Constitutive Hedgehog Signaling in Chondrosarcoma Up-Regulates Tumor Cell Proliferation
Oncogene Proteins
Patched Receptors
0301 basic medicine
Reverse Transcriptase Polymerase Chain Reaction
DNA Mutational Analysis
Chondrosarcoma
Parathyroid Hormone-Related Protein
Bone Neoplasms
Receptors, Cell Surface
Mice, SCID
Immunohistochemistry
3. Good health
Patched-1 Receptor
Mice
03 medical and health sciences
Organ Culture Techniques
Mice, Inbred NOD
Animals
Humans
Hedgehog Proteins
Polymorphism, Single-Stranded Conformational
Cell Proliferation
Hypolipidemic Agents
DOI:
10.2353/ajpath.2006.050001
Publication Date:
2007-03-16T19:36:39Z
AUTHORS (10)
ABSTRACT
Chondrosarcoma is a malignant cartilage tumor that may arise from benign precursor lesions, such as enchondromas. Some cases of multiple enchondromas are caused by a mutation that results in constitutive activation of Hedgehog-mediated signaling. We found that chondrosarcomas expressed high levels of the Hedgehog target genes PTCH1 and GLI1. Treatment with parathyroid hormone-related protein down-regulated Indian Hedgehog (IHH) expression in normal growth plates but not in chondrosarcoma or enchondroma organ cultures. Treatment of the chondrosarcoma organ cultures with Hedgehog protein increased cell proliferation rate, whereas addition of chemical inhibitors of Hedgehog signaling decreased the proliferation rate. Chondrosarcoma xenografts from 12 different human tumors were established in NOD-SCID mice. Treatment with triparanol, an inhibitor of Hedgehog signaling, resulted in a 60% decrease in tumor volume, a 30% decrease in cellularity, and a 20% reduction in proliferation rate. These results show that Hedgehog signaling is active in chondrosarcoma and benign cartilage tumors and regulates tumor cell proliferation. Our data raise the intriguing possibility that Hedgehog blockade could serve as an effective treatment for chondrosarcoma, a tumor for which there are currently no universally effective nonsurgical management options.
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