Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/67951
標題: Zoledronic acid induces cell-cycle prolongation in murine lung cancer cells by perturbing cyclin and Ras expression
作者: Li, Y.Y.
Chang, J.W.C.
Liu, Y.C.
Wang, C.H.
Chang, H.J.
Tsai, M.C.
Su, S.P.
Yeh, K.Y.
關鍵字: cell cycle
cyclins
lung cancer
Ras protein
zoledronic acid
containing bisphosphonates inhibit
dependent kinase inhibitor
retinoblastoma protein
mevalonate pathway
tracheal myocytes
in-vitro
breast
growth
phosphorylation
prostate
期刊/報告no:: Anti-Cancer Drugs, Volume 22, Issue 1, Page(s) 89-98.
摘要: Zoledronic acid (ZOL) was shown earlier to prolong survival in animal models of lung cancer. The aim of this study was to examine whether alteration of intracellular cyclins, cyclin-dependent kinases, cyclin-dependent kinase inhibitors, retinoblastoma, and Ras protein expression and E2F localization are among the possible antilung cancer mechanisms driven by ZOL. Furthermore, we used geranylgeraniol to test whether the mevalonate pathway is involved in the antitumor effects of ZOL against lung cancer. Line-1 cells, a murine lung adenocarcinoma cell line, were examined. ZOL significantly slowed the growth of these cells both in vitro and in vivo. The ZOL-treated cells typically arrested at the S/G2/M phase of the cell cycle, accompanied by increased intracellular levels of cyclin A, B1, and CDC2 and decreased levels of cyclin D, p21, p27, phosphorylated retinoblastoma, and Ras. In addition, ZOL affected the distribution of E2F. When geranylgeraniol was added to the ZOL-treated cells, either in vitro or in vivo, tumor growth, cell-cycle progression, the expression of certain cyclins, and cyclin-related regulatory proteins were partially returned to that of untreated controls. Therefore, ZOL elicits cell-cycle prolongation that seems to be associated with alterations in the levels of certain cyclins and cyclin-related regulatory proteins. Furthermore, the mevalonate pathway regulates ZOL-induced murine lung cancer inhibition both in vitro and in vivo. Anti-Cancer Drugs 22:89-98 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
URI: http://hdl.handle.net/11455/67951
ISSN: 0959-4973
文章連結: http://dx.doi.org/10.1097/CAD.0b013e3283400a05
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