The Chemokine CXCL8 in Carcinogenesis and Drug Response

Author:

Gales Dominique1ORCID,Clark Clarence2,Manne Upender3,Samuel Temesgen1ORCID

Affiliation:

1. Center for Cancer Research and Department of Pathobiology, Tuskegee University, 1200 Old Montgomery Road, School of Veterinary Medicine, Tuskegee, AL 36830, USA

2. Morehouse School of Medicine, 720 Westview Drive, S.W., Atlanta, GA 30310, USA

3. Department of Pathology, and Comprehensive Cancer Center, University of Alabama, Birmingham, 1720 Second Avenue South, AL 35294, USA

Abstract

Although the functions of chemokines in the regulation of immune processes have been studied in some detail, the role of these biomolecules in cancer is not fully understood. Chemokines mediate migration of immune cells and other functions related to immunity. They are also involved in oncogenesis and in tumor progression, invasion, and metastasis through mechanisms similar to their roles in immune functions. Various chemokines also promote cell proliferation and resistance to apoptosis of stressed cells. Consequently, chemokines and their receptors present potential therapeutic targets for anticancer drugs. The chemokine CXCL8, also known as interleukin-8 (IL8), is a proinflammatory molecule that has functions within the tumor microenvironment. Due to its potent angiogenic effects and the activity of the chemokine and its receptors in the promotion of invasion and metastasis, CXCL8 and its receptors are now considered as attractive targets for cancer therapy. This review relates the current understanding of the regulation, signaling, and functions of CXCL8 that contribute to tumor growth and metastasis, and of its role in drug response.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

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