lithium-chloride and Medulloblastoma

lithium-chloride has been researched along with Medulloblastoma* in 2 studies

Other Studies

2 other study(ies) available for lithium-chloride and Medulloblastoma

ArticleYear
Wnt/β-catenin signaling inhibits the Shh pathway and impairs tumor growth in Shh-dependent medulloblastoma.
    Acta neuropathologica, 2014, Volume: 127, Issue:4

    Topics: Animals; beta Catenin; Cells, Cultured; Cerebellar Neoplasms; Green Fluorescent Proteins; Hedgehog Proteins; Humans; Ki-67 Antigen; Lithium Chloride; Medulloblastoma; Mice, Transgenic; Signal Transduction; Wnt Proteins

2014
Lithium induces mortality in medulloblastoma cell lines.
    International journal of oncology, 2010, Volume: 37, Issue:3

    Lithium is the main therapeutic agent for the treatment of bipolar disorders but nerve cells are not the sole target of this drug. Indeed, lithium has been reported to target numerous cell types and to affect cell proliferation, differentiation and death. Lithium targets a variety of enzymes among which there is GSK-3beta and a number of cell responses elicited by lithium are mediated by the Wnt pathway that is involved in medulloblastoma (MB) pathogenesis. We studied the in vitro effects of lithium on two different MB cell lines: D283MED and DAOY. High doses of lithium inhibited GSK3-beta, decreased cell proliferation and induced non-apoptotic cell death in both cell lines independently by intracellular levels of beta-catenin that is consistently high only in D283MED. At clinical doses, the anti-neoplastic effects were observed only in this cell line, highlighting the importance of a specific molecular background in determining the target therapy response. In conclusion, lithium could be a promising drug in MB, but an accurate molecular profile predictive of drug response still needs to be clarified.

    Topics: Cell Death; Cell Growth Processes; Cell Line, Tumor; Enzyme Activation; Genes, p53; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; Humans; Lithium Chloride; Medulloblastoma; Mutation; Wnt Proteins

2010