57 Old Forge Rd.
Tuxedo, NY 10987
Progression of the cell cycle is tightly regulated in order to ensure that genetic integrity is maintained and genetic information is passed correctly to daughter cells. Extensive research over the past two decades has revealed the existence of important surveillance mechanisms (referred to as checkpoints) that regulate cell cycle progression. These checkpoints monitor specific cell cycle?related processes and block cell cycle progression until these processes are completed with high fidelity. Cancer results from damage to multiple genes controlling cell division or cell death. An underlying genetic instability is required for the generation of multiple lesions that are characteristic of cancer. Genetic instability could be manifested as alterations in chromosome number as well as translocations, deletions, and insertions. Aneuploidy is frequently present in many types of tumor cell. A loss of the spindle checkpoint function and the control of anaphase entry appear to be causes leading to gross aneuploidy, a condition from which cells with an advantage for tumor growth will be selected. Thus, studying the mechanism underlying cohesion of sister chromatids and centrioles has the potential for identifying new targets for rational designing of anti-cancer drugs. In addition, a better understanding of biochemical pathways controlling checkpoint-induced programmed cell death may help us to better therapeutically induce resistant tumor cells to undergo apoptosis. We have been studying the function of molecular components in cell cycle regulation and in suppression tumorigenesis. Our recent studies on the function of Plk1, BubR1, and Sgo1 reveal that these cell cycle checkpoint regulators play an important role in the maintenance of genomic stability and suppression of tumor formation. We have obtained a series of mice with ablation of checkpoint genes. We believe these mice will be excellent animal models with which the effect of environmental agents on cacinogenesis can be studied.
Ex-vivo expansion of nonhuman primate CD34+ cells by stem cell factor Sall4B
Shen, Bin; Zhang, Yu; Dai, Wei; Ma, Yupo; Jiang, Yongping. Ex-vivo expansion of nonhuman primate CD34+ cells by stem cell factor Sall4B. Stem cell research & therapy. 2016 Oct 20;7(1):152-152 (2280092)
Unmasking PTEN's nuclear functions
Dai, Wei. Unmasking PTEN's nuclear functions. Cell cycle. 2016 Oct 20;15(24):3341-3342 (2280082)
Systemic chromosome instability in Shugoshin-1 mice resulted in compromised glutathione pathway, activation of Wnt signaling and defects in immune system in the lung
Yamada, H Y; Kumar, G; Zhang, Y; Rubin, E; Lightfoot, S; Dai, W; Rao, C V. Systemic chromosome instability in Shugoshin-1 mice resulted in compromised glutathione pathway, activation of Wnt signaling and defects in immune system in the lung. Oncogenesis. 2016 Aug 15;5(8):e256-e256 e256 (2218832)
Effect of Hypoxia-regulated Plk3 On Human Limbal Stem Cell Differentiation
Wang, Ling; Gonzalez, Sheyla; Dai, Wei; Deng, Sophie; Lu, Luo. Effect of Hypoxia-regulated Plk3 On Human Limbal Stem Cell Differentiation. Journal of biological chemistry. 2016 Aug 05;291(32):16519-16529 (2136562)
Antagonizing pathways leading to differential dynamics in colon carcinogenesis in Shugoshin1 (Sgo1)-haploinsufficient chromosome instability model
Rao, Chinthalapally V; Sanghera, Saira; Zhang, Yuting; Biddick, Laura; Reddy, Arun; Lightfoot, Stan; Dai, Wei; Yamada, Hiroshi Y. Antagonizing pathways leading to differential dynamics in colon carcinogenesis in Shugoshin1 (Sgo1)-haploinsufficient chromosome instability model. Molecular carcinogenesis. 2016 May;55(5):600-610 (2098102)