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10 Conclusion and future perspectives The immunometabolic crosstalk between tumor-associated macrophages (TAMs) and ferroptotic cancer cells has emerged as a defining regulator of tumor fate, influencing progression, metastasis, immune evasion, and therapeutic response

The coding sequence was cloned into the pET-32a (+) plasmid vector through insertion between the XbaI and NotI

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Medication Interference Detail: Some drugs (e.g., valproic acid and certain antibiotics) can disrupt normal L-Carnitine metabolism and absorption