CD56 and CD11b Positivity with Low Smac/DIABLO Expression as Predictors of Chemoresistance in Acute Myeloid Leukaemia: Flow Cytometric Analysis

Asian Pac J Cancer Prev. 2018 Nov 29;19(11):3187-3192. doi: 10.31557/APJCP.2018.19.11.3187.

Abstract

Background: Resistance to chemotherapy is a major obstacle to curing acute myeloid leukaemia (AML), and several antigens are claimed to play primary roles in this resistance. Purpose: The aim of this study was to evaluate the roles of CD56, CD11b and Smac/DIABLO gene expression levels as prognostic markers of the clinical outcome, response to chemotherapy and survival of AML patients. Materials and Methods: A cross-sectional observational study was conducted on 60 naïve-AML patients who received induction therapy with mitoxantrone and cytarabine combined with a high dose of cytarabine. The CD56,CD11b and Smac/DIABLO expression levels were assessed using flow cytometry at diagnosis and were analysed for correlation with the possible associated risk factors, response to chemotherapy, and median duration of disease-free survival (DFS) and overall survival (OS). Results: The overall results revealed that AML patients who exhibited positive expression for CD56 and CD11b had short median durations of DFS and OS.(P = 0.019, 0.006, 0.029 and 0.024, respectively). Additionally, low Smac/DIABLO expression had a negative impact on treatment outcome in terms of CR rate (p=0.012) and reduced DFS (p=0.000) and OS(p=0.000) values. Conclusions: CD56 and CD11b positivity and low Smac/DIABLO expression are important predictive factors for the occurrence of chemoresistance, in addition to other risk factors, among AML patients.

Keywords: Chemoresistance; CD56; CD11b; Smac/DIABLO; AML.

Publication types

  • Observational Study

MeSH terms

  • Adolescent
  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Apoptosis Regulatory Proteins
  • Biomarkers, Tumor / metabolism*
  • CD11b Antigen / metabolism*
  • CD56 Antigen / metabolism*
  • Cross-Sectional Studies
  • Drug Resistance, Neoplasm*
  • Female
  • Flow Cytometry
  • Follow-Up Studies
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Leukemia, Myeloid, Acute / drug therapy
  • Leukemia, Myeloid, Acute / metabolism
  • Leukemia, Myeloid, Acute / pathology*
  • Male
  • Middle Aged
  • Mitochondrial Proteins / metabolism*
  • Prognosis
  • Survival Rate
  • Young Adult

Substances

  • Apoptosis Regulatory Proteins
  • Biomarkers, Tumor
  • CD11b Antigen
  • CD56 Antigen
  • DIABLO protein, human
  • ITGAM protein, human
  • Intracellular Signaling Peptides and Proteins
  • Mitochondrial Proteins
  • NCAM1 protein, human