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Vol. 58, Issue 6, 1287-1293, December 2000
Gastrointestinal Oncology Research Laboratory for New Drug
Development, Division of Solid Tumor Oncology, Department of
Medicine (X.-K.L., M.M., G.K.S.), Pharmacology and
Analytical Core Laboratory (W.T.), and Organic Synthesis Core
Laboratory (W.B.), Memorial Sloan-Kettering Cancer Center,
New York, New York
Huanglian is an herb that is widely used in China for the
treatment of gastroenteritis. We elected to determine whether huanglian could inhibit tumor cell growth by modulating molecular events directly
associated with the cell cycle. Huanglian inhibited tumor growth and
colony formation of gastric, colon, and breast cancer cell lines in a
time- and dose-dependent manner. Cell growth was completely inhibited
after 3 days of continuous drug exposure to 10 µg/ml of herb. This
degree of growth inhibition was significantly greater than that
observed with berberine, the major constituent of the herb. The
inhibition of cell growth by huanglian was associated with up to 8-fold
suppression of cyclin B1 protein. This resulted in complete inhibition
of cdc2 kinase activity and accumulation of cells in G2.
The mRNA expression of cyclin B1 was not changed after huanglian
treatment. There was no change in the protein expression of cyclins A
or E. Therefore, the effect of huanglian on inhibiting tumor growth
seems to be mediated by the selective suppression of cyclin B1, which
results in the inhibition of cdc2 kinase activity. Inhibition of cyclin
dependent kinase (cdk) activity is emerging as an attractive target for
cancer chemotherapy. Huanglian represents a class of agents that can
inhibit tumor cell growth by directly suppressing the expression of a
cyclin subunit that is critical for cell cycle progression. These
results indicate that traditional Chinese herbs may represent a new
source of agents designed for selective inhibition of cyclin dependent
kinases in cancer therapy.