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The microtubule‐affinity regulating kinases (MARKs) family plays a crucial role in regulating breast cancer development and progression. However, its precise function and the relevant molecular mechanism in breast cancer have not yet been elucidated. In this study, analysis of The Cancer Genome Atlas (TCGA) data revealed that MARK2 expression was markedly upregulated in breast cancer tissues, and high expression of MARK2 was correlated with poor survival. Functional assays showed that MARK2 deletion or inhibition suppressed aerobic glycolysis and cell growth as well as induced cell cycle arrest and apoptosis in breast cancer cells. Mechanistically, MARK2 stimulates mTOR‐mediated hypoxia‐inducible factor 1 alpha (HIF‐1α) transcription activity and represses p53‐transcription activity in breast cancer cells. TCGA data revealed that MARK2 expression was positively correlated with mTOR, Raptor, S6K1, glucose transporter 1, lactate dehydrogenase, HIF‐1α, and 4E‐BP1 expression, whereas negatively correlated with p53, p21, and Bax in breast cancer tissue. Conclusively, our study demonstrated that MARK2 promotes breast cancer aerobic glycolysis and cell proliferation, and inhibits apoptosis, in part, through regulating mTOR/HIF‐1α and p53 signaling pathways. Overall, these findings point to the potential of targeting MARK2 for breast cancer treatment.

Pd(ii) chromone Schiff base complex catalysed the dehydrogenative coupling of diosgenin and the obtained derivatives induced apoptosis by inhibiting AKT1 signaling pathway in breast cancer cells.