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Bypass pathway: when leukemia cells are deprived of Gln, the serine pathway upregulates the key serine enzymes phosphoglycerate dehydrogenase (PHGDH) and phosphoribosyltransferase (PSAT), leading to an increased demand for serine and exacerbation of serine dependence in leukemia cells [117]

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Furthermore, blockade of eotaxin-2 by monoclonal antibody attenuated NASH and fibrosis in NAFLD animal models, thus suggesting a potential therapeutic role of anti-CCL24 agents in MASLD [161]