Evidence map›Paper›PMID 22123174›Full record

ArticleCancer biology & therapy2011

Norcantharidin induces melanoma cell apoptosis through activation of TR3 dependent pathway.

Shujing Liu, Hong Yu, Suresh M Kumar, James S Martin, Zhanyong Bing, Weiqi Sheng, Marcus Bosenberg, Xiaowei Xu

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  5. Review
  6. Loss of Phd2 cooperates with BRAFNature communications · 2018
    Article
  7. A Designer Cross-reactive DNA Immunotherapeutic Vaccine that Targets Multiple MAGE-A Family Members Simultaneously for Cancer Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. TR3 is preferentially expressed by bulge epithelial stem cells in human hair follicles.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  13. Article
  14. 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 4 institutions in 2 countries.

Shujing LiuDepartment of Pathology, University of Pennsylvania School of Medicine, Philadelphia, USA.
Hong Yu
Suresh M Kumar
James S Martin
Zhanyong Bing
Weiqi Sheng
Marcus Bosenberg
Xiaowei Xu
Philadelphia University · USUniversity of Pennsylvania · USShanghai Cancer Institute · CNUniversity of New Haven · US

Funding

Tissue &PathologyP50CA093372 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2001 to 2009
$15.4M
Characterization of neural crest stem cells in human hair follicles.R01AR054593 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI XU, XIAOWEI · 2009 to 2013
$1.9M
Ultrasensitive FACTT assays for serum biomarkersR21CA116103 · NCI · UNIVERSITY OF PENNSYLVANIA · PI XU, XIAOWEI · 2007 to 2008
$389k
NCI NIH HHS CA-093372NCI NIH HHS CA-116103NCI NIH HHS P50 CA093372NCI NIH HHS R21 CA116103NIAMS NIH HHS AR-054593NIAMS NIH HHS R01 AR054593
6 · The paper itself

Abstract

Norcantharidin (NCTD) has been reported to induce tumor cell apoptosis. However, the underlying mechanism behinds its antitumor effect remains elusive. We have previously shown that TR3 expression is significantly decreased in metastatic melanomas and involved in melanoma cell apoptosis. In this study, we showed that NCTD inhibited melanoma cell proliferation and induced apoptosis in a dose related manner. NCTD induced translocation of TR3 from nucleus to mitochondria where it co-localized with Bcl-2 in melanoma cells. NCTD also increased cytochome c release from mitochondria to the cytoplasm. These changes were accompanied by increased expression of Bax and cleaved caspase-3 along with decreased expression of Bcl2 and NF-κB2. The effects of NCTD were inhibited by knockdown of TR3 expression using TR3 specific shRNA in melanoma cells. Furthermore, NCTD significantly decreased tumor volume and improved survival of Tyr::CreER; BRAF(Ca/+); Pten(lox/lox) transgenic mice. Our data indicates that NCTD inhibits melanoma growth by inducing tumor cell apoptosis via activation of a TR3 dependent pathway. These results suggest that NCTD is a potential therapeutic agent for melanoma.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBridged Bicyclo Compounds, HeterocyclicCell Line, TumorCell ProliferationHumansMelanomaMiceMice, TransgenicMitochondriaNuclear Receptor Subfamily 4, Group A, Member 1Protein BindingProtein TransportProto-Oncogene Proteins c-bcl-2Signal TransductionAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicnorcantharidinNuclear Receptor Subfamily 4, Group A, Member 1Proto-Oncogene Proteins c-bcl-2

Identifiers

PMID22123174
PMCPMC3280911
OpenAlexW2005450888

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.