HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Survivin expression predicts poorer prognosis in anaplastic large-cell lymphoma.

AbstractPURPOSE:
Survivin, a member of the inhibitor of apoptosis (IAP) family, is not detected in normal adult tissues but is overexpressed in various cancers, including some types of lymphoma. The frequency and prognostic significance of survivin expression in anaplastic large-cell lymphoma (ALCL) is unknown.
MATERIALS AND METHODS:
We assessed for survivin expression in 62 ALCL tumors (30 anaplastic lymphoma kinase [ALK]-positive and 32 ALK-negative) obtained before doxorubicin-based chemotherapy. Given that survivin is a target of the STAT3 signaling pathway and STAT3 is activated in ALCL, survivin expression was also correlated with STAT3 activation.
RESULTS:
Survivin was expressed in 34 tumors (55%) and did not correlate with ALK. A significant association between survivin expression and STAT3 activation was observed (P =.007, Fisher's exact test). For the ALK-positive group, the 5-year failure-free survival (FFS) was 34% for patients with survivin-positive ALCL compared with 100% for patients with survivin-negative ALCL (P =.009, log-rank test). For the ALK-negative group, the 5-year FFS was 46% for patients with survivin-positive tumors compared with 89% for patients with survivin-negative tumors (P =.03, log-rank test). Overall survival was similarly worse for patients with survivin-positive tumors in both the ALK-positive and ALK-negative groups. Furthermore, multivariate analysis confirmed the independent prognostic value of survivin expression, along with age older than 60 years and Ann Arbor stage III or IV.
CONCLUSION:
Survivin is expressed in approximately half of ALCL tumors and independently predicts unfavorable clinical outcome. Modulation of survivin expression or function may provide a novel target for experimental therapy in patients with ALCL.
AuthorsEllen J Schlette, L Jeffrey Medeiros, Andre Goy, Raymond Lai, George Z Rassidakis
JournalJournal of clinical oncology : official journal of the American Society of Clinical Oncology (J Clin Oncol) Vol. 22 Issue 9 Pg. 1682-8 (May 01 2004) ISSN: 0732-183X [Print] United States
PMID15117990 (Publication Type: Journal Article)
Chemical References
  • Acute-Phase Proteins
  • BIRC5 protein, human
  • DNA-Binding Proteins
  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Survivin
  • Trans-Activators
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases
Topics
  • Acute-Phase Proteins
  • Adult
  • Age Factors
  • Anaplastic Lymphoma Kinase
  • Apoptosis
  • DNA-Binding Proteins (analysis, biosynthesis)
  • Female
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Lymphoma, Large B-Cell, Diffuse (genetics, pathology)
  • Male
  • Microtubule-Associated Proteins (biosynthesis)
  • Multivariate Analysis
  • Neoplasm Proteins
  • Neoplasm Staging
  • Predictive Value of Tests
  • Prognosis
  • Protein-Tyrosine Kinases (analysis, biosynthesis)
  • Receptor Protein-Tyrosine Kinases
  • STAT3 Transcription Factor
  • Signal Transduction
  • Survival Analysis
  • Survivin
  • Trans-Activators (analysis, biosynthesis)

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: