Chemokine Like Receptor-1 (CMKLR-1) Receptor: A Potential Therapeutic Target in Management of Chemerin Induced Type 2 Diabetes Mellitus and Cancer

Curr Pharm Des. 2017;23(25):3689-3698. doi: 10.2174/1381612823666170616081256.

Abstract

Background: Chemerin is an adipokine that induces insulin resistance by the mechanism of inflammation in adipose tissue but these are still unclear. A high level of chemerin in humans is considered as a marker of inflammation in insulin resistance and obesity as well as in type 2 diabetes mellitus. Despite the role of chemerin in insulin resistance progression, chemerin as one of the novel adipokines is proposed to be involved in high cancer risk and mortality.

Aim: The aim of this paper was to review the role of CMKLR-1 receptor and the potential therapeutic target in the management of chemerin induced type 2 diabetes mellitus and cancer.

Pathophysiology: Increased chemerin secretion activates an inflammatory response. The inflammatory response will increase the oxidative stress in adipose tissue and consequently results in an insulin-resistant state. The occurrence of inflammation, oxidative stress and insulin resistance leads to the progression of cancers.

Conclusion: Chemerin is one of the markers that may involve in development of both cancer and insulin resistance. Chemokine like receptor- 1 (CMKLR-1) receptor that regulates chemerin levels exhibits a potential therapeutic target for insulin resistance, type 2 diabetes and cancer treatment.

Keywords: Chemerin; cancer; chemokine-like receptor 1; inflammation; insulin resistance; obesity; therapeutic target; type 2 diabetes mellitus.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / metabolism
  • Case-Control Studies
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / metabolism*
  • Disease Management
  • Drug Delivery Systems / methods
  • Drug Delivery Systems / trends*
  • Humans
  • Hypoglycemic Agents / administration & dosage*
  • Hypoglycemic Agents / metabolism
  • Insulin Resistance / physiology
  • Neoplasms / drug therapy
  • Neoplasms / metabolism*
  • Receptors, Chemokine / antagonists & inhibitors
  • Receptors, Chemokine / metabolism*

Substances

  • Antineoplastic Agents
  • CMKLR1 protein, human
  • Hypoglycemic Agents
  • Receptors, Chemokine