Two Isoforms of Ubiquitin Carboxyl-Terminal Hydrolase Isozyme L1 (UCH-L1) were Down-Regulated in High Metastatic Potential of Human SN12C Renal Cell Carcinoma Cell Clones
Two Isoforms of Ubiquitin Carboxyl-Terminal Hydrolase Isozyme L1 (UCH-L1) were Down-Regulated in High Metastatic Potential of Human SN12C Renal Cell Carcinoma Cell Clones
复制标题
泛素羧基末端水解酶同工酶 L1 (UCH-L1) 的两种亚型在人 SN12C 肾细胞癌细胞克隆的高转移潜能中下调
DOI:
10.4172/jpb.s1000158
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发表时间:
2008
期刊:
影响因子:
--
通讯作者:
Kazuyuki Nakamura
中科院分区:
文献类型:
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作者:
Toshiyuki Tanaka;Y. Kuramitsu;M. Fujimoto;S. Naito;M. Oka;Kazuyuki Nakamura
The SN12C renal cell carcinoma cell clones were parent cell line and 3 clones. SN12C parent cell line was established from a human renal cell carcinoma surgical specimen. The two clones, SN12C-clone 2 and SN12C-PM 6, have higher than the parent cell line. The SN12C-clone 4 has lower than the parent cell line. Using two-dimensional gel electrophoresis, we detected eight proteins showing differential spot intensity between parent cell line and high metastatic clones. And we have identified 5 out of the 8 proteins by using liquid chromatography-tandem mass spectrometry. We found two isoforms of UCH-L1 protein which was shown to be significantly down-regulated in the high metastatic clones. However, the mechanisms of down-regulation of UCH-L1 which were involved in metastasis still remain to be characterized. To clarify the mechanism of UCH-L1 protein expression, further studies will be necessary. Furthermore, we need to examine in what kind of integral mechanism does the down-regulation of UCH-L1 occur.