Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice
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Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice
Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice
中国结合医学杂志(英文版)2016年22卷第10期 页码:752-758
Affiliations:
1. School of Basic Medical Science, Shandong University of Traditional Chinese Medicine,Jinan,China
2. Department of Neurology, Qilu Hospital, Shandong University,Jinan,China
3. Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine,Shanghai,China
Author bio:
Funds:
Supported by the National Natural Science Foundation of China (No. 81072832, 81273634), and the Opening Project of Shanghai Key Laboratory of Complex Prescription (No. 11DZ2272300), National Science and Technology Major Projects for "Major New Drugs Innovation and Development (No. 2010Z0940)
Ji, Xm., Wu, Zc., Liu, Gw. et al. Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice., Chin. J. Integr. Med. 22, 752–758 (2016). https://doi.org/10.1007/s11655-015-2087-4
Xu-ming Ji, Zhi-chun Wu, Guo-wei Liu, et al. Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice[J]. Chinese Journal of Integrative Medicine, 2016,22(10):752-758.
Ji, Xm., Wu, Zc., Liu, Gw. et al. Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice., Chin. J. Integr. Med. 22, 752–758 (2016). https://doi.org/10.1007/s11655-015-2087-4DOI:
Xu-ming Ji, Zhi-chun Wu, Guo-wei Liu, et al. Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice[J]. Chinese Journal of Integrative Medicine, 2016,22(10):752-758. DOI: 10.1007/s11655-015-2087-4.
Wenxia Changfu Formula (温下肠腑方) induces apoptosis of lung adenocarcinoma in a transplanted tumor model of drug-resistance nude mice
摘要
To explore the apoptosis mechanism of Wenxia Changfu Formula (温下肠腑方
WCF) in reversing drug resistance of lung cancer in vivo. Thirty model mice were randomly assigned to three groups: control group
cisplatin (CDDP) group
and WCF group. A transplanted tumor model of lung adenocarcinoma was established in all groups. Mice in the WCF group received intragastric administration of WCF (0.2 mL/10 g body weight) everyday in addition to CDDP intraperitoneally (5 mg/kg body weight) twice a week. The mice in the CDDP group received CDDP intraperitoneally (5 mg/kg body weight) twice a week
while the control group received normal saline intraperitoneally (0.2 mL/10 g body weight) everyday. The weight of the nude mice and respective tumors
tumor volume and tumor-inhibiting rate were measured. Electron microscopy was used to observe the existence of apoptosis body. Apoptosis index (AI) was detected by TdT-mediated dUTP nick end labeling staining. The expression of Fas and FasL mRNA was investigated by reverse transcription polymerase chain reaction
while immunohistochemistry was applied to detect the protein expression of Fas and FasL
caspase-3 and caspase-activated DNase (CAD)
respectively. Compared with CDDP group and control group
WCF could significantly reduce the tumor volume from the 19th day and alleviate the tumor weight (P <0.05)
and the apoptosis body was found in tumor cells in the WCF group. WCF could also enhance the level of AI
up-regulate the expression of caspase apoptosis pathway related protein caspase-3 and CAD
as well as the expression of Fas
FasL mRNA and protein (P <0.05). WCF could improve the sensitivity of tumor cells to CDDP and reverse the drug resistance by inducing the apoptosis.
Abstract
To explore the apoptosis mechanism of Wenxia Changfu Formula (温下肠腑方
WCF) in reversing drug resistance of lung cancer in vivo. Thirty model mice were randomly assigned to three groups: control group
cisplatin (CDDP) group
and WCF group. A transplanted tumor model of lung adenocarcinoma was established in all groups. Mice in the WCF group received intragastric administration of WCF (0.2 mL/10 g body weight) everyday in addition to CDDP intraperitoneally (5 mg/kg body weight) twice a week. The mice in the CDDP group received CDDP intraperitoneally (5 mg/kg body weight) twice a week
while the control group received normal saline intraperitoneally (0.2 mL/10 g body weight) everyday. The weight of the nude mice and respective tumors
tumor volume and tumor-inhibiting rate were measured. Electron microscopy was used to observe the existence of apoptosis body. Apoptosis index (AI) was detected by TdT-mediated dUTP nick end labeling staining. The expression of Fas and FasL mRNA was investigated by reverse transcription polymerase chain reaction
while immunohistochemistry was applied to detect the protein expression of Fas and FasL
caspase-3 and caspase-activated DNase (CAD)
respectively. Compared with CDDP group and control group
WCF could significantly reduce the tumor volume from the 19th day and alleviate the tumor weight (P <0.05)
and the apoptosis body was found in tumor cells in the WCF group. WCF could also enhance the level of AI
up-regulate the expression of caspase apoptosis pathway related protein caspase-3 and CAD
as well as the expression of Fas
FasL mRNA and protein (P <0.05). WCF could improve the sensitivity of tumor cells to CDDP and reverse the drug resistance by inducing the apoptosis.
关键词
Wenxia Changfu Formulaanimal modeldrug resistanceapoptosisin vivo
Keywords
Wenxia Changfu Formulaanimal modeldrug resistanceapoptosisin vivo
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Department of Biochemistry, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran
Department of Immunology, School of Medical Sciences, Tarbiat Modares University, Tehran
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Department of Nursing, Min-Hwei College of Health Care Management, Tainan
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