Author/Authors :
Jaberipour، Mansooreh نويسنده Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran , , Baharlou، Rasoul نويسنده Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran , , Zavaran Hosseini، Ahmad نويسنده , , Talei، Abdolrasoul نويسنده , , Razmkhah، Mahboobeh نويسنده Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran , , Ghaderi، Abbas نويسنده ,
Abstract :
Background: Several recent studies demonstrated that transforming growth factor
beta (TGF-B), by stimulating T regulatory cells, and interleukins 6 and 17 (IL-6, IL-
17), by inducing inflammatory reactions, may be critical factors in cancer pathogenesis.
Methods: We used quantitative real-time polymerase chain reaction assays to
quantify the expression of IL-17, IL-6 and TGF-B mRNA in peripheral blood
mononuclear cells and lymphocytes from draining lymph nodes of 60 women with breast
cancer. The results were compared according to the patients’ clinical or pathological
status.
Results: Higher amounts of IL-17 and IL-6 mRNA, but not TGF-B transcripts, were
found in patients compared to controls. There were no significant differences between
patients with negative or positive nodes or with different histological grades or stages
of disease.
Conclusion: Most women in this analysis had stage I or II disease. We thus
conclude that IL-17, a prominent proinflammatory cytokine, may play an important
role in recruiting and infiltrating antitumor immune responses in early stages of breast
cancer.