HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

FANCD2 expression in advanced non-small-cell lung cancer and response to platinum-based chemotherapy.

Abstract
Fanconi's anemia (FA) is a genetically heterogeneous disease characterized by cancer susceptibility and hypersensitivity to cross-linking agents such as cisplatin. Recently, inactivation of the FA pathway has been proposed to contribute to genomic instability and an increased sensitivity to cisplatin-based therapy in a subset of ovarian tumors. Platinum-based chemotherapy constitutes standard systemic therapy for advanced non-small-cell lung cancer (NSCLC), but resistance to platinum chemotherapy is common. In this study, we evaluated the status of the FA pathway in tumor samples derived from patients with NSCLC in relation to their response to platinum-based chemotherapy. For this purpose, we assessed the expression of FANCD2 protein (a marker for FA pathway functioning) by immunohistochemistry in tumor specimens from 47 patients treated with platinum-based chemotherapy. FANCD2 expression could be detected in 32% of the cases (15 of 47). Expression of FANCD2 was not correlated with any patient or tumor characteristics, and FANCD2 expression was not a predictor of response to chemotherapy or patient survival. In conclusion, the activation status of the FA pathway had no value in predicting sensitivity to platinum-based chemotherapy in patients with advanced NSCLC.
AuthorsMiriam Ferrer, Simone W Span, Barbara Vischioni, Joost J Oudejans, Paul J van Diest, Johan P de Winter, Giuseppe Giaccone, Frank A E Kruyt
JournalClinical lung cancer (Clin Lung Cancer) Vol. 6 Issue 4 Pg. 250-4 (Jan 2005) ISSN: 1525-7304 [Print] United States
PMID15694018 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • FANCD2 protein, human
  • Fanconi Anemia Complementation Group D2 Protein
  • Nuclear Proteins
  • Cisplatin
Topics
  • Adult
  • Aged
  • Antineoplastic Agents (therapeutic use)
  • Carcinoma, Non-Small-Cell Lung (drug therapy, metabolism, pathology)
  • Cisplatin (therapeutic use)
  • Fanconi Anemia Complementation Group D2 Protein
  • Female
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms (drug therapy, metabolism, pathology)
  • Male
  • Middle Aged
  • Nuclear Proteins (metabolism)

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: