Novel therapies for metastatic castrate-resistant prostate cancer

J Natl Cancer Inst. 2011 Nov 16;103(22):1665-75. doi: 10.1093/jnci/djr362. Epub 2011 Sep 13.

Abstract

Recent advances in tumor biology have made remarkable achievements in the development of therapy for metastatic castrate-resistant prostate cancer. These advances reflect a growing appreciation for the role of the tumor microenvironment in promoting prostate cancer progression. Prostate cancer is no longer viewed predominantly as a disease of abnormally proliferating epithelial cells but rather as a disease of complex interactions between prostate cancer epithelial cells (epithelial compartment) and the surrounding tissues (stromal compartment) in which they reside. For example, prostate cancers frequently metastasize to bone, an organ that contains a microenvironment rich in extracellular matrix proteins and stromal cells including hematopoietic cells, osteoblasts, osteoclasts fibroblasts, endothelial cells, adipocytes, immune cells, and mesenchymal stem cells. Multiple signaling pathways provide crosstalk between the epithelial and the stromal compartments to enhance tumor growth, including androgen receptor signaling, tyrosine kinase receptor signaling, and immune surveillance. The rationale to disrupt this "two-compartment" crosstalk has led to the development of drugs that target tumor stromal elements in addition to the cancer epithelial cell.

Trial registration: ClinicalTrials.gov NCT00861614 NCT01057810.

Publication types

  • Review

MeSH terms

  • Androstenes
  • Androstenols / pharmacology
  • Angiogenesis Inhibitors / pharmacology
  • Anilides / pharmacology
  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal, Humanized / pharmacology
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Antineoplastic Agents, Hormonal / pharmacology
  • Atrasentan
  • Benzamides
  • Bevacizumab
  • Biomarkers, Tumor / blood
  • Bone Remodeling / drug effects
  • Cancer Vaccines / immunology
  • Cancer Vaccines / pharmacology*
  • Clinical Trials as Topic
  • Clusterin / pharmacology
  • Dasatinib
  • Denosumab
  • Endothelin-1 / antagonists & inhibitors
  • Humans
  • Immunotherapy / methods
  • Indoles / pharmacology
  • Ipilimumab
  • Male
  • Mice
  • Mice, SCID
  • Molecular Targeted Therapy* / methods
  • Nitriles
  • Orchiectomy
  • Phenylthiohydantoin / analogs & derivatives
  • Phenylthiohydantoin / pharmacology
  • Prostate-Specific Antigen / blood
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / immunology
  • Prostatic Neoplasms / pathology*
  • Pyridines / pharmacology
  • Pyrimidines / pharmacology
  • Pyrroles / pharmacology
  • Pyrrolidines / pharmacology
  • RANK Ligand / antagonists & inhibitors
  • RANK Ligand / pharmacology
  • Receptor Cross-Talk / drug effects*
  • Receptors, Androgen / drug effects
  • Signal Transduction / drug effects*
  • Sunitinib
  • Taxoids / pharmacology
  • Thiazoles / pharmacology
  • Tissue Extracts / pharmacology
  • Treatment Failure
  • Tumor Microenvironment / drug effects*
  • Xenograft Model Antitumor Assays

Substances

  • Androstenes
  • Androstenols
  • Angiogenesis Inhibitors
  • Anilides
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Antineoplastic Agents, Hormonal
  • Benzamides
  • Biomarkers, Tumor
  • Cancer Vaccines
  • Clusterin
  • Endothelin-1
  • Indoles
  • Ipilimumab
  • Nitriles
  • Pyridines
  • Pyrimidines
  • Pyrroles
  • Pyrrolidines
  • RANK Ligand
  • Receptors, Androgen
  • TNFSF11 protein, human
  • Taxoids
  • Thiazoles
  • Tissue Extracts
  • cabozantinib
  • Phenylthiohydantoin
  • Bevacizumab
  • Denosumab
  • cabazitaxel
  • sipuleucel-T
  • enzalutamide
  • Prostate-Specific Antigen
  • abiraterone
  • Dasatinib
  • Atrasentan
  • Sunitinib

Associated data

  • ClinicalTrials.gov/NCT00861614
  • ClinicalTrials.gov/NCT01057810