TY - JOUR
T1 - Cancer stem cells in colorectal cancer from pathogenesis to therapy: controversies and perspectives
AU - Fanali, Caterina
AU - Lucchetti, Donatella
AU - Farina, Marisa
AU - Corbi, Maddalena
AU - Cufino, Valerio
AU - Cittadini, Achille Renato Maria
AU - Sgambato, Alessandro
PY - 2014
Y1 - 2014
N2 - Colorectal cancer remains one of the most common and lethal malignancies worldwide despite the use of various therapeutic strategies. A better understanding of the mechanisms responsible for tumor initiation and progression is essential for the development of novel, more powerful therapies. The traditional, so-called "stochastic model" of tumor development, which assumes that each cancer cell is tumorigenic, has been deeply challenged during the past decade by the identification of cancer stem cells (CSCs), a biologically distinct subset of cells within the bulk of tumor mass. This discovery led to the development of the hierarchical model of tumorigenesis which assumes that only CSCs have the ability to initiate tumor growth, both at primary and metastatic sites. This model implies that the elimination of all CSCs is fundamental to eradicate tumors and that failure to do so might be responsible for the occurrence of relapses and/or metastases frequently observed in the clinical management of colorectal cancer patients. Identification and isolation of CSCs is essential for a better understanding of their role in the tumorigenetic process and for the development of CSC-specific therapies. Several methods have been used for this purpose and many efforts have been focused on the identification of specific CSC-surface markers. This review provides an overview of the proposed roles of CSC in human colorectal tumorigenesis focusing on the most important molecules identified as CSC-specific markers in colorectal cancer and on the potential strategies for the development of CSC-targeted therapy.
AB - Colorectal cancer remains one of the most common and lethal malignancies worldwide despite the use of various therapeutic strategies. A better understanding of the mechanisms responsible for tumor initiation and progression is essential for the development of novel, more powerful therapies. The traditional, so-called "stochastic model" of tumor development, which assumes that each cancer cell is tumorigenic, has been deeply challenged during the past decade by the identification of cancer stem cells (CSCs), a biologically distinct subset of cells within the bulk of tumor mass. This discovery led to the development of the hierarchical model of tumorigenesis which assumes that only CSCs have the ability to initiate tumor growth, both at primary and metastatic sites. This model implies that the elimination of all CSCs is fundamental to eradicate tumors and that failure to do so might be responsible for the occurrence of relapses and/or metastases frequently observed in the clinical management of colorectal cancer patients. Identification and isolation of CSCs is essential for a better understanding of their role in the tumorigenetic process and for the development of CSC-specific therapies. Several methods have been used for this purpose and many efforts have been focused on the identification of specific CSC-surface markers. This review provides an overview of the proposed roles of CSC in human colorectal tumorigenesis focusing on the most important molecules identified as CSC-specific markers in colorectal cancer and on the potential strategies for the development of CSC-targeted therapy.
KW - Animals
KW - Antineoplastic Agents
KW - Cancer stem cells
KW - Cancer therapy
KW - Colorectal Neoplasms
KW - Colorectal cancer
KW - Humans
KW - Molecular Targeted Therapy
KW - Neoplastic Stem Cells
KW - Prognosis
KW - Prognostic marker
KW - Signal Transduction
KW - Tumor Markers, Biological
KW - Tumorigenesis
KW - Animals
KW - Antineoplastic Agents
KW - Cancer stem cells
KW - Cancer therapy
KW - Colorectal Neoplasms
KW - Colorectal cancer
KW - Humans
KW - Molecular Targeted Therapy
KW - Neoplastic Stem Cells
KW - Prognosis
KW - Prognostic marker
KW - Signal Transduction
KW - Tumor Markers, Biological
KW - Tumorigenesis
UR - http://hdl.handle.net/10807/125997
U2 - 10.3748/wjg.v20.i4.923
DO - 10.3748/wjg.v20.i4.923
M3 - Article
SN - 1007-9327
VL - 20
SP - 923
EP - 942
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
ER -