Author/Authors :
El-Benhawy، Sanaa A. نويسنده Radiation Science Department, Medical Research Institute, Alexandria University, Alexandria, Egypt , , Abd El-Moneim، Nadia Ahmed نويسنده Department of Cancer Management and Research, Medical Research Institute, Alexandria University, Alexandria, Egypt , , Ebeid، Samia A. نويسنده Applied Medical Chemistry Department, Medical Research Institute, Alexandria University, Alexandria, Egypt ,
Abstract :
Background: Recent epidemiological studies demonstrate that obesity is associated
with an increased risk for breast cancer in women. Increased estrogen levels are
suggested as one possible explanation, but this does not fully explain the relationship
between obesity and breast cancer. One alternative explanation is secretion by adipocytes
of metabolites, hormones and cytokines, collectively known as adipocytokines, which
regulate physiological and pathological processes. Among these adipokines are visfatin
and resistin. This study investigates whether visfatin or resistin in serum of breast cancer
patients can be used as potential diagnostic and prognostic tools for breast cancer, taking
into account clinicopathological features and anthropometric parameters.
Methods: Blood samples were collected from 70 breast cancer patients (35 obese
and 35 non-obese) and 20 healthy females matched for age and body mass index as
the control group. Serum visfatin levels were measured by enzyme linked immunosorbent
assay and serum resistin levels were measured by radioimmunoassay. Inflammatory
status was assessed by measuring C-reactive protein levels by an automated turbidimetric
analyzer.
Results: We observed highly elevated serum resistin and visfatin levels in breast
cancer patients compared to controls, independent of body mass index. Serum resistin
and visfatin levels were likely to be associated with increased breast cancer risk and
correlated with the inflammatory marker C-reactive protein.
Conclusion: Targeting resistin and visfatin inhibition can be an effective therapeutic
strategy in breast cancer by downregulating the inflammatory microenvironment in breast
tissue. Serum visfatin promises to be a novel biomarker of diagnostic and prognostic
value. Larger prospective studies are required to confirm our findings.