Evidence map›Paper›PMID 17030815›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Intrinsic apoptotic and thioredoxin pathways in human prostate cancer cell response to histone deacetylase inhibitor.

Weisheng Xu, Lang Ngo, Gisela Perez, Milos Dokmanovic, Paul A Marks

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
–field-weighted citation impact
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

79 citing papers in PubMed.

  1. Vorinostat (NSC# 701852) in patients with relapsed non-small cell lung cancer: a Wisconsin Oncology Network phase II study.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2009
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The application of histone deacetylases inhibitors in glioblastoma.Journal of experimental & clinical cancer research : CR · 2020
    Review
  8. Article
  9. The Roles of Histone Deacetylases and Their Inhibitors in Cancer Therapy.Frontiers in cell and developmental biology · 2020
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Upregulation of connexin43 contributes to PX-12-induced oxidative cell death.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  20. Review

19 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

5 authors.

Weisheng XuMemorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Lang Ngo
Gisela Perez
Milos Dokmanovic
Paul A Marks

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS CA-008748NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

There is a great need to develop better mechanism-based therapies for prostate cancer. In this investigation, we studied four human prostate cancer cell lines, LNCaP, DU145, LAPC4, and PC3, which differ in response to the histone deacetylase inhibitor, suberoylanilide hydroxamic acid (vorinostat), a new anticancer drug. Examining the role of intrinsic mitochondrial caspase-dependent apoptosis and caspase-independent, reactive oxygen species (ROS) facilitated cell death, has provided an understanding of mechanisms that may determine the varied response to the histone deacetylase inhibitor. We found striking differences among these cancer cells in constitutive expression and response to suberoylanilide hydroxamic acid in levels of antiapoptotic and proapoptotic proteins, mitochondria membrane integrity, activation of caspases, ROS accumulation, and expression of thioredoxin, the major scavenger of ROS. Identifying these differences can have predictive value in assessing therapeutic response and identifying targets to enhance therapeutic efficacy.

Indexed as

Histone Deacetylase InhibitorsAntineoplastic AgentsApoptosisApoptosis Regulatory ProteinsCarrier ProteinsCaspase InhibitorsCaspasesCell Line, TumorHumansHydroxamic AcidsInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsMaleMicrotubule-Associated ProteinsMitochondriaMitochondrial ProteinsAntineoplastic AgentsApoptosis Regulatory ProteinsBIRC5 protein, humanCarrier ProteinsCaspase InhibitorsCaspasesDIABLO protein, humanHistone Deacetylase InhibitorsHydroxamic AcidsInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsMicrotubule-Associated ProteinsMitochondrial ProteinsNeoplasm ProteinsReactive Oxygen SpeciesSurvivinThioredoxinsTXNIP protein, humanVorinostatXIAP protein, humanX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID17030815
PMCPMC1592530

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.