Glucokinase links metabolism and lineage plasticity in neuroendocrine prostate cancer via interaction with AKT1

Shen, K.; Su, R.; Ji, Y.; Zhang, W.; Liu, X.; Chai, X.; Wang, J.; Liu, B.; Li, A.; Wu, H.; Wang, T.; Zhou, X.; Jiang, Z.; Zhu, H. H.; Dong, L.; Zhu, Y.; Dong, B.; Pan, J.; Wang, Q.; Xue, W.

doi:10.64898/2026.01.06.697917

bioRxiv · 10.64898/2026.01.06.697917

Glucokinase links metabolism and lineage plasticity in neuroendocrine prostate cancer via interaction with AKT1

Shen, K.·Su, R.·Ji, Y.·Zhang, W.·Liu, X.·Chai, X.·Wang, J.·Liu, B.·Li, A.·Wu, H.·Wang, T.·Zhou, X.·Jiang, Z.·Zhu, H. H.·Dong, L.·Zhu, Y.·Dong, B.·Pan, J.·Wang, Q.·Xue, W.

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Abstract

Cancer cells frequently rewire their metabolism to sustain growth and survival under stress. Despite the critical role of metabolic adaptation in tumorigenesis, how specific metabolic enzymes regulate lineage plasticity remains unclear. Here, through FDG-PET imaging and transcriptomic analyses, we reveal markedly elevated glucose uptake in neuroendocrine prostate cancer (NEPC) and identify glucokinase (GCK) as a MYCN-induced metabolic enzyme. Beyond its metabolic role, GCK is indispensable for maintaining the neuroendocrine lineage of prostate cancer cells by establishing a functional circuit with AKT1 through reciprocal regulation--AKT1 binds and phosphorylates GCK at S373, whereas GCK phosphorylates AKT1 at S473. Pharmacological disruption of this AKT1-GCK axis suppresses tumor growth in NEPC mouse models and patient-derived xenografts. Altogether, our findings uncover both the metabolic and noncanonical kinase functions of GCK and establish the AKT1-GCK axis as a key link between metabolic reprogramming and neuroendocrine lineage transition in prostate cancer.

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Shen, K., Su, R., Ji, Y., Zhang, W., Liu, X., Chai, X., Wang, J., Liu, B., Li, A., Wu, H., Wang, T., Zhou, X., Jiang, Z., Zhu, H. H., Dong, L., Zhu, Y., Dong, B., Pan, J., Wang, Q., Xue, W.. 2026-01-07. Glucokinase links metabolism and lineage plasticity in neuroendocrine prostate cancer via interaction with AKT1. https://doi.org/10.64898/2026.01.06.697917

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