Evidence map›Paper›PMID 27462423›Full record

ArticleCell discovery2015

A novel ER-microtubule-binding protein, ERLIN2, stabilizes Cyclin B1 and regulates cell cycle progression.

Xuebao Zhang, Juan Cai, Ze Zheng, Lisa Polin, Zhenghong Lin, Aditya Dandekar, Li Li, Fei Sun, Russell L Finley, Deyu Fang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell discovery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  18. Cell cycle (Georgetown, Tex.) · 2019
    Article
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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

12 authors at 3 institutions in 1 country.

Xuebao ZhangCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine , Detroit, MI, USA.
Juan CaiCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine , Detroit, MI, USA.
Ze ZhengCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine , Detroit, MI, USA.
Lisa PolinKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA; Department of Oncology, Wayne State University School of Medicine, Detroit, MI, USA.
Zhenghong LinDepartment of Pathology, Northwestern University Feinberg School of Medicine , Chicago, IL, USA.
Aditya DandekarDepartment of Immunology and Microbiology, Wayne State University School of Medicine , Detroit, MI, USA.
Li LiCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, USA; Department of Internal Medicine, Wayne State University School of Medicine, Detroit, MI, USA.
Fei SunDepartment of Physiology, Wayne State University School of Medicine , Chicago, IL, USA.
Russell L FinleyCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, USA; Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA; Department of Biochemistry and Molecular Biology, Wayne State University School of Medicine, Detroit, MI, USA.
Deyu FangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Zeng-Quan YangKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA; Department of Oncology, Wayne State University School of Medicine, Detroit, MI, USA.
Kezhong ZhangCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, USA; Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA; Department of Immunology and Microbiology, Wayne State University School of Medicine, Detroit, MI, USA.
Wayne State University · USNorthwestern University · USThe Barbara Ann Karmanos Cancer Institute · US

Funding

Regulation of Hepatic Steatosis by an ER Stress-Inducible Transcription Factor CRR01DK090313 · NIDDK · WAYNE STATE UNIVERSITY · PI Kezhong Zhang · 2011 to 2026
$5.0M
Simultaneous Targeting of IRE1a in B Cells and Macrophages for Lupus TherapyR01AR066634 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FANG, DEYU, ZHANG, KEZHONG · 2014 to 2018
$1.7M
Airborne Particulate Matter, Endoplasmic Reticulum Stress and Hepatic Lipid DysreR21ES017829 · NIEHS · WAYNE STATE UNIVERSITY · PI ZHANG, KEZHONG · 2010 to 2011
$442k
NIAMS NIH HHS R01 AR066634NIDDK NIH HHS R01 DK090313NIEHS NIH HHS R21 ES017829
6 · The paper itself

Abstract

The gene encoding endoplasmic reticulum (ER) lipid raft-associated protein 2 (ERLIN2) is amplified in human breast cancers. ERLIN2 gene mutations were also found to be associated with human childhood progressive motor neuron diseases. Yet, an understanding of the physiological function and mechanism for ERLIN2 remains elusive. In this study, we reveal that ERLIN2 is a spatially and temporally regulated ER-microtubule-binding protein that has an important role in cell cycle progression by interacting with and stabilizing the mitosis-promoting factors. Whereas ERLIN2 is highly expressed in aggressive human breast cancers, during normal development ERLIN2 is expressed at the postnatal stage and becomes undetectable in adulthood. ERLIN2 interacts with the microtubule component α-tubulin, and this interaction is maximal during the cell cycle G2/M phase where ERLIN2 simultaneously interacts with the mitosis-promoting complex Cyclin B1/Cdk1. ERLIN2 facilitates K63-linked ubiquitination and stabilization of Cyclin B1 protein in G2/M phase. Downregulation of ERLIN2 results in cell cycle arrest, represses breast cancer proliferation and malignancy and increases sensitivity of breast cancer cells to anticancer drugs. In summary, our study revealed a novel ER-microtubule-binding protein, ERLIN2, which interacts with and stabilizes mitosis-promoting factors to regulate cell cycle progression associated with human breast cancer malignancy.

Indexed as

breast cancerCyclin B1endoplasmic reticulumER lipid raft proteinmicrotubulemitosis

Identifiers

PMID27462423
PMCPMC4860859
OpenAlexW2520630049

What OpenQuestion 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 OpenQuestion graph.