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By elucidating the role of PGC-1 in cancer metabolism, this study provides new insights into the molecular underpinnings of bladder cancer metastasis and offers potential avenues for developing targeted therapies aimed at the metabolic vulnerabilities of this malignancy
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However, the mainly difference is that the hydrophobic and hydrogen-bonding interactions contributed by the active site residues, H244, E256 and F264 in mushroom tyrosinase are not observed in the corresponding active site residues, P505, S515 and I523 of human tyrosinase (Supplementary Fig
First-in-human (FIH) clinical trials are the initial Phase 1 studies and thus pose significant challenges regarding their design and safety
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