Evidence map›Paper›PMID 29547122›Full record

ArticleeLife2018

SPIN1 promotes tumorigenesis by blocking the uL18 (universal large ribosomal subunit protein 18)-MDM2-p53 pathway in human cancer.

Ziling Fang, Bo Cao, Jun-Ming Liao, Jun Deng, Kevin D Plummer, Peng Liao, Tao Liu, Wensheng Zhang, Kun Zhang, Li Li and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
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  11. Epigenetic Regulation Via Electrical Forces.Reviews of physiology, biochemistry and pharmacology · 2025
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  15. Article
  16. RNA-binding motif protein 10 inactivates c-Myc by partnering with ribosomal proteins uL18 and uL5.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. 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

14 authors at 4 institutions in 2 countries.

Ziling FangDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Bo CaoDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Jun-Ming LiaoDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Jun DengDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Kevin D PlummerDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Peng LiaoDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Tao LiuDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Wensheng ZhangDepartment of Computer Science, Bioinformatics Facility of Xavier RCMI Center of Cancer Research, Xavier University of Louisiana, New Orleans, United States.
Kun ZhangDepartment of Computer Science, Bioinformatics Facility of Xavier RCMI Center of Cancer Research, Xavier University of Louisiana, New Orleans, United States.
Li LiLaboratory of Translational Cancer Research, Ochsner Clinical Foundation, New Orleans, United States.
David MargolinDepartment of Colon and Rectal Surgery, Ochsner Clinical Foundation, New Orleans, United States.
Shelya X ZengDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
Jianping XiongDepartment of Oncology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Hua LuDepartment of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.ORCID http://orcid.org/0000-0002-9285-7209
Tulane University · USOchsner Medical Center · USXavier University of Louisiana · USNanchang University · CN

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Xavier's RCMI Cancer Research ProgramG12MD007595 · NIMHD · XAVIER UNIVERSITY OF LOUISIANA · PI D'AMOUR, GENE, WANG, GUANGDI · 2012 to 2018
$15.7M
The Role of Ribosomal Proteins in the P53-MDM2 PathwayR01CA095441 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI LU, HUA · 2002 to 2021
$5.1M
Role of the AMPK-MDMX-p53 pathway in cancerR01CA127724 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI LU, HUA · 2007 to 2019
$3.0M
Dual Targeting of the p53 pathway for development of anti-cancer therapyR01CA172468 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI LU, HUA · 2012 to 2016
$1.5M
Role of TFIIS.h in regulation of p53 responsive apoptosis and tumor suppressionR21CA201889 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI LU, HUA · 2016 to 2017
$360k
Targeting GRP78 for p53 activation as anti-cancer therapyR21CA190775 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI LU, HUA · 2015 to 2016
$360k
NCI NIH HHS R01 CA095441NCI NIH HHS R01 CA127724NCI NIH HHS R01 CA172468NCI NIH HHS R21 CA190775NCI NIH HHS R21 CA201889NIGMS NIH HHS U54 GM104940NIH HHS 2G12MD007595NIH HHS R01CA095441NIH HHS R01CA127724NIH HHS R01CA172468NIH HHS R21CA190775NIH HHS R21 CA201889NIMHD NIH HHS G12 MD007595
6 · The paper itself

Abstract

Ribosomal proteins (RPs) play important roles in modulating the MDM2-p53 pathway. However, less is known about the upstream regulators of the RPs. Here, we identify SPIN1 (Spindlin 1) as a novel binding partner of human RPL5/uL18 that is important for this pathway. SPIN1 ablation activates p53, suppresses cell growth, reduces clonogenic ability, and induces apoptosis of human cancer cells. Mechanistically, SPIN1 sequesters uL18 in the nucleolus, preventing it from interacting with MDM2, and thereby alleviating uL18-mediated inhibition of MDM2 ubiquitin ligase activity toward p53. SPIN1 deficiency increases ribosome-free uL18 and uL5 (human RPL11), which are required for SPIN1 depletion-induced p53 activation. Analysis of cancer genomic databases suggests that SPIN1 is highly expressed in several human cancers, and its overexpression is positively correlated with poor prognosis in cancer patients. Altogether, our findings reveal that the oncogenic property of SPIN1 may be attributed to its negative regulation of uL18, leading to p53 inactivation.

Indexed as

AnimalsCarcinogenesisCell Cycle ProteinsCell Line, TumorCell ProliferationCells, CulturedGene Expression Regulation, NeoplasticHCT116 CellsHEK293 CellsHumansMiceMicrotubule-Associated ProteinsNeoplasmsPhosphoproteinsProto-Oncogene Proteins c-mdm2Ribosomal ProteinsCell Cycle ProteinsMicrotubule-Associated ProteinsPhosphoproteinsProto-Oncogene Proteins c-mdm2Ribosomal ProteinsspindlinTumor Suppressor Protein p53cancer biologycancer cell survivalhumanMDM2p53RPL5/uL18SPIN1tumorigenesis

Identifiers

PMID29547122
PMCPMC5871334
OpenAlexW2789580736

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.