The intricate role of CXCR4 in cancer

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Chemokines mediate numerous physiological and pathological processes related primarily to cell homing and migration. The chemokine CXCL12, also known as stromal cell-derived factor-1, binds the G-protein-coupled receptor CXCR4, which, through multiple divergent pathways, leads to chemotaxis, enhanced intracellular calcium, cell adhesion, survival, proliferation, and gene transcription. CXCR4, initially discovered for its involvement in HIV entry and leukocytes trafficking, is overexpressed in more than 23 human cancers. Cancer cell CXCR4 overexpression contributes to tumor growth, invasion, angiogenesis, metastasis, relapse, and therapeutic resistance. CXCR4 antagonism has been shown to disrupt tumor-stromal interactions, sensitize cancer cells to cytotoxic drugs, and reduce tumor growth and metastatic burden. As such, CXCR4 is a target not only for therapeutic intervention but also for noninvasive monitoring of disease progression and therapeutic guidance. This review provides a comprehensive overview of the biological involvement of CXCR4 in human cancers, the current status of CXCR4-based therapeutic approaches, as well as recent advances in noninvasive imaging of CXCR4 expression.

Original languageEnglish (US)
Title of host publicationAdvances in Cancer Research
PublisherAcademic Press Inc.
Pages31-82
Number of pages52
DOIs
StatePublished - Jan 1 2014

Publication series

NameAdvances in Cancer Research
Volume124
ISSN (Print)0065-230X
ISSN (Electronic)2162-5557

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Keywords

  • Cancer therapy
  • Chemokine receptor
  • Chemotaxis
  • CXCL12
  • CXCR4 inhibitor
  • CXCR4 tracers
  • Metastasis
  • Molecular imaging
  • PET-CT
  • Therapeutic intervention

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Chatterjee, S., Behnam Azad, B., & Nimmagadda, S. (2014). The intricate role of CXCR4 in cancer. In Advances in Cancer Research (pp. 31-82). (Advances in Cancer Research; Vol. 124). Academic Press Inc.. https://doi.org/10.1016/B978-0-12-411638-2.00002-1