
Cancer Cell International, Journal Year: 2024, Volume and Issue: 24(1)
Published: Dec. 18, 2024
Language: Английский
Cancer Cell International, Journal Year: 2024, Volume and Issue: 24(1)
Published: Dec. 18, 2024
Language: Английский
Biomedicines, Journal Year: 2024, Volume and Issue: 12(10), P. 2211 - 2211
Published: Sept. 27, 2024
: N
Language: Английский
Citations
1Cancers, Journal Year: 2024, Volume and Issue: 16(17), P. 3031 - 3031
Published: Aug. 30, 2024
Background: mTORC1 activity is dependent on the presence of micronutrients, including Asparagine (Asn), to promote anabolic cell signaling in many cancers. We hypothesized that targeting Asn metabolism would inhibit tumor growth by reducing well-differentiated (WD)/dedifferentiated (DD) liposarcoma (LPS). Methods: Human metabolomic analysis was utilized compare abundance WD vs. DD LPS. Gene set enrichment (GSEA) compared relative expression among metabolic pathways upregulated Proliferation assays were performed for LPS lines and organoid models using combination treatment electron transport chain (ETC) inhibitors with Asn-free media. 13C-Glucose-labeling metabolomics evaluated effects nucleotide synthesis. Murine xenograft used assess ETC inhibition combined PEGylated L-Asparaginase (PEG-Asnase) signaling. Results: enriched GSEA indicated Within available models, media resulted reduced proliferation. Combination inhibited synthesis promoted cycle arrest. In vivo, PEG-Asnase restricted growth. Conclusions: upregulation are important factors contributing WD/DD progression. Effective strategies require limiting access extracellular de novo mechanisms. The an effective therapy restrict
Language: Английский
Citations
1Cancer Cell International, Journal Year: 2024, Volume and Issue: 24(1)
Published: Dec. 18, 2024
Language: Английский
Citations
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