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The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants.

The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Research Abstract Details 

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  • The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Abstract Text:

    BACKGROUND: Oncogenic RAS mutants such as v-Ha-RAS activate members of Rac/CDC42-dependent kinases (PAKs) and appear to contribute to the development of more than 30% of all human cancers. PAK1 activation is essential for oncogenic RAS transformation, and several chemical compounds that inhibit Tyr kinases essential for the RAS-induced activation of PAK1 strongly suppress RAS transformation either in cell culture or in vivo (nude mice). Although we have developed a cell-permeable PAK-specific peptide inhibitor called WR-PA18, so far no chemical (metabolically stable) compound has been developed that directly inhibits PAK1 in a highly selective manner. Thus, we have explored such a PAK1 inhibitor(s) among synthetic derivatives of an adenosine triphosphate antagonist. RESULTS: From the naturally occurring adenosine triphosphate antagonist K252a, we have developed two bulky derivatives, called CEP-1347 and KT D606 (a K252a dimer), which selectively inhibit PAKs or mixed-lineage kinases both in vitro and in cell culture and convert v-Ha-RAS-transformed NIH 3T3 cells to flat fibroblasts similar to the parental normal cells. Furthermore, these two K252a analogues suppress the proliferation of v-Ha-RAS transformants, but not the normal cells. CONCLUSION: These bulky adenosine triphosphate antagonists derived from K252a or related indolocarbazole compounds such as staurosporine would be potentially useful for the treatment of RAS/ PAK1-induced cancers, once their anti-PAK1 activity is significantly potentiated by a few additional chemical modifications at the sugar ring suggested in this paper.

    The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Publishing Authors By Initials

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    PUBMED ID PMID:

    MEDLINE DATE: 2002 Jul-Aug

    The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Cancer journal (Sudbury, Mass.)

    VOLUME: 8

    Page Numbers: 328-36

    Journal Abbreviation:

    ISSN: 1528-9117

    DAY: 28

    MONTH: 06

    YEAR: 2008

    The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100931981

    The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Keywords Mesh Terms:

    KEYWORDS: Staurosporine

    MESH TERMS: chemistry

    Chemical & Substance for Abstract: The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants. Information

    Substance Name: mitogen-activated protein kinase kinase

    Registry Number: EC 2.7.11.25

    Grant and Affiliation Information for The K252a derivatives, inhibitors for the PAK/MLK kinase family selectively block the growth of RAS transformants.

    AFFILIATION: Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Parkville, Australia.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Cancer J

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