Molecular cross-talk of IL-6 in tumors and new progress in combined therapy

Thorac Cancer. 2018 Jun;9(6):669-675. doi: 10.1111/1759-7714.12633. Epub 2018 Mar 30.

Abstract

IL-6, a cytokine activated by type I interferons (IFNs), is encoded by the IL-6 gene, and secreted by T cells and macrophages. It serves many purposes in the human body and is significant to pathological and physiological activities, such as acute inflammatory responses, autoimmune diseases, and tumor formation. The wide range of IL-6 actions on tumors rely on more than one specific pathway. Advances in modern research have determined that to fulfill its complex physiological functions, IL-6 must be involved in cross-talk with a number of other molecular pathways. Therefore, it is important to clarify the comprehensive pathway network associated with IL-6 activity and to explore the mechanisms to inhibit its pathological activity in order to develop corresponding treatment plans. This study is a simple review of the pathological and physiological actions of IL-6 on the human body. It explains in detail the molecular pathways involved in cross-talk between IL-6 and tumors, summarizing and discussing the latest progress made in IL-6-related internal medicine treatments in recent years, including chemotherapies, targeted therapies, and immunotherapies. Our results provide new insight into the treatment of tumors.

Keywords: Combined therapy; IL-6; cross-talk; new progress; tumor.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cisplatin / pharmacology
  • Drug Resistance, Neoplasm* / drug effects
  • Drug Resistance, Neoplasm* / physiology
  • ErbB Receptors / metabolism
  • Humans
  • Immunotherapy / methods
  • Interleukin-6 / antagonists & inhibitors*
  • Interleukin-6 / immunology
  • Interleukin-6 / physiology*
  • Molecular Targeted Therapy / methods
  • NF-kappa B / metabolism
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • STAT2 Transcription Factor / metabolism
  • STAT3 Transcription Factor / metabolism

Substances

  • IL6 protein, human
  • Interleukin-6
  • NF-kappa B
  • STAT2 Transcription Factor
  • STAT2 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • EGFR protein, human
  • ErbB Receptors
  • Cisplatin