Evidence map›Paper›PMID 24768297›Full record

ArticleCell metabolism2014

PTENα, a PTEN isoform translated through alternative initiation, regulates mitochondrial function and energy metabolism.

Hui Liang, Shiming He, Jingyi Yang, Xinying Jia, Pan Wang, Xi Chen, Zhong Zhang, Xiajuan Zou, Michael A McNutt, Wen Hong Shen and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed
10.2field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 236 citations in OpenAlex.

  1. Article
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  8. Review
  9. LncPTEN1, a long non-coding RNA generated fromNon-coding RNA research · 2025
    Article
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  17. PTEN: a new dawn in Parkinson's disease treatment.Frontiers in cellular neuroscience · 2025
    Review
  18. Article
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  20. Article

81 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Hui LiangInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Shiming HeInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Jingyi YangInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Xinying JiaInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China; Department of Radiation Oncology, Weill Medical College of Cornell University, New York, NY 10065, USA.
Pan WangInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Xi ChenInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Zhong ZhangInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China; Department of Radiation Oncology, Weill Medical College of Cornell University, New York, NY 10065, USA.
Xiajuan ZouInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Michael A McNuttInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China.
Wen Hong ShenDepartment of Radiation Oncology, Weill Medical College of Cornell University, New York, NY 10065, USA. Electronic address: wes2007@med.cornell.edu.
Yuxin YinInstitute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Center for Age-Related Diseases, Peking University Health Science Center, Beijing 100191, P.R. China. Electronic address: yinyuxin@hsc.pku.edu.cn.
Peking University · CNCornell University · US

Funding

Role of PTEN in Mitosis and Chromosome StabilityR01GM100478 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SHEN, WEN H. · 2012 to 2020
$2.9M
PTEN Deficiency and Tumor DevelopmentR01CA133008 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI YIN, YUXIN · 2009 to 2012
$1.4M
NCI NIH HHS R01 CA133008NCI NIH HHS R01CA133008NIGMS NIH HHS R01 GM100478NIGMS NIH HHS R01GM100478
6 · The paper itself

Abstract

PTEN is one of the most frequently mutated genes in human cancer. It is known that PTEN has a wide range of biological functions beyond tumor suppression. Here, we report that PTENα, an N-terminally extended form of PTEN, functions in mitochondrial metabolism. Translation of PTENα is initiated from a CUG codon upstream of and in-frame with the coding region of canonical PTEN. Eukaryotic translation initiation factor 2A (eIF2A) controls PTENα translation, which requires a CUG-centered palindromic motif. We show that PTENα induces cytochrome c oxidase activity and ATP production in mitochondria. TALEN-mediated somatic deletion of PTENα impairs mitochondrial respiratory chain function. PTENα interacts with canonical PTEN to increase PINK1 protein levels and promote energy production. Our studies demonstrate the importance of eIF2A-mediated alternative translation for generation of protein diversity in eukaryotic systems and provide insights into the mechanism by which the PTEN family is involved in multiple cellular processes.

Indexed as

Adenosine TriphosphateAmino Acid SequenceAnimalsBase SequenceElectron TransportElectron Transport Complex IVEnergy MetabolismMiceMitochondriaMolecular Sequence DataProtein BiosynthesisProtein IsoformsProtein KinasesPTEN-Induced Putative KinasePTEN PhosphohydrolaseAdenosine TriphosphateElectron Transport Complex IVProtein IsoformsProtein KinasesPTEN-Induced Putative KinasePTEN PhosphohydrolasePten protein, mouse

Identifiers

PMID24768297
PMCPMC4097321
OpenAlexW2085377666

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.