Targeting the mammalian target of rapamycin in myxoid chondrosarcoma
Ofer Merimsky1, Rinat Bernstein-Molho, Ronit Sagi-Eisenberg
1Tel-Aviv Sourasky Medical Center, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. merimsky@zahav.net.il
Abstract:
Myxoid chondrosarcoma is a slow-growing sarcoma poorly responsive to chemotherapy and radiation therapy. Translational research has validated several proteins as optional therapeutic targets. Significant responses are, however, rare. In this paper we report an extraordinary response of myxoid chondrosarcoma to targeted therapy by rapamycin in combination with cyclophosphamide. Our case points to a possible novel therapeutic approach towards myxoid chondrosarcoma, by targeting the mammalian target of rapamycin protein, and probably protein kinase C-alpha, mitogen-activated protein kinase, and Jun N-terminal kinase too, by rapamycin.
Insights
An extraordinary response in myxoid chondrosarcoma was observed with targeted therapy. Rapamycin combined with cyclophosphamide shows promise for this rare, slow-growing sarcoma.
Area of Science:
- Oncology
- Pharmacology
Background:
- Myxoid chondrosarcoma is a rare, slow-growing bone cancer.
- It exhibits poor responsiveness to conventional chemotherapy and radiation therapy.
- Targeted protein therapies are being explored for this challenging condition.
Observation:
- A patient with myxoid chondrosarcoma experienced an exceptional response to treatment.
- The therapy involved rapamycin in combination with cyclophosphamide.
Findings:
- This combination therapy demonstrated significant efficacy in a patient with myxoid chondrosarcoma.
- Rapamycin targets the mammalian target of rapamycin (mTOR) pathway.
Implications:
- This case suggests a potential novel therapeutic strategy for myxoid chondrosarcoma.
- Targeting mTOR, protein kinase C-alpha, mitogen-activated protein kinase, and Jun N-terminal kinase may be beneficial.
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