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Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts

Many traditional Chinese medicine (TCM) formulae have been used in cancer therapy. The JIN formula is an ancient herbal formula recorded in the classic TCM book Jin Kui Yao Lue (Golden Chamber). The JIN formula significantly delayed the growth of subcutaneous human H460 xenografted tumors in vivo co...

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Detalles Bibliográficos
Autores principales: Zheng, Luyu, Zhang, Weiyi, Jiang, Miao, Zhang, Huarong, Xiong, Fei, Yu, Yang, Chen, Meijuan, Zhou, Jing, Dai, Xiaoming, Tang, Yuping, Jiang, Ming, Wang, Mingyan, Cheng, Ge, Duan, Jinao, Yu, Wei, Lin, Biaoyang, Fu, Haian, Zhang, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770002/
https://www.ncbi.nlm.nih.gov/pubmed/24066008
http://dx.doi.org/10.1155/2013/160168
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author Zheng, Luyu
Zhang, Weiyi
Jiang, Miao
Zhang, Huarong
Xiong, Fei
Yu, Yang
Chen, Meijuan
Zhou, Jing
Dai, Xiaoming
Tang, Yuping
Jiang, Ming
Wang, Mingyan
Cheng, Ge
Duan, Jinao
Yu, Wei
Lin, Biaoyang
Fu, Haian
Zhang, Xu
author_facet Zheng, Luyu
Zhang, Weiyi
Jiang, Miao
Zhang, Huarong
Xiong, Fei
Yu, Yang
Chen, Meijuan
Zhou, Jing
Dai, Xiaoming
Tang, Yuping
Jiang, Ming
Wang, Mingyan
Cheng, Ge
Duan, Jinao
Yu, Wei
Lin, Biaoyang
Fu, Haian
Zhang, Xu
author_sort Zheng, Luyu
collection PubMed
description Many traditional Chinese medicine (TCM) formulae have been used in cancer therapy. The JIN formula is an ancient herbal formula recorded in the classic TCM book Jin Kui Yao Lue (Golden Chamber). The JIN formula significantly delayed the growth of subcutaneous human H460 xenografted tumors in vivo compared with the growth of mock controls. Gene array analysis of signal transduction in cancer showed that the JIN formula acted on multiple targets such as the mitogen-activated protein kinase, hedgehog, and Wnt signaling pathways. The coformula treatment of JIN and diamminedichloroplatinum (DDP) affected the stress/heat shock pathway. Proteomic analysis showed 36 and 84 differentially expressed proteins between the mock and DDP groups and between the mock and JIN groups, respectively. GoMiner analysis revealed that the differentially expressed proteins between the JIN and mock groups were enriched during cellular metabolic processes, and so forth. The ones between the DDP and mock groups were enriched during protein-DNA complex assembly, and so forth. Most downregulated proteins in the JIN group were heat shock proteins (HSPs) such as HSP90AA1 and HSPA1B, which could be used as markers to monitor responses to the JIN formula therapy. The mechanism of action of the JIN formula on HSP proteins warrants further investigation.
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spelling pubmed-37700022013-09-24 Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts Zheng, Luyu Zhang, Weiyi Jiang, Miao Zhang, Huarong Xiong, Fei Yu, Yang Chen, Meijuan Zhou, Jing Dai, Xiaoming Tang, Yuping Jiang, Ming Wang, Mingyan Cheng, Ge Duan, Jinao Yu, Wei Lin, Biaoyang Fu, Haian Zhang, Xu Evid Based Complement Alternat Med Research Article Many traditional Chinese medicine (TCM) formulae have been used in cancer therapy. The JIN formula is an ancient herbal formula recorded in the classic TCM book Jin Kui Yao Lue (Golden Chamber). The JIN formula significantly delayed the growth of subcutaneous human H460 xenografted tumors in vivo compared with the growth of mock controls. Gene array analysis of signal transduction in cancer showed that the JIN formula acted on multiple targets such as the mitogen-activated protein kinase, hedgehog, and Wnt signaling pathways. The coformula treatment of JIN and diamminedichloroplatinum (DDP) affected the stress/heat shock pathway. Proteomic analysis showed 36 and 84 differentially expressed proteins between the mock and DDP groups and between the mock and JIN groups, respectively. GoMiner analysis revealed that the differentially expressed proteins between the JIN and mock groups were enriched during cellular metabolic processes, and so forth. The ones between the DDP and mock groups were enriched during protein-DNA complex assembly, and so forth. Most downregulated proteins in the JIN group were heat shock proteins (HSPs) such as HSP90AA1 and HSPA1B, which could be used as markers to monitor responses to the JIN formula therapy. The mechanism of action of the JIN formula on HSP proteins warrants further investigation. Hindawi Publishing Corporation 2013 2013-08-20 /pmc/articles/PMC3770002/ /pubmed/24066008 http://dx.doi.org/10.1155/2013/160168 Text en Copyright © 2013 Luyu Zheng et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zheng, Luyu
Zhang, Weiyi
Jiang, Miao
Zhang, Huarong
Xiong, Fei
Yu, Yang
Chen, Meijuan
Zhou, Jing
Dai, Xiaoming
Tang, Yuping
Jiang, Ming
Wang, Mingyan
Cheng, Ge
Duan, Jinao
Yu, Wei
Lin, Biaoyang
Fu, Haian
Zhang, Xu
Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts
title Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts
title_full Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts
title_fullStr Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts
title_full_unstemmed Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts
title_short Expression Profiling and Proteomic Analysis of JIN Chinese Herbal Formula in Lung Carcinoma H460 Xenografts
title_sort expression profiling and proteomic analysis of jin chinese herbal formula in lung carcinoma h460 xenografts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770002/
https://www.ncbi.nlm.nih.gov/pubmed/24066008
http://dx.doi.org/10.1155/2013/160168
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