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Differential expression of a tropomyosin isoform in low- and high-metastatic Lewis lung carcinoma cells.
Author(s) -
Keizo Takenaga,
Yohko Nakamura,
S Sakiyama
Publication year - 1988
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.8.9.3934
Subject(s) - lewis lung carcinoma , biology , gene isoform , tropomyosin , metastatic carcinoma , cancer research , phenotype , incubation , microbiology and biotechnology , carcinoma , lung cancer , metastasis , medicine , biochemistry , cancer , gene , actin , genetics
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.

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