Comparative analysis of survivin expression in untreated and relapsed canine lymphoma

J Vet Intern Med. 2008 Jul-Aug;22(4):989-95. doi: 10.1111/j.1939-1676.2008.0143.x.

Abstract

Background: Survivin, a member of the inhibitor of apoptosis protein family, has a dual role in tumor cell proliferative and antiapoptotic pathways. Survivin expression has been shown to be a negative prognostic factor in several cancers of humans, including B-cell non-Hodgkin's lymphoma.

Hypotheses: High survivin expression will be a negative prognostic factor in dogs with lymphoma (LSA) treated with chemotherapy. In addition, survivin expression will be upregulated in relapsed canine LSA when compared with patient-matched, pretreatment biopsies.

Animals: Thirty-one client-owned dogs with stage IIIa or IVa LSA.

Methods: Retrospective evaluation of survivin immunoreactivity was performed on pretreatment lymph node biopsies and patient-matched samples obtained from dogs at relapse after being treated with an abbreviated CHOP-based protocol.

Results: In this population of dogs presenting with stage IIIa or IVa B-cell LSA, those dogs that had high survivin immunoreactivity scores had a significantly (P < .01, hazard ratio = 0.30) shorter median disease-free interval than did dogs with low survivin immunoreactivity scores (171 days versus 321 days, respectively). Survivin immunoreactivity was not significantly different in relapsed canine LSA when compared with patient-matched, pretreatment biopsies.

Conclusions and clinical importance: Survivin expression is a negative prognostic factor that can predict early treatment failure of dogs that present with stage IIIa or IVa, B-cell LSA when treated with a CHOP-based protocol.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cyclophosphamide / therapeutic use
  • Dog Diseases / drug therapy
  • Dog Diseases / metabolism*
  • Dogs
  • Doxorubicin / therapeutic use
  • Female
  • Gene Expression Regulation, Neoplastic
  • Lymphoma / drug therapy
  • Lymphoma / metabolism
  • Lymphoma / veterinary*
  • Male
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Prednisone / therapeutic use
  • Recurrence
  • Time Factors
  • Vincristine / therapeutic use

Substances

  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Vincristine
  • Doxorubicin
  • Cyclophosphamide
  • Prednisone

Supplementary concepts

  • CHOP protocol