HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Response to the methylation inhibitor dihydro-5-azacytidine in mesothelioma is not associated with methylation of p16INK4a: results of cancer and leukemia group B 159904.

AbstractINTRODUCTION:
The molecular mechanisms of oncogenesis in mesothelioma involve the loss of negative regulators of cell growth including p16INK4a. Absence of expression of the p16INK4a gene product is exhibited in virtually all mesothelioma tumors and cell lines examined to date. Loss of p16INK4a expression has also been frequently observed in more common neoplasms such as lung cancer as well. In a wide variety of these malignancies, including lung cancer, p16INK4a expression is known to be inactivated by hypermethylation of the first exon. This project (CALGB 159904) intended to test the hypothesis that in mesothelioma loss of p16INK4a via methylation would correlate with response to the cytidine analog and methylation inhibitor dihydro-5-azacytidine (DHAC).
METHODS:
Using tissue samples from CALGB 8833 and 9031, two clinical studies which used DHAC based therapy in mesothelioma, this study tested the hypothesis that tumors possessing methylation of p16INK4a would have a better response and survival following DHAC treatment than their nonmethylated counterparts.
RESULTS:
Methylation of p16INK4a was identified in 4 of the 20 specimens. Although there was a trend towards improved survival the result was not statistically significant.
CONCLUSIONS:
There was no significant correlation between the presence of p16INK4a methylation and response to DHAC therapy or overall survival.
AuthorsRobert A Kratzke, Xiaofei Wang, Long Wong, Marian G Kratzke, Mark R Green, Everett E Vokes, Nicholas J Vogelzang, Hedy L Kindler, Jeffrey A Kern, Cancer and Leukemia Group B
JournalJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer (J Thorac Oncol) Vol. 3 Issue 4 Pg. 417-21 (Apr 2008) ISSN: 1556-1380 [Electronic] United States
PMID18379362 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Antimetabolites, Antineoplastic
  • Cyclin-Dependent Kinase Inhibitor p16
  • 5,6-dihydro-5-azacytidine
  • Azacitidine
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Antimetabolites, Antineoplastic (pharmacology)
  • Azacitidine (analogs & derivatives, pharmacology)
  • Cyclin-Dependent Kinase Inhibitor p16 (genetics)
  • DNA Methylation (drug effects)
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Mesothelioma (drug therapy, genetics, pathology)
  • Middle Aged
  • Polymerase Chain Reaction
  • Prognosis
  • Survival Rate

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: