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Oral administration of muscle derived small molecules inhibits tumor spread while promoting normal cell growth in
S Bar-Yehuda1, T Farbstein, F Barer
1Laboratory of Clinical and Tumor Immunology, The Felsenstein Medical Research Center, Tel-Aviv University, Rabin Medical Center, Petach-Tikva, Israel.
Abstract:
Tumor metastases are extremely rare in striated muscles. This is surprising given the fact that this tissue constitutes 60% of body weight. The present study focuses on small molecules produced and secreted by muscle cells which possess anti-cancer activity in vivo. Recently we have shown that a low molecular weight fraction (< 1000 Dalton) of skeletal muscle cell conditioned medium (muscle factor-MF), markedly inhibits the proliferation of carcinoma, sarcoma or melanoma cell lines in vitro. The MF exerts a cytostatic effect on tumor cell growth and arrests the cells in the G0/G1 of the cell cycle. However, normal cell proliferation, such as bone marrow and fibroblasts, was stimulated following incubation with MF. In this study, the effect of orally administered MF on melanoma and sarcoma growth was examined in mice. The administration of MF to mice inoculated intravenously with melanoma (B16-F10) or sarcoma (MCA-105) cells, resulted in a statistically significant inhibition of metastatic lung foci. In a different model, melanoma was induced in the foot pad and after development of a local lesion, the leg was amputated. A prolonged survival time was observed in the MF treated groups. Since the MF stimulated bone marrow cell proliferation in vitro, we decided to test its efficacy as an inhibitor of the myelotoxic effect exerted by chemotherapy, in vivo. MF, administered after chemotherapy, restored the number of white blood cells and yielded an increased percentage of neutrophils compared with the decline in these parameters after administration of chemotherapy alone. Thus, it is indicated that MF exerted a systemic anti tumor and chemoprotective effect when given orally. It can be concluded that it is bioavailable and is not biodegradable in the digestive system. MF may be considered as a potential therapy for the prevention of tumor spread.
Insights
Muscle cells secrete a factor that inhibits tumor growth and spread. This muscle factor (MF) shows anti-cancer effects in mice and protects against chemotherapy side effects, suggesting potential for cancer prevention.
Area of Science:
- Oncology
- Cell Biology
- Pharmacology
Background:
- Tumor metastases are rare in striated muscle, despite its large body mass.
- Skeletal muscle cells produce small molecules with potential anti-cancer properties.
- A low molecular weight fraction of conditioned muscle medium (muscle factor, MF) inhibits tumor cell proliferation in vitro.
Purpose of the Study:
- To investigate the in vivo anti-cancer and chemoprotective effects of orally administered muscle factor (MF).
- To evaluate MF's efficacy in preventing tumor metastasis and prolonging survival.
- To assess MF's ability to counteract chemotherapy-induced myelotoxicity.
Main Methods:
- Oral administration of MF to mice with melanoma or sarcoma.
- Intravenous inoculation of tumor cells to assess inhibition of lung metastases.
- Amputation model for local melanoma lesions to evaluate survival.
- Administration of MF post-chemotherapy to assess white blood cell recovery.
Main Results:
- MF significantly inhibited lung metastatic foci in mice with melanoma and sarcoma.
- MF administration prolonged survival time in mice with local melanoma lesions.
- MF restored white blood cell counts and increased neutrophil percentages after chemotherapy.
Conclusions:
- Orally administered MF exhibits systemic anti-tumor and chemoprotective effects.
- MF is bioavailable and resistant to degradation in the digestive system.
- Muscle factor (MF) represents a potential therapeutic agent for preventing tumor metastasis and mitigating chemotherapy side effects.

