Evidence map›Paper›PMID 24656772›Full record

ArticleCancer cell2014

SPOP promotes tumorigenesis by acting as a key regulatory hub in kidney cancer.

Guoqiang Li, Weimin Ci, Subhradip Karmakar, Ke Chen, Ruby Dhar, Zhixiang Fan, Zhongqiang Guo, Jing Zhang, Yuwen Ke, Lu Wang and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

112 citing papers in PubMed, 1 synthesis or guideline pooled it, 176 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. High-throughput screening identifies a critical role of the SPOP-PABPC1 axis in lung adenocarcinoma progression.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Molecular insights for the tumor suppressor role of SPOP in prostate cancer.Biochimica et biophysica acta. Reviews on cancer · 2026
    Review
  7. Article
  8. NUSAP1 Recruits DAXX to Suppress HIF-Driven Triple-Negative Breast Cancer Progression.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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  19. Article
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52 more citing papers are in PubMed but not listed here.

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

25 authors at 10 institutions in 2 countries.

Guoqiang LiKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Weimin CiLaboratory of Disease Genomics and Individualized Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
Subhradip KarmakarInstitute for Genomics and Systems Biology, University of Chicago and Argonne National Laboratory, Chicago, IL 60637, USA; Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Ke ChenKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
Ruby DharInstitute for Genomics and Systems Biology, University of Chicago and Argonne National Laboratory, Chicago, IL 60637, USA; Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Zhixiang FanKunming Medical University, Kunming, Yunnan 650500, China.
Zhongqiang GuoKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China; Department of Urology, First Hospital of Peking University, Beijing 100034, China.
Jing ZhangKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
Yuwen KeKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
Lu WangKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Min ZhuangDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA 94158, USA.
Shengdi HuLaboratory of Animal Research Center, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.
Xuesong LiDepartment of Urology, First Hospital of Peking University, Beijing 100034, China.
Liqun ZhouDepartment of Urology, First Hospital of Peking University, Beijing 100034, China.
Xianghong LiDepartment of Pathology, Peking University Cancer Hospital, Beijing 100142, China.
Matthew F CalabreseDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Edmond R WatsonDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Sandip M PrasadSection of Urology, Department of Surgery, University of Chicago, Chicago, IL 60637, USA.
Carrie Rinker-SchaefferSection of Urology, Department of Surgery, University of Chicago, Chicago, IL 60637, USA.
Scott E EggenerSection of Urology, Department of Surgery, University of Chicago, Chicago, IL 60637, USA.
Thomas StrickerInstitute for Genomics and Systems Biology, University of Chicago and Argonne National Laboratory, Chicago, IL 60637, USA; Department of Pathology, University of Chicago, Chicago, IL 60637, USA.
Yong TianLaboratory of Animal Research Center, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.
Brenda A SchulmanDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA; Howard Hughes Medical Institute, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Jiang LiuKey Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China. Electronic address: liuj@big.ac.cn.
Kevin P WhiteInstitute for Genomics and Systems Biology, University of Chicago and Argonne National Laboratory, Chicago, IL 60637, USA; Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA; Section on Genetic Medicine, Department of Medicine, University of Chicago, Chicago, IL 60637, USA. Electronic address: kpwhite@uchicago.edu.
Beijing Institute of Genomics · CNChinese Academy of Sciences · CNUniversity of Chicago · USArgonne National Laboratory · USSt. Jude Children's Research Hospital · USInstitute of Biophysics · CNPeking University Cancer Hospital · CNKunming Medical University · CNPeking University · CNUniversity of California, San Francisco · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
CORE: ADMINISTRATIVEP50GM081892 · NIGMS · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2008 to 2013
$15.9M
Ubiquitin-like Protein Transfer CascadesR01GM069530 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SCHULMAN, BRENDA A · 2003 to 2013
$3.4M
The Role of Brain Stress Systems in the Prefrontal Cortex in Compulsive DrinkingR01AA020608 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI GEORGE, OLIVIER · 2011 to 2015
$1.8M
Howard Hughes Medical InstituteNCI NIH HHS 5P30CA021765NCI NIH HHS P30 CA021765NIAAA NIH HHS R01 AA020608NIGMS NIH HHS 5R01GM069530NIGMS NIH HHS P50 GM081892NIGMS NIH HHS P50GM081892NIGMS NIH HHS R01 GM069530NIGMS NIH HHS T32 GM007281
6 · The paper itself

Abstract

Hypoxic stress and hypoxia-inducible factors (HIFs) play important roles in a wide range of tumors. We demonstrate that SPOP, which encodes an E3 ubiquitin ligase component, is a direct transcriptional target of HIFs in clear cell renal cell carcinoma (ccRCC). Furthermore, hypoxia results in cytoplasmic accumulation of SPOP, which is sufficient to induce tumorigenesis. This tumorigenic activity occurs through the ubiquitination and degradation of multiple regulators of cellular proliferation and apoptosis, including the tumor suppressor PTEN, ERK phosphatases, the proapoptotic molecule Daxx, and the Hedgehog pathway transcription factor Gli2. Knockdown of SPOP specifically kills ccRCC cells, indicating that it may be a promising therapeutic target. Collectively, our results indicate that SPOP serves as a regulatory hub to promote ccRCC tumorigenesis.

Indexed as

AnimalsCarcinogenesisCarcinoma, Renal CellCell Transformation, NeoplasticGene Knockdown TechniquesHEK293 CellsHeterograftsHumansKidney NeoplasmsMiceMice, Inbred BALB CMice, NudeNuclear ProteinsRepressor ProteinsSignal TransductionUbiquitinationNuclear ProteinsRepressor ProteinsSPOP protein, humanUbiquitin-Protein Ligases

Identifiers

PMID24656772
PMCPMC4443692
OpenAlexW2061358469

What OpenQuestion holds

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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.