Lemongrass essential oil and citral inhibit Src/Stat3 activity and suppress the proliferation/survival of small-cell lung cancer cells, alone or in combination with chemotherapeutic agents
URI | http://shark.lib.kagawa-u.ac.jp/kuir/metadata/28485 | ||||||
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Title |
Lemongrass essential oil and citral inhibit Src/Stat3 activity and suppress the proliferation/survival of small-cell lung cancer cells, alone or in combination with chemotherapeutic agents
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Description |
Abstract Small-cell lung cancer (SCLC) is intractable due to its high propensity for relapse. Novel agents are thus needed for SCLC treatment. Lemongrass essential oil (LG-EO) and its major constituent, citral, have been reported to inhibit the proliferation and survival of several types of cancer cells. However, the precise mechanisms through which LG-EO and citral exert their effects on SCLC cells have not been fully elucidated. SCLC cells express Src and have high levels of Src-tyrosine kinase (Src-TK) activity. In most SCLC cell lines, constitutive phosphorylation of Stat3(Y705), which is essential for its activation, has been detected. Src-TK can phosphorylate Stat3(Y705), and activated Stat3 promotes the expression of the anti-apoptotic factors Bcl-xL and Mcl-1. In the present study, LG-EO and citral prevented Src-TK from phosphorylating Stat3(Y705), resulting in decreased Bcl-xL and Mcl-1 expression, in turn suppressing the proliferation/survival of SCLC cells. To confirm these findings, the wild-type-src gene was transfected into the LU135 SCLC cell line (LU135‑wt-src), in which Src and activated phospho-Stat3(Y705) were overexpressed. The suppression of cell proliferation and the induction of apoptosis by treatment with LG-EO or citral were significantly attenuated in the LU135-wt-src cells compared with the control LU135-mock cells. The signal transducer and activator of transcription 3 (Stat3) signaling pathway is also associated with intrinsic drug resistance. LU135-wt-src cells were significantly resistant to conventional chemotherapeutic agents compared with LU135-mock cells. The combined effects of citral and each conventional chemotherapeutic agent on SCLC cells were also evaluated. The combination treatment exerted additive or more prominent effects on LU135-wt-src, LU165 and MN1112 cells, which are relatively chemoresistant SCLC cells. These findings suggest that either LG-EO or citral, alone or in combination with chemotherapeutic agents, may be a novel therapeutic option for SCLC patients. (医博甲693) |
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Publication Title |
International Journal of Oncology
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Publication Title Alternative |
Int J Oncol.
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Volume |
52
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Issue |
5
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Start Page |
1738
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End Page |
1748
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Publisher |
Spandidos Publications
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Published Date |
2018-03-13
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ISSN |
1019-6439
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NCID |
AA10992511
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PMID |
29568932
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DOI |
10.3892/ijo.2018.4314
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Resource Type |
Thesis or Dissertation
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Language |
eng
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Resource URL |
出版社盤DOIリンク(URL) : https://doi.org/10.3892/ijo.2018.4314
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Rights |
Copyright © Spandidos Publications 2018.
"This is the Publisher's version of the following article:Lemongrass essential oil and citral inhibit Src/Stat3 activity and suppress the proliferation/survival of small-cell lung cancer cells, alone or in combination with chemotherapeutic agents.; International Journal of Oncology; Volume 52 Issue 5 (2018)1738-1748; doi: 10.3892/ijo.2018.4314 , which has been published in final form at https://doi.org/10.3892/ijo.2018.4314 ."
DOI: https://doi.org/10.3892/ijo.2018.4314
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Text Version |
ETD
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Grant ID |
博甲第693号
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Grant Date |
2018-06-27
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Degree Name |
博士(医学)
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Grantor |
香川大学
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Set |
香川大学
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