British journal of pharmacology · 2026
Therapeutic targeting of GSK-3β activation by the tyrosine kinase RYK in pancreatic ductal adenocarcinoma with BJ-2412, a novel sunitinib analogue.
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Yadav Kiran, Chaudhary Prakash, Ghimire Kalpana, Mishra Sunil, Lee Hyunji, Bae Dawon, Chang Jae-Hoon, Jeong Byeong-Seon, Kim Jung-Ae
Аннотация
BACKGROUND AND PURPOSE: Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal malignancy with limited treatment options. RYK, an atypical receptor-like tyrosine kinase, has emerged as a potential regulator of tumour signalling, but its role in PDAC remains poorly understood. This study aimed to evaluate the anticancer potential of BJ-2412, a novel sunitinib analogue with RYK-inhibitory activity, and to elucidate the functional relevance of RYK in PDAC.
EXPERIMENTAL APPROACH: BJ-2412 was synthesized by introducing a 2,4-dimethylpyridin-3-ol moiety into sunitinib. Its anticancer activity was assessed in PDAC cell lines and mouse tumour models. Mechanistic studies included RTK phosphorylation profiling, RYK knockdown via siRNA, co-immunoprecipitation, immunoblotting of downstream effectors, and analyses of apoptosis, invasion, and macrophage phenotypes.
KEY RESULTS: BJ-2412 inhibited RYK phosphorylation by disrupting its interaction with EGFR. While RYK knockdown and BJ-2412 had minimal effects on proliferation, both impaired cancer cell survival, including that of cancer stem cells. We identified RYK as a GSK-3β activator that antagonizes canonical WNT signalling and RTK-mediated GSK-3β inhibition. BJ-2412 inactivated GSK-3β and reduced Sonic Hedgehog (Shh) and GLI1 expression. BJ-2412-induced up-regulation of WNT5A, cancer cell-selective apoptosis, M1-macrophage polarization, as well as down-regulation of MMPs and CTSS, were reversed by recombinant Shh. Finally, BJ-2412 suppressed tumour growth, invasion, and metastasis in xenograft and allograft mouse models.
CONCLUSIONS AND IMPLICATIONS: These findings identify RYK as a GSK-3β activator and a therapeutic vulnerability in PDAC. BJ-2412 demonstrates therapeutic potential by targeting this pathway and remodelling the tumour microenvironment, offering a multifaceted strategy against PDAC progression and resistance.
EXPERIMENTAL APPROACH: BJ-2412 was synthesized by introducing a 2,4-dimethylpyridin-3-ol moiety into sunitinib. Its anticancer activity was assessed in PDAC cell lines and mouse tumour models. Mechanistic studies included RTK phosphorylation profiling, RYK knockdown via siRNA, co-immunoprecipitation, immunoblotting of downstream effectors, and analyses of apoptosis, invasion, and macrophage phenotypes.
KEY RESULTS: BJ-2412 inhibited RYK phosphorylation by disrupting its interaction with EGFR. While RYK knockdown and BJ-2412 had minimal effects on proliferation, both impaired cancer cell survival, including that of cancer stem cells. We identified RYK as a GSK-3β activator that antagonizes canonical WNT signalling and RTK-mediated GSK-3β inhibition. BJ-2412 inactivated GSK-3β and reduced Sonic Hedgehog (Shh) and GLI1 expression. BJ-2412-induced up-regulation of WNT5A, cancer cell-selective apoptosis, M1-macrophage polarization, as well as down-regulation of MMPs and CTSS, were reversed by recombinant Shh. Finally, BJ-2412 suppressed tumour growth, invasion, and metastasis in xenograft and allograft mouse models.
CONCLUSIONS AND IMPLICATIONS: These findings identify RYK as a GSK-3β activator and a therapeutic vulnerability in PDAC. BJ-2412 demonstrates therapeutic potential by targeting this pathway and remodelling the tumour microenvironment, offering a multifaceted strategy against PDAC progression and resistance.