Profiling and targeting cancer stem cell signaling pathways for cancer therapeutics
被引:14
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作者:
Borlongan, Mia C.
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Coll Grad Studies, Master Program Pharmaceut Sci, Elk Grove, CA 95758 USAColl Grad Studies, Master Program Pharmaceut Sci, Elk Grove, CA 95758 USA
Borlongan, Mia C.
[1
]
Wang, Hongbin
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机构:
Coll Grad Studies, Master Program Pharmaceut Sci, Elk Grove, CA 95758 USA
Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
Calif Northstate Univ, Dept Basic Sci, Coll Med, Elk Grove, CA 95757 USAColl Grad Studies, Master Program Pharmaceut Sci, Elk Grove, CA 95758 USA
Wang, Hongbin
[1
,2
,3
]
机构:
[1] Coll Grad Studies, Master Program Pharmaceut Sci, Elk Grove, CA 95758 USA
[2] Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
[3] Calif Northstate Univ, Dept Basic Sci, Coll Med, Elk Grove, CA 95757 USA
Tumorigenic cancer stem cells (CSCs) represent a subpopulation of cells within the tumor that express genetic and phenotypic profiles and signaling pathways distinct from the other tumor cells. CSCs have eluded many conventional antioncogenic treatments, resulting in metastases and relapses of cancers. Effectively targeting CSCs' unique self-renewal and differentiation properties would be a breakthrough in cancer therapy. A better characterization of the CSCs' unique signaling mechanisms will improve our understanding of the pathology and treatment of cancer. In this paper, we will discuss CSC origin, followed by an in-depth review of CSC-associated signaling pathways. Particular emphasis is given on CSC signaling pathways' ligand-receptor engagement, upstream and downstream mechanisms, and associated genes, and molecules. Signaling pathways associated with regulation of CSC development stand as potential targets of CSC therapy, which include Wnt, TGF beta (transforming growth factor-beta)/SMAD, Notch, JAK-STAT (Janus kinase-signal transducers and activators of transcription), Hedgehog (Hh), and vascular endothelial growth factor (VEGF). Lastly, we will also discuss milestone discoveries in CSC-based therapies, including pre-clinical and clinical studies featuring novel CSC signaling pathway cancer therapeutics. This review aims at generating innovative views on CSCs toward a better understanding of cancer pathology and treatment.
机构:
Queen Elizabeth Hosp, Dept Clin Oncol, Kowloon, Hong Kong, Peoples R ChinaQueen Elizabeth Hosp, Dept Clin Oncol, Kowloon, Hong Kong, Peoples R China
机构:
Univ Kansas, Med Ctr, Dept Surg, 3901 Rainbow Blvd,Mail Stop 3040, Kansas City, KS 66160 USAUniv Kansas, Med Ctr, Dept Surg, 3901 Rainbow Blvd,Mail Stop 3040, Kansas City, KS 66160 USA
Dandawate, Prasad R.
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Subramaniam, Dharmalingam
Jensen, Roy A.
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机构:
Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS 66160 USA
Univ Kansas, Med Ctr, Dept Pathol & Lab Med, Kansas City, KS 66160 USA
Univ Kansas, Med Ctr, Ctr Canc, Kansas City, KS 66160 USAUniv Kansas, Med Ctr, Dept Surg, 3901 Rainbow Blvd,Mail Stop 3040, Kansas City, KS 66160 USA
机构:
Brazilian Natl Canc Inst, Stem Cell Lab, Rio De Janeiro, RJ, BrazilBrazilian Natl Canc Inst, Stem Cell Lab, Rio De Janeiro, RJ, Brazil
Barreto Pires, Bruno Ricardo
Soares De Amorim, Isis Salviano
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机构:
Univ Estado Rio De Janeiro, Roberto Alcantara Gomes Biol Inst, Biophys & Biometry Dept, Rio De Janeiro, RJ, BrazilBrazilian Natl Canc Inst, Stem Cell Lab, Rio De Janeiro, RJ, Brazil
Soares De Amorim, Isis Salviano
Duarte E Souza, Layane
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机构:
Univ Estado Rio De Janeiro, Roberto Alcantara Gomes Biol Inst, Biophys & Biometry Dept, Rio De Janeiro, RJ, BrazilBrazilian Natl Canc Inst, Stem Cell Lab, Rio De Janeiro, RJ, Brazil
Duarte E Souza, Layane
Rodrigues, Juliana Alves
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机构:
Univ Estado Rio De Janeiro, Roberto Alcantara Gomes Biol Inst, Biophys & Biometry Dept, Rio De Janeiro, RJ, BrazilBrazilian Natl Canc Inst, Stem Cell Lab, Rio De Janeiro, RJ, Brazil
Rodrigues, Juliana Alves
Mencalha, Andre Luiz
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机构:
Univ Estado Rio De Janeiro, Roberto Alcantara Gomes Biol Inst, Biophys & Biometry Dept, Rio De Janeiro, RJ, BrazilBrazilian Natl Canc Inst, Stem Cell Lab, Rio De Janeiro, RJ, Brazil