Takenaga K, Nakamura Y, Sakiyama S
Division of Chemotherapy, Chiba Cancer Center Research Institute, Japan.
Mol Cell Biol. 1988 Sep;8(9):3934-7. doi: 10.1128/mcb.8.9.3934-3937.1988.
Two-dimensional electrophoretograms of newly synthesized polypeptides from low-metastatic (P29) and high-metastatic (D6) Lewis lung carcinoma cells were compared. The results showed that the synthesis of tropomyosin 2 (TM2) was significantly less in D6 cells than in P29 cells. Furthermore, suppression of TM2 synthesis was induced in P29 cells during incubation in medium containing dimethyl sulfoxide or butyric acid, which induced the metastatic phenotype of P29 cells. These results suggest that the suppression of TM2 synthesis is linked to the metastatic potential of Lewis lung carcinoma cells.
比较了低转移性(P29)和高转移性(D6)Lewis肺癌细胞新合成多肽的二维电泳图谱。结果显示,原肌球蛋白2(TM2)在D6细胞中的合成显著少于P29细胞。此外,在含有二甲亚砜或丁酸的培养基中孵育期间,P29细胞中TM2的合成受到抑制,这诱导了P29细胞的转移表型。这些结果表明,TM2合成的抑制与Lewis肺癌细胞的转移潜能有关。