LAUSR

Graphical abstract Figure. No Caption available. ABSTRACT Hypoxia is an important module in all solid tumours to promote angiogenesis, invasion and metastasis. Stabilization and subsequent nuclear localization of HIF‐1&agr; subunits result in the activation of tumour promoting target genes such as VEGF, MMPs, Flt‐1, Ang‐1 etc. which plays a pivotal role in adaptation of tumour cells to hypoxia. Increased HIF‐&agr; and its nuclear translocation have been correlated with pronounced angiogenesis, aggressive tumour growth and poor patient prognosis leading to current interest in HIF‐1&agr; as an anticancer drug target. Benzophenone‐1B ([4‐(1H‐benzimidazol‐2‐ylmethoxy)‐3,5‐dimethylphenyl]‐(4‐methoxyphenyl) methanone, or BP‐1B) is a new antineoplastic agent with potential angiopreventive effects. Current investigation reports the cellular biochemical modulation underlying BP‐1B cytotoxic/antiangiogenic effects. Experimental evidences postulate that BP‐1B exhibits the tumour specific cytotoxic actions against various cancer types with prolonged action. Moreover BP‐1B efficiently counteracts endothelial cell capillary formation in in‐vitro, in‐vivo non‐tumour and tumour angiogenic systems. Molecular signaling studies reveal that BP‐1B arrests nuclear translocation of HIF‐1&agr; devoid of p42/44 pathway under CoCl2 induced hypoxic conditions in various cancer cells thereby leading to abrogated HIF‐1&agr; dependent activation of VEGF‐A, Flt‐1, MMP‐2, MMP ‐9 and Ang‐1 angiogenic factors resulting in retarded cell migration and invasions. The in‐vitro results were reproducible in the reliable in‐vivo solid tumour model. Taken together, we conclude that BP‐1B impairs angiogenesis by blocking nuclear localization of HIF‐1&agr; which can be translated into a potent HIF‐1&agr; inhibitor.