Evidence map›Paper›PMID 25378405›Full record

ArticleThe Journal of biological chemistry2014

Sestrin2 protein positively regulates AKT enzyme signaling and survival in human squamous cell carcinoma and melanoma cells.

Baozhong Zhao, Palak Shah, Andrei V Budanov, Lei Qiang, Mei Ming, Andrew Aplin, Diane M Sims, Yu-Ying He

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
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  7. Review
  8. Genes · 2023
    Article
  9. Article
  10. Article
  11. The functions and roles of sestrins in regulating human diseases.Cellular & molecular biology letters · 2022
    Review
  12. Calycosin induces autophagy and apoptosisFrontiers in pharmacology · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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

8 authors at 3 institutions in 1 country.

Baozhong ZhaoFrom the Department of Medicine, Section of Dermatology, University of Chicago, Chicago, Illinois 60637.
Palak ShahFrom the Department of Medicine, Section of Dermatology, University of Chicago, Chicago, Illinois 60637.
Andrei V BudanovDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, Virginia 23298.
Lei QiangFrom the Department of Medicine, Section of Dermatology, University of Chicago, Chicago, Illinois 60637.
Mei MingFrom the Department of Medicine, Section of Dermatology, University of Chicago, Chicago, Illinois 60637.
Andrew AplinDepartment of Cancer Biology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, and Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Diane M SimsFrom the Department of Medicine, Section of Dermatology, University of Chicago, Chicago, Illinois 60637.
Yu-Ying HeFrom the Department of Medicine, Section of Dermatology, University of Chicago, Chicago, Illinois 60637, yyhe@medicine.bsd.uchicago.edu.
University of Chicago · USThomas Jefferson University · USVirginia Commonwealth University · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Mechanisms of UVA-induced skin cancerR01ES016936 · NIEHS · UNIVERSITY OF CHICAGO · PI HE, YU-YING · 2010 to 2014
$2.2M
The Role of p53-inducible Sesn1 and Sesn2 genes in lung carcinogenesisR01CA172660 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI GROSSMAN, STEVEN R. · 2013 to 2017
$1.5M
NCATS NIH HHS UL1 TR000430NCI NIH HHS CA172660NCI NIH HHS P30 CA014599NCI NIH HHS R01 CA172660NIEHS NIH HHS ES016936NIEHS NIH HHS R01 ES016936NIGMS NIH HHS GM067983
6 · The paper itself

Abstract

Skin cancer is the most common cancer in the United States and is mainly caused by environmental UV radiation. Reducing skin cancer incidence is becoming an urgent issue. The stress-inducible protein Sestrin2 (Sesn2) plays an important role in maintaining redox and metabolic homeostasis and their related pathologies. However, the role of Sesn2 in cancer remains unclear. Here we show that UVB radiation induces Sesn2 expression in normal human keratinocytes, mouse skin, normal human melanocytes, and melanoma cells. In addition, Sesn2 promotes AKT activation through a PTEN-dependent mechanism. Sesn2 deletion or knockdown sensitizes squamous cell carcinoma (SCC) cells to 5-fluorouracil-induced apoptosis and melanoma cells to UVB- and vemurafenib-induced apoptosis. In mice Sesn2 knockdown suppresses tumor growth from injected human SCC and melanoma cells. Last, as compared with normal skin, Sesn2 is up-regulated in both human skin SCC and melanoma. Our findings demonstrate that Sesn2 promotes AKT activation and survival in response to UVB stress and chemotherapeutics and suggest that Sesn2 is oncogenic in skin SCC and melanoma.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinoma, Squamous CellCell SurvivalFemaleHeLa CellsHumansMelanoma, ExperimentalMiceMice, NudeNeoplasm TransplantationNuclear ProteinsProto-Oncogene Proteins c-aktSestrinsSignal TransductionAntineoplastic AgentsNuclear ProteinsProto-Oncogene Proteins c-aktSESN2 protein, humanSestrinsAkt PKBApoptosisCancerCancer BiologyTumor

Identifiers

PMID25378405
PMCPMC4276849
OpenAlexW2012783067

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.