| Literature DB >> 22443277 |
Alice Zoccoli1, Michele Iuliani, Francesco Pantano, Marco Imperatori, Salvatore Intagliata, Bruno Vincenzi, Paolo Marchetti, Nicola Papapietro, Vincenzo Denaro, Giuseppe Tonini, Daniele Santini.
Abstract
INTRODUCTION: Bone marrow-derived cells (BMDC) localize in premetastatic niche through chemokines and integrins signals and establish clusters that precede the arrival of even single metastatic tumor cell at distant site. CSCs demonstrate an increased metastatic propensity and would seem likely candidates for the acquisition of migratory capabilities and propagation of heterogeneous tumor cell populations to different target organs. Sonic Hedgehog (SHH), FOXM1 and Notch pathways and signaling molecules such as integrin and chemokine could dictate their fate. AREAS COVERED: In this review, the molecular mechanisms of premetastatic niche onset are summarized. EXPERT OPINION: Premetastatic niche is defined as a fertile microenvironment that forms in metastatic target organ and facilitates the invasion, survival and/or proliferation of metastatic tumor cells, providing a novel mechanism for the promotion of metastasis. Drugs targeting premetastatic niche could represent a new promising therapeutic approach in the treatment of bone metastases.Entities:
Mesh:
Year: 2012 PMID: 22443277 DOI: 10.1517/14728222.2012.656092
Source DB: PubMed Journal: Expert Opin Ther Targets ISSN: 1472-8222 Impact factor: 6.902