced oncogenic behavior of breast cancer cells, respectively. Our data revealed the predominant mitogenic role of IR-A isoform in breast cancer and depicted a novel interplay between INSR and CUGBP1, implicating CUGBP1 and IR-A isoform as the potential therapeutic targets and biomarkers for breast cancer.

Indexed as

RNA SplicingAntigens, CDBiomarkers, TumorBreast NeoplasmsCELF1 ProteinErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHumansPrognosisProtein IsoformsReceptor, InsulinReceptors, EstrogenReceptors, ProgesteroneAntigens, CDBiomarkers, TumorCELF1 ProteinCELF1 protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesINSR protein, humanProtein IsoformsReceptor, InsulinReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID31958132
PMCPMC7513956
OpenAlexW3002355040

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.