Uesugi Y, Fuse I, Toba K, Kishi K, Hashimoto S, Furukawa T, Narita M, Takahashi M, Aizawa Y
First Dept. of Internal Medicine, Niigata University School of Medicine, Niigata City, Japan.
J Exp Clin Cancer Res. 2000 Sep;19(3):363-6.
We previously reported that the expression and the activity of SHP-1, a non-transmembrane protein tyrosine phosphatase (PTPase) increased during myeloid differentiation of an acute promyelocytic leukemia cell line (HT93) induced by all-trans retinoic acid (ATRA). To examine whether inhibition of SHP-1 activity attenuates myeloid differentiation, we used a new PTPase inhibitor, 3,4-dephostatin, and studied its effect on myeloid differentiation. Suppressive effects on immunoprecipitated SHP-1 phosphatase activity and myeloid cell differentiation were detected. These results suggest that SHP-1 is a substrate for 3,4-dephostatin, and that SHP-1 PTPase activity is closely related to myeloid differentiation.