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Cancer Biology Program, Hematology-Oncology Division (S.R.L., S.M.R., A.K., D.M., K.D.S., S.P.B.), Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; and Urology Division (M.L.L.), Department of Surgery, Brigham and Womens Hospital, Boston, Massachusetts 02115
Address all correspondence and requests for reprints to: Steven P. Balk, Hematology-Oncology Division, Beth Israel Deaconess Medical Center, HIM Building-Room 1050, 330 Brookline Avenue, Boston, Massachusetts 02215. E-mail sbalk{at}caregroup.harvard.edu
A human protein termed p21-activated kinase 6 (PAK6), based on
homology to the PAK family of serine/threonine kinases, was cloned as
an AR interacting protein. PAK6 was a 75-kDa protein with a predicted
N-terminal Cdc42/Rac interactive binding domain and a C-terminal
kinase domain. PAK6 bound strongly to GTP-Cdc42 and weakly to GTP-Rac.
In contrast to most PAKs, kinase activity was not stimulated by Cdc42
or Rac, but could be stimulated by AR binding. PAK6 interacted with the
intact AR in a mammalian one-hybrid assay and bound in
vitro, without ligand, to the hinge region between the AR DNA-
and ligand-binding domains. PAK6 also bound to the ER
, and binding
was enhanced by 4-hydroxytamoxifen. AR and ER
transcriptional
activities were inhibited by PAK6 in transient transfections with
episomal and integrated reporter genes. AR inhibition was not reversed
by transfection with an activated Cdc42 mutant, Cdc42V12, which by
itself also inhibited AR transactivation. Epitope-tagged PAK6 was
primarily cytoplasmic in the absence or presence of AR and hormone.
PAK6 transcripts were expressed most highly in brain and testis, with
lower levels in multiple tissues including prostate and breast. PAK6
interaction provides a mechanism for cross-talk between steroid hormone
receptors and Cdc42-mediated signal transduction pathways and could
contribute to the effects of tamoxifen in breast cancer and in other
tissues.
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