To explain the general tendency of large mothers to produce large offspring, we developed two models in which either the rate at which each single offspring extracts resources from the mother or the rate at which the mother supplies resources to all the offspring is limited (terminal- or upper-stream-limitation on resource transport, respectively). We also reanalyzed the data of Erythronium japonicum to test the models. The terminal-stream-limitation model predicted that the optimal offspring size that maximizes the fitness of the mother increases with an increase in the maximum rate of resource extraction by each single offspring. Thus, large mothers produce large offspring if the maximum resource extraction rate is high in those mothers. The upper-stream-limitation model predicted that the optimal offspring size decreases with an increase in the maximum rate of resource supply by the mother to all the offspring. In E. japonicum, the maximum growth rate of a seed was independent of the number of seeds of a plant, suggesting that the resource extraction rate is limited at the individual seed level. The maximum growth rate was high in large plants and had a strong positive effect on final seed mass. Thus, the results were consistent with the terminal-stream-limitation model.

These results suggest that dysregulation of ras is involved in at least 20% of ICC and expression of p53 protein is more significantly involved in ICC, particularly in the well and moderately differentiated cases. While some cases of p53 expression may be explainable by point mutation of p53, there may be some epigenetic phenomena that stabilize p53 protein in ICC. That is, wild type p53 may be stabilized and then detectable by forming complexes with other molecules of p53 downstream effector genes, such as WAF-1 and mdm-2.

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Abstract. Cepharanthine is a biscoclaurine alkaloid extracted from Stephania cepharantha Hayata, which is widely used for the treatment of many acute and chronic diseases, and can exert antitumor effects on several human cancer cell lines. However, little is known about the detailed mechanisms of the antitumor activity of Cepharanthine. In the present study, we determined whether Cepharanthine could suppress angiogenesis and growth of human oral squamous cell carcinoma (OSCC) cells in vitro and in vivo. Cepharanthine significantly inhibited expression of two major pro-angiogenic molecules, vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8), in cultured cells and in cells implanted into the subcutaneous tissue of nude mice. Also, Cepharanthine inhibited the nuclear factor-κB (NF-κB) activity in human OSCC cells in vitro and in vivo. The decreased expression of VEGF and IL-8 correlated with decreased tumor cell growth and decreased vascularization in vitro and in vivo. These findings suggest that Cepharanthine can suppress angiogenesis and growth of OSCC cells by inhibiting expression of VEGF and IL-8 involved in the blockade of NF-κB activity.