Multi-omics analysis reveals that BUB1B is a cell cycle related gene promotes the bladder cancer development

Bladder cancer (BC) is characterized by a high incidence and frequent recurrence. Despite efforts to improve survival and reduce mortality among BC patients, significant progress remains elusive. The role of the cell cycle in BC has been increasingly studied, and our analysis revealed that BC exhibits elevated expression of BUB1 mitotic checkpoint serine/threonine kinase B (BUB1B). However, the role of BUB1B in BC remains not fully understood. A Multi-omics analysis was performed by integrating BUB1B expression with clinical data, and the results indicated that the upregulation of BUB1B was associated with poor prognosis. Moreover, our study demonstrated that BUB1B promotes bladder cancer (BC) cell proliferation, migration, invasion, and tumorigenicity both in vitro and in vivo . Finally, sequencing results revealed that overexpression of BUB1B resulted in the reduction of certain chemokines and was positively correlated with cell cycle-related proteins. These findings provided insights into the potential role of BUB1B as a therapeutic target for BC.