Abstract

BackgroundAcute lymphoblastic leukemia (ALL) is associated with higher levels of pro-inflammatory cytokines and oxidative stress. Recently, the levels of extracellular heat shock protein 72 (eHSP72) were found to be elevated in ALL, and its elevation associated with poor prognosis. Therefore, considering the possible role of eHSP72 as a modulator of the immunological system and metabolism, the aim of this study was to describe the response of eHSP72 to the induction phase of chemotherapy, along with metabolic, inflammatory and oxidative stress markers, in children and adolescents newly diagnosed with ALL.MethodsNineteen patients were recruited and analysed before and after the induction phase of chemotherapy (with 28 days of duration). Blood samples were taken for the analysis of C-reactive protein (CRP), levels of lipoperoxidation, insulin (and HOMA-IR), cortisol, glucose, lipid profile and eHSP72.ResultsWe found that induction phase of chemotherapy leads to a drop in glucose levels (from 101.79±19 to 75.8±9.7 mg/dL), improvements on inflammation (CRP levels, p<0.01) and oxidative stress (TBARS levels, p<0.01), reduction on eHSP72 (p=0.03) and improved insulin sensitivity (HOMA-IR, p=0.02).ConclusionOur results indicate that eHSP72 may have an immune and metabolic role and could be used as a marker of the treatment success and metabolic changes in children with ALL.

Highlights

  • Cancer development is often associated with chronic states of inflammation, hormonal unbalance, hyperinsulinemia and insulin resistance [1, 2]

  • We found that induction phase of chemotherapy leads to a drop in glucose levels, improvements on inflammation (CRP levels, p

  • Our results indicate that eHSP72 may have an immune and metabolic role and could be used as a marker of the treatment success and metabolic changes in children with Acute lymphoblastic leukemia (ALL)

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Summary

Introduction

Cancer development is often associated with chronic states of inflammation, hormonal unbalance, hyperinsulinemia and insulin resistance [1, 2]. There are growing evidences showing the role of low-grade inflammation in the pathogenesis of cancers, tumor growth and metastasis. Increased TNF-α signalling, for example, is responsible for several changes in target cells and tissues that may cause insulin resistance, skeletal muscle atrophy and oxidative stress [6]. Acute lymphoblastic leukemia (ALL) is associated with higher levels of pro-inflammatory cytokines and oxidative stress. Considering the possible role of eHSP72 as a modulator of the immunological system and metabolism, the aim of this study was to describe the response of eHSP72 to the induction phase of chemotherapy, along with metabolic, inflammatory and oxidative stress markers, in children and adolescents newly diagnosed with ALL

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