Dysregulation of over-expressed IL-32 in colorectal cancer induces metastasis

Yi Yang1, Zihao Wang2, Yiming Zhou3

  • 1Department of General Surgery, Huashan Hospital Affiliated to Fudan University, Floor 16, Building 2, 12 Wulumuqizhong Road, Shanghai, 200040, China. fengwu822@qq.com.

Abstract

Insights

Interleukin-32 (IL-32) expression is significantly higher in colorectal cancer (CRC) metastases than in primary tumors. This suggests IL-32 may drive CRC metastasis, including lymph node involvement.

Area of Science:

  • Oncology
  • Immunology
  • Molecular Biology

Background:

  • Interleukin-32 (IL-32) is an intracellular mediator of inflammation.
  • IL-32 signaling involves NF-κB and STAT3 pathways.

Purpose of the Study:

  • To investigate the clinical significance of IL-32 expression in colorectal cancer (CRC) metastasis.
  • To determine if IL-32 correlates with CRC organic and lymph node metastasis.

Main Methods:

  • Immunohistochemistry was used to detect IL-32 expression in 70 CRC patient samples.
  • Samples included primary CRC lesions and metastatic lesions.
  • Statistical analysis correlated IL-32 expression with metastasis status.

Main Results:

  • IL-32 positive rates were significantly higher in CRC organic metastasis compared to primary CRC (P < 0.05).
  • IL-32 positive rates were significantly higher in primary CRC with lymph node metastasis than without (P < 0.05).

Conclusions:

  • IL-32 expression levels may influence the N stage (lymph node metastasis) of CRC.
  • IL-32 may play a role in promoting organic and lymph node metastasis in colorectal cancer.