IL-1β/IL-6 network in the tumor microenvironment of human colorectal cancer

Pathol Res Pract. 2018 Jul;214(7):986-992. doi: 10.1016/j.prp.2018.05.011. Epub 2018 May 20.

Abstract

Objectives: Recent studies suggest that the interaction between interleukin (IL)-1β and IL-6 in the microenvironment might be involved in the development and progression of human colorectal cancer (CRC). However, the expression of IL-1β/IL-6 network within the CRC microenvironment is not fully understood.

Materials and methods: The level of IL-1β/IL-6 network expression in 40 biopsies of sporadic CRC and 15 biopsies of controls was assessed using quantitative real-time polymerase chain reaction (PCR) assay, immunohistochemistry (IHC) and double immunofluorescence staining.

Results: Quantitative results obtained by real-time PCR revealed that both IL-1β and IL-6 mRNA expressions were increased in CRC tissues compared with expressions in controls. In which, IL-6 mRNA expression in primary CRC tissues showed a statistically significant relationship with tumor invasion depth. IHC observations confirmed that increased expression of IL-1β and IL-6 immunoreactivities was located in both the CRC epithelium and stroma. Furthermore, IHC results also revealed that increased expression of IL-1β receptor type 1 (IL-1R1) and IL-6 receptor (IL-6R) were observed in both CRC epithelial and stromal cells. IHCs in serial CRC sections and double immunofluorescence staining revealed a highly co-expression of IL-1R1 immunoreactivity with IL-6 immunoreactivity in the same cells, which confirmed a histological fundament of IL-1β/IL-6 network.

Conclusion: The IL-1β/IL-6 network is highly expressed in the CRC microenvironment, indicating that this network is important in the progression of CRC.

Keywords: Carcinogenesis; Colorectum; Interleukin-1β; Interlukin-6.

MeSH terms

  • Adenoma / pathology
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology
  • Disease Progression
  • Humans
  • Interleukin-1beta / metabolism*
  • Interleukin-6 / metabolism*
  • RNA, Messenger / genetics
  • Stromal Cells / pathology
  • Tumor Microenvironment / physiology*

Substances

  • IL6 protein, human
  • Interleukin-1beta
  • Interleukin-6
  • RNA, Messenger