期刊
ACTA PHARMACOLOGICA SINICA
卷 33, 期 2, 页码 250-260出版社
NATURE PUBL GROUP
DOI: 10.1038/aps.2011.163
关键词
human lung cancer cells; transducer of ErbB-2.1 (T0B1); PTEN; carcinogenesis; metastasis; RNA interference
资金
- Program for Changjiang Scholars and Innovative Research Team in University [IRT0849]
- National Natural Science Foundation of China [81071906]
- Ministry of Education of China [K512602110]
- College Nature Science Foundation of Jiangsu Province [SZ126821]
- Jiangsu Higher Education Institutions
Aim: To investigate the effects of the transducer of ErbB-2.1 (1081) on the proliferation, migration and invasion of human lung cancer cells in vitro. Methods: Human lung cancer cell lines (95-D, A549, NCl-H1299, NCl-H1975, NCl-H661, NCl-H446, NCl-H1395, and Calu-3) and the normal human bronchial epithelial (HBE) cell line were tested. The expression levels of TOB1 in the cells were determined with Western blot and RT-PCR analyses. TOB1-overexpressing cell line 95-D/TOB1 was constructed using lipofectamine-induced 1081 recombinant plasmid transfection and selective G418 cell culture. The A549 cells were transcend-transfected with TOB1-siRNA. MTT assay, flow cytometry and Western blot analysis were used to examine the effects of TOB1 on cancer cell proliferation and wound healing. Transwell invasive assay was performed to evaluate the effects of TOB1 on cancer cell migration and invasion. The activity of MMP2 and MMP9 was measured using gelatin zymography assay. Results: The expression levels of 1061 in the 8 human lung cancer cell lines were significantly lower than that in HBE cells. 1081 overexpression inhibited the proliferation of 95-D cells, whereas TOB1 knockdown with TOB1-sIRNA promoted the growth of A549 cells. Decreased cell migration and invasion were detected in 95-D/TOB1 cells, and the suppression of TOB1 enhanced the metastasis in A549 cells. TOB1 overexpression not only increased the expression of the phosphatase and tensin homolog (PTEN), an important tumor suppressor, but also regulated the downstream effectors in the PI3K/PTEN signaling pathway, including Akt, ERK1/2, etc. In contrast, decreased expression of 1081 oppositely regulated the expression of these factors. TOB1 also regulates the gelatinase activity of MMP2 and MMP9 in lung cancer cells. Conclusion: The results demonstrate that the PI3K/PTEN pathway, which is essential for carcinogenesis, angiogenesis, and metastasis, may be one of the possible signaling pathways for regulation of proliferation and metastasis of human lung cancer cells by TOB1 in vitro.
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