Zhong, Xh., Wang, Lb. & Sun, Dz. Effects of inotodiol extracts from inonotus obliquus on proliferation cycle and apoptotic gene of human lung adenocarcinoma cell line A549., Chin. J. Integr. Med. 17, 218–223 (2011). https://doi.org/10.1007/s11655-011-0670-x
Xiu-hong Zhong, Li-bo Wang, Dong-zhi Sun. Effects of inotodiol extracts from inonotus obliquus on proliferation cycle and apoptotic gene of human lung adenocarcinoma cell line A549[J]. Chinese Journal of Integrative Medicine, 2011,17(3):218-223.
Zhong, Xh., Wang, Lb. & Sun, Dz. Effects of inotodiol extracts from inonotus obliquus on proliferation cycle and apoptotic gene of human lung adenocarcinoma cell line A549., Chin. J. Integr. Med. 17, 218–223 (2011). https://doi.org/10.1007/s11655-011-0670-xDOI:
Xiu-hong Zhong, Li-bo Wang, Dong-zhi Sun. Effects of inotodiol extracts from inonotus obliquus on proliferation cycle and apoptotic gene of human lung adenocarcinoma cell line A549[J]. Chinese Journal of Integrative Medicine, 2011,17(3):218-223. DOI: 10.1007/s11655-011-0670-x.
Effects of inotodiol extracts from inonotus obliquus on proliferation cycle and apoptotic gene of human lung adenocarcinoma cell line A549
摘要
To observe the proliferation inhibition
apoptosis
and cell proliferation cycle of human lung carcinoma cell line A549 treated with Inotodiol extracts from Inonotus obliquus and explore the possibility of Inotodiol extracts from Inonotus obliquus as a new tumor chemopreventive drug. Human lung cancer cell line A549 was treated with different concentrations of Inotodiol
the effects of Inotodiol on cell apoptosis
the expression of Ki-67
Bcl-2
Bax
and p53 and cell cycle were detected by TUNEL assay
immunohistochemistry
and flow cytometry assay respectively. Inotodiol extracts had antiproliferation effect on human lung carcinoma cell line A549. The expression of Ki-67 decreased with the increase of Inotodiol concentration and exposure time (P<0.05)
in a dose-dependent and time-dependent manner. The typical characteristics of the apoptosis of A549 cells treated with Inotodiol were observed
and the apoptotic rate of A549 cell at 48 h was the highest by TUNEL assay. Inotodiol arrested A549 cells in the S phase
and apoptotic peak was observed by flow cytometry. Immunocytochemistry indicated that the expression of Bcl-2 protein decreased
while the expression of p53 and Bax proteins increased in A549 cells treated with Inotodiol
compared with the control cells (P<0.05). Inotodiol can inhibit proliferation and induce the apoptosis of A549 cells
and its molecular mechanism may be associated with the up-regulating expression of p53 and bax proteins and down-regulating expression of Bcl-2 protein
which arrested A549 cells in S phase.
Abstract
To observe the proliferation inhibition
apoptosis
and cell proliferation cycle of human lung carcinoma cell line A549 treated with Inotodiol extracts from Inonotus obliquus and explore the possibility of Inotodiol extracts from Inonotus obliquus as a new tumor chemopreventive drug. Human lung cancer cell line A549 was treated with different concentrations of Inotodiol
the effects of Inotodiol on cell apoptosis
the expression of Ki-67
Bcl-2
Bax
and p53 and cell cycle were detected by TUNEL assay
immunohistochemistry
and flow cytometry assay respectively. Inotodiol extracts had antiproliferation effect on human lung carcinoma cell line A549. The expression of Ki-67 decreased with the increase of Inotodiol concentration and exposure time (P<0.05)
in a dose-dependent and time-dependent manner. The typical characteristics of the apoptosis of A549 cells treated with Inotodiol were observed
and the apoptotic rate of A549 cell at 48 h was the highest by TUNEL assay. Inotodiol arrested A549 cells in the S phase
and apoptotic peak was observed by flow cytometry. Immunocytochemistry indicated that the expression of Bcl-2 protein decreased
while the expression of p53 and Bax proteins increased in A549 cells treated with Inotodiol
compared with the control cells (P<0.05). Inotodiol can inhibit proliferation and induce the apoptosis of A549 cells
and its molecular mechanism may be associated with the up-regulating expression of p53 and bax proteins and down-regulating expression of Bcl-2 protein
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相关机构
Department of Integrated Traditional Chinese and Western Medicine, Second Affiliated Hospital of Medical School of Xi’an Jiaotong University
School of Public Health of Xi’an Jiaotong University
Department of Nephrology, Second Affiliated Hospital of Medical School of Xi’an Jiaotong University
Department of Pharmacy, Harbin Commercial University
Department of Endocrine, People’s Hospital Affiliated to Fujian University of Traditional Chinese Medicine