Effect of NUCKS-1 overexpression on cytokine profiling in obese women with breast cancer

Asian Pac J Cancer Prev. 2014;15(2):837-45. doi: 10.7314/apjcp.2014.15.2.837.

Abstract

Background: Overweight and obesity are recognized as major drivers of cancers including breast cancer. Several cytokines, including interleukin-6 (IL-6), IL-10 and lipocalin 2 (LCN2), as well as dysregulated cell cycle proteins are implicated in breast carcinogenesis. The nuclear, casein kinase and cyclin-dependent kinase substrate-1 (NUCKS-1), is a nuclear DNA-binding protein that has been implicated in several human cancers, including breast cancer.

Objectives: The present study was conducted to evaluate NUCKS-1 mRNA expression in breast tissue from obese patients with and without breast cancer and lean controls. NUCKS-1 expression was correlated to cytokine profiles as prognostic and monitoring tools for breast cancer, providing a molecular basis for a causal link between obesity and risk.

Materials and methods: This study included 39 females with breast cancer (G III) that was furtherly subdivided into two subgroups according to cancer grading (G IIIa and G IIIb) and 10 control obese females (G II) in addition to 10 age-matched healthy lean controls (G I). NUCKS-1 expression was studied in breast tissue biopsies by means of real-time PCR (RT-PCR). Serum cytokine profiles were determined by immunoassay. Lipid profiles and glycemic status as well as anthropometric measures were also recorded for all participants.

Results: IL-6, IL-12 and LCN2 were significantly higher in control obese and breast cancer group than their relevant lean controls (p<0.05), while NUCKS-1 mRNA expression was significantly higher in the breast cancer group compared to the other groups (p<0.05). Significant higher levels of IL-6, IL-12, and LCN2 as well as NUCKS-1 mRNA levels were reported in G IIIb than G IIIa, and positively correlated with obesity markers in all obese patients.

Conclusions: Evaluation of cytokine levels as well as related gene expression may provide a new tool for understanding interactions for three axes of carcinogenesis, innate immunity, inflammation and cell cycling, and hope for new strategies of management.

Publication types

  • Comparative Study

MeSH terms

  • Acute-Phase Proteins / genetics
  • Acute-Phase Proteins / metabolism*
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / complications
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Case-Control Studies
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Follow-Up Studies
  • Humans
  • Immunoenzyme Techniques
  • Interleukin-10 / genetics
  • Interleukin-10 / metabolism*
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Lipocalin-2
  • Lipocalins / genetics
  • Lipocalins / metabolism*
  • Middle Aged
  • Neoplasm Grading
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Obesity / complications
  • Obesity / genetics
  • Obesity / metabolism*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Prognosis
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*

Substances

  • Acute-Phase Proteins
  • Biomarkers, Tumor
  • Interleukin-6
  • LCN2 protein, human
  • Lipocalin-2
  • Lipocalins
  • NUCKS1 protein, human
  • Nuclear Proteins
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • Interleukin-10