The In Situ Expression of IL-6 and IL-1? in breast cancer patients

Authors

  • Amal H. Salman
  • Mayada N. Iqbal
  • Wasan A. Bakir

DOI:

https://doi.org/10.31351/vol17iss2pp55-62

Abstract

Breast cancer is the second most common cancer in women world. Multiple Cytokines appear to have a dominant role in human breast cancer formation. Estimation of the in situ expression of  IL-6 and IL-1β in breast cancer patients. A sixty patients with breast cancer BC were divided into two clinical subgroups, (30) with malignant breast cancer MBC and (30) with benign breast tumor as a control group according to histological examination. In situ hybridization technique used for detection of IL-6 and IL-1β mRNA sequence in two groups.  The results showed that percentages of mRNA expression of IL-6 and IL-1β were in (≥ 11-50%) for malignant breast cancer. This research also investigated that (73.3%) of benign breast tumor were expression less than (<10%) for   IL-6 and IL-1 β mRNA. The ISH expression  of the mean percentages of IL-6 and IL-1 β   were higher levels in malignant  breast cancer  patients ( 48.13 and 56.07 ,respectively) than benign  tumor (2.73 and 1.40 ,respectively), with highly significantly differences (P<0.01) of  ISH expression for  IL-6  and IL-1 β mRNA among two studied groups., the expression   of IL-6 and IL-1 β mRNA   are significantly elevated in the tissue of breast cancer patients compared with benign tumor and was found a significant correlation between the expression of IL- 6 and IL-1β mRNA in the tissue of breast cancer patients, thus the results of the present study might be explain the pathological role of these two cytokine in breast cancer.

Key words: IL-6 mRNA, IL-1β mRNA, Breast cancer, ISH.

 

How to Cite

1.
H. Salman A, N. Iqbal M, A. Bakir W. The In Situ Expression of IL-6 and IL-1? in breast cancer patients. Iraqi Journal of Pharmaceutical Sciences [Internet]. 2017 Mar. 30 [cited 2024 Dec. 19];17(2):55-62. Available from: https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/566

Publication Dates

Downloads

Published

2017-03-30