Research Topics | Masaaki HamaguchiSummaryAffiliation: Cold Spring Harbor Laboratory Country: USA Publications
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Publications
DBC2, a candidate for a tumor suppressor gene involved in breast cancerMasaaki Hamaguchi
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA
Proc Natl Acad Sci U S A 99:13647-52. 2002..By contrast, expression of a somatic mutant discovered in a breast cancer specimen does not suppress the growth of breast cancer cells...
DBC2 significantly influences cell-cycle, apoptosis, cytoskeleton and membrane-trafficking pathwaysVeeraiah Siripurapu
Cold Spring Harbor Laboratory, One Bungtown Road, Cold Spring Harbor, NY 11724, USA
J Mol Biol 346:83-9. 2005..The other network is related to cytoskeleton and membrane trafficking. Our findings suggest that the biological roles of DBC2 are related directly and/or indirectly to these cellular machineries...
DBC2 is essential for transporting vesicular stomatitis virus glycoproteinFaith K Chang
Department of Biological Sciences, Fordham University, 441 E Fordham Road, Bronx, NY 10458, USA
J Mol Biol 364:302-8. 2006..We demonstrate that DBC2 mobility depends also on an intact microtubule network. We conclude that DBC2 plays an essential role in microtubule-mediated VSVG transport from the endoplasmic reticulum to the Golgi apparatus...
Cyclin D1 down-regulation is essential for DBC2's tumor suppressor functionTakashi Yoshihara
Department of Biological Sciences, Fordham University, 441 E Fordham Road, Larkin Hall, Bronx, NY 10458, USA
Biochem Biophys Res Commun 358:1076-9. 2007..Our results indicate that the down-regulation of CCND1 is an essential step for DBC2's growth suppression of cancer cells. We believe that this discovery contributes to a better understanding of DBC2's tumor suppressor function...
DBC2 resistance is achieved by enhancing 26S proteasome-mediated protein degradationDenise Collado
Department of Biological Sciences, Fordham University, 441 E Fordham Road, Larkin Hall, Bronx, NY 10458, USA
Biochem Biophys Res Commun 360:600-3. 2007..These findings indicate that the resistant T-47D cells survive DBC2 induction by rapid destruction of DBC2 through 26S proteasome-mediated protein degradation...
