Abstract

Breast cancer is associated with obesity, possibly due to direct effects of adipokines and myokines, such as omentin-1 and irisin. In this study, we aimed to evaluate omentin-1 and irisin levels in women with benign and/or malignant breast neoplasms vs. healthy controls. Disease-free individuals (N = 56) and patients with histologically proven benign (N = 61) or malignant tumor (N = 96; subdivided into recently diagnosed/treatment-naïve (N = 72) and chemotherapy-treated (N = 24) subgroups) were enrolled in this study. Demographic, biochemical, and tumor histological characteristics were recorded. Body composition parameters were assessed using bioelectrical impedance. Serum irisin and omentin-1 levels were quantified with ELISA kits. In adjusted models, irisin levels were higher in both benign and malignant cases compared to controls but were comparable between neoplasms. Further adjustment for omentin-1 levels showed that age (odds ratio (OR) = 1.05, 95% confidence interval (95% CI) = (1.02, 1.08), p < 0.01) and irisin levels (OR = 5.30, 95% CI = (1.24, 22.38), p=0.03) were independent predictors of the presence of malignancy. These molecules were associated with each other and with other anthropometric and demographic parameters. Irisin was associated with tumor histological characteristics including Ki67% levels, Elston-Ellis grading system, and estrogen receptors status. Omentin-1 was also associated with the Elston-Ellis grading system. In conclusion, serum irisin is increased in patients with both benign and malignant diseases of the breast. When combined with omentin-1, irisin concentration was associated with the presence of breast malignancy. This molecule's role as a potential diagnostic and/or prognostic agent in breast malignancies warrants further investigation in larger prospective studies.

Highlights

  • Academic Editor: Genaro Barrientos ese molecules were associated with each other and with other anthropometric and demographic parameters

  • In raw comparisons, treatment-naıve cancer group patients had significantly higher logarithmically (Ln) transformed omentin-1 levels compared to healthy controls (p 0.02) (Figure 1(a))

  • Post hoc comparison between healthy control and chemotherapy-treated group subjects was borderline significant (p 0.06), but significance was lost after adjustment for age (p 0.13), and this result remained unaffected after further adjustment for Body Mass Index (BMI), serum glucose, and total cholesterol (p for trend >0.05 for all) (Figure 1(a))

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Summary

Introduction

Academic Editor: Genaro Barrientos ese molecules were associated with each other and with other anthropometric and demographic parameters. The prototype adipokine, was increased in patients with breast malignancies and was positively associated with disease progression in vitro [4], serum adiponectin, a beneficial adipokine, was lower in breast cancer patients [5] and induced apoptosis and cell death in breast cancer cell lines [6]. Irisin levels were lower in breast cancer patients compared to healthy controls, but in the same study, a positive association with tumor histology was shown [17]. It is currently unknown whether these molecules could be used as noninvasive diagnostic markers for the timely diagnosis of breast benign or to discriminate between benign growths and malignancies

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