PURPOSE: This study aimed to explore the potential of sialic acid - related selectin targeting strategy in the treatment of leukemia and some solid tumors. We expected it could "actively" bind tumor cells and kill them, reducing non-specific toxicity to normal cells. METHODS: BOR-SA prodrug was synthesized by reacting an ortho-dihydroxy group in SA with a boronic acid group in BOR. Two kinds of leukemia cells (RAW264.7 and HL60 cells), one solid sarcoma cell model (S180 cells) and their corresponding normal cells (monocytes (MO), neutrophil (NE) and fibroblast (L929)) were selected for the in vitro cell experiments (cytotoxicity, cellular uptake, cell cycle and apoptosis experiments). The S180 tumor-bearing Kunming mice model was established for anti-tumor pharmacodynamic experiments. RESULTS: In vitro cell assay results showed that uptake of BOR-SA by HL60 and S180 cells were increased compared with the control group. BOR-SA induced a lower IC50, higher ratio of apoptosis and cell cycle arrest of tumor cells. In vivo anti-S180 tumor pharmacodynamics experiments showed that mice in the BOR-SA group had higher tumor inhibition rate, higher body weight and lower immune organ toxicity compared with the control group. CONCLUSIONS: sialic acid-mediated selectin targeting strategy may have great potential in the treatment of related tumors.
PURPOSE: This study aimed to explore the potential of sialic acid - related selectin targeting strategy in the treatment of leukemia and some solid tumors. We expected it could "actively" bind tumor cells and kill them, reducing non-specific toxicity to normal cells. METHODS:BOR-SA prodrug was synthesized by reacting an ortho-dihydroxy group in SA with a boronic acid group in BOR. Two kinds of leukemia cells (RAW264.7 and HL60 cells), one solid sarcoma cell model (S180 cells) and their corresponding normal cells (monocytes (MO), neutrophil (NE) and fibroblast (L929)) were selected for the in vitro cell experiments (cytotoxicity, cellular uptake, cell cycle and apoptosis experiments). The S180tumor-bearing Kunming mice model was established for anti-tumor pharmacodynamic experiments. RESULTS: In vitro cell assay results showed that uptake of BOR-SA by HL60 and S180 cells were increased compared with the control group. BOR-SA induced a lower IC50, higher ratio of apoptosis and cell cycle arrest of tumor cells. In vivo anti-S180tumor pharmacodynamics experiments showed that mice in the BOR-SA group had higher tumor inhibition rate, higher body weight and lower immune organ toxicity compared with the control group. CONCLUSIONS:sialic acid-mediated selectin targeting strategy may have great potential in the treatment of related tumors.
Authors: M P Albero; J M Vaquer; E J Andreu; J J Villanueva; L Franch; C Ivorra; E Poch; X Agirre; F Prosper; I Pérez-Roger Journal: Oncogene Date: 2010-03-22 Impact factor: 9.867
Authors: William Blum; Sebastian Schwind; Somayeh S Tarighat; Susan Geyer; Ann-Kathrin Eisfeld; Susan Whitman; Alison Walker; Rebecca Klisovic; John C Byrd; Ramasamy Santhanam; Hongyan Wang; John P Curfman; Steven M Devine; Samson Jacob; Celia Garr; Cheryl Kefauver; Danilo Perrotti; Kenneth K Chan; Clara D Bloomfield; Michael A Caligiuri; Michael R Grever; Ramiro Garzon; Guido Marcucci Journal: Blood Date: 2012-05-07 Impact factor: 22.113
Authors: Malin Wickström; Peter Nygren; Rolf Larsson; Johan Harmenberg; Jakob Lindberg; Per Sjöberg; Markus Jerling; Fredrik Lehmann; Paul Richardson; Kenneth Anderson; Dharminder Chauhan; Joachim Gullbo Journal: Oncotarget Date: 2017-06-08