Survivin is a recently described inhibitor of apoptosis. Because suppression of apoptosis is important for carcinogenesis and tumor growth, we investigated the expression and function of survivin in human hepatocellular carcinomas (HCCs). We have shown that 4 HCC cell lines and 7 out of 8 human HCC tissues expressed survivin messenger RNA (mRNA), whereas expression of survivin mRNA was not detected in normal liver and nontumor areas of these tissues using the reverse transcription polymerase chain reaction. Survivin was detected primarily in the nucleus by immunofluorescence staining of HCC cells. In addition, 14 of 20 (70%) HCC tissues showed positive nuclear staining for survivin, whereas nontumor tissues showed little detectable staining by immunohistochemistry. Survivin expression strongly correlated with the proliferation index but not significantly with the apoptosis index in HCC tissues. Therefore, we performed cell cycle analysis after survivin transfection and showed that overexpression of survivin resulted in a decrease in the G 0 /G 1 phase and an increase in the S phase in all 4 HCC cell lines. Furthermore, we have found that survivin interacted with cyclin-dependent kinase 4 (Cdk4) and overexpression of survivin released p21 WAF1/Cip1 (p21) from Cdk4. From these results, we conclude that survivin promotes cell proliferation by interacting with Cdk4 and releasing p21 from Cdk4. This may play an important role in carcinogenesis and progression of human HCCs. (HEPA-TOLOGY 2000;31:1080-1085.)Regulation of programmed cell death is important in the preservation of homeostasis and morphogenesis of human tissues. 1,2 Impairment of apoptosis facilitates the accumulation of gene mutations by prolonging the cell cycle span and promoting resistance to immune-based cytotoxicity, 3 finally contributing to carcinogenesis. 4 It has been shown recently that the inhibitors of apoptosis proteins (IAP) are crucial regulators in the molecular mechanism of apoptosis. [5][6][7] Among the IAP members, survivin is unique in that it is undetectable in normal adult tissue, but abundantly expressed in transformed cells and a variety of human cancers. 8 It has also been shown that survivin inhibits apoptosis in cells exposed to diverse apoptotic stimuli 8-11 by associating with microtubules of the mitotic spindle 9 and inhibiting caspase activity. 10 Expression of survivin is highly correlated with prognosis in patients with neuroblastoma, 7,12 gastric cancer, 13 colorectal cancer, 14 and bladder cancers. 15 However, the biological functions of survivin, other than its antiapoptotic effect, are not well understood in human cancers.Therefore, to gain insight into additional roles of survivin in malignant cells, we investigated the expression and function of survivin in hepatocellular carcinoma (HCC) cell lines and human HCC. In this study, we showed that survivin expression correlates with HCC cell proliferation in the majority of human HCC tissues. Survivin overexpression obliterates the G 1 checkpoint by releasing p21 WAF1/Cip...

Phosphorylation of CPI-17 by Rho-associated kinase (Rho-kinase) and its effect on myosin phosphatase (MP) activity were investigated. CPI-17 was phosphorylated by Rho-kinase to 0.92 mol of P/mol of CPI-17 in vitro. The inhibitory phosphorylation site was Thr 38 (as reported previously) and was identified using a point mutant of CPI-17 and a phosphorylation state-specific antibody. Phosphorylation by Rho-kinase dramatically increased the inhibitory effect of CPI-17 on MP activity. Thus, CPI-17 as a substrate of Rho-kinase could be involved in the Ca 2 sensitization of smooth muscle contraction as a downstream effector of Rho-kinase. ß

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