Evidence map›Paper›PMID 22496897›Full record

ArticlePloS one2012

Rational incorporation of selenium into temozolomide elicits superior antitumor activity associated with both apoptotic and autophagic cell death.

Yan Cheng, Ugir Hossain Sk, Yi Zhang, Xingcong Ren, Li Zhang, Kathryn J Huber-Keener, Yuan-Wan Sun, Jason Liao, Shantu Amin, Arun K Sharma and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Selenium enhances TRPA1 channel-mediated activity of temozolomide in SH-SY5Y neuroblastoma cells.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Friend or foe? The current epidemiologic evidence on selenium and human cancer risk.Journal of environmental science and health. Part C, Environmental carcinogenesis & ecotoxicology reviews · 2013
    Review
  18. 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

11 authors at 1 institution in 1 country.

Yan ChengDepartment of Pharmacology and The Penn State Hershey Cancer Institute, The Pennsylvania State University College of Medicine and Milton S Hershey Medical Center, Hershey, Pennsylvania, United States of America.
Ugir Hossain Sk
Yi Zhang
Xingcong Ren
Li Zhang
Kathryn J Huber-Keener
Yuan-Wan Sun
Jason Liao
Shantu Amin
Arun K Sharma
Jin-Ming Yang
Penn State Milton S. Hershey Medical Center · US

Funding

Autophagy in Brain TumorR01CA135038 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI YANG, JIN-MING · 2009 to 2013
$1.6M
ISC-4 as a Novel Lung Cancer Chemopreventive AgentR03CA143999 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SHARMA, ARUN K · 2009 to 2010
$153k
NCI NIH HHS R01 CA135038NCI NIH HHS R01CA135038NCI NIH HHS R03 CA143999NCI NIH HHS R03CA143999
6 · The paper itself

Abstract

backgroundThe DNA alkylating agent temozolomide (TMZ) is widely used in the treatment of human malignancies such as glioma and melanoma. On the basis of previous structure-activity studies, we recently synthesized a new TMZ selenium analog by rationally introducing an N-ethylselenocyanate extension to the amide functionality in TMZ structure. PRINCIPAL

findingsThis TMZ-Se analog showed a superior cytotoxicity to TMZ in human glioma and melanoma cells and a more potent tumor-inhibiting activity than TMZ in mouse glioma and melanoma xenograft model. TMZ-Se was also effective against a TMZ-resistant glioma cell line. To explore the mechanism underlying the superior antitumor activity of TMZ-Se, we compared the effects of TMZ and TMZ-Se on apoptosis and autophagy. Apoptosis was significantly increased in tumor cells treated with TMZ-Se in comparison to those treated with TMZ. TMZ-Se also triggered greater autophagic response, as compared with TMZ, and suppressing autophagy partly rescued cell death induced by TMZ-Se, indicating that TMZ-Se-triggered autophagy contributed to cell death. Although mRNA level of the key autophagy gene, Beclin 1, was increased, Beclin 1 protein was down-regulated in the cells treated with TMZ-Se. The decrease in Beclin 1 following TMZ-Se treatment were rescued by the calpain inhibitors and the calpain-mediated degradation of Beclin1 had no effect on autophagy but promoted apoptosis in cells treated with TMZ-Se.

conclusionsOur study indicates that incorporation of Se into TMZ can render greater potency to this chemotherapeutic drug.

Indexed as

AnimalsAntineoplastic Agents, AlkylatingApoptosisApoptosis Regulatory ProteinsAutophagyBeclin-1Brain NeoplasmsCalpainCell Line, TumorDacarbazineGliomaHumansMaleMelanomaMembrane ProteinsMiceAntineoplastic Agents, AlkylatingApoptosis Regulatory ProteinsBeclin-1BECN1 protein, humanBecn1 protein, mouseCalpainDacarbazineMembrane ProteinsSeleniumTemozolomide

Identifiers

PMID22496897
PMCPMC3320619
OpenAlexW2072953109

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.