Please use this identifier to cite or link to this item: https://doi.org/10.1097/FPC.0b013e32831ebb5d
Title: Chemotherapy-induced tumor gene expression changes in human breast cancers
Authors: Lee, S.-C. 
Xu, X.
Lim, Y.-W.
Lau, P.
Sukri, N.
Lim, S.-E.
Yap, H.L.
Yeo, W.-L.
Tan, P.
Tan, S.-H.
McLeod, H.
Goh, B.-C.
Keywords: Breast cancer
Chemotherapy
Docetaxel
Doxorubicin
Drug resistance
Gene expression
Issue Date: Mar-2009
Citation: Lee, S.-C., Xu, X., Lim, Y.-W., Lau, P., Sukri, N., Lim, S.-E., Yap, H.L., Yeo, W.-L., Tan, P., Tan, S.-H., McLeod, H., Goh, B.-C. (2009-03). Chemotherapy-induced tumor gene expression changes in human breast cancers. Pharmacogenetics and Genomics 19 (3) : 181-192. ScholarBank@NUS Repository. https://doi.org/10.1097/FPC.0b013e32831ebb5d
Abstract: Objective Studying chemotherapy-induced gene expression changes in vivo, which could provide insights into mechanisms of chemotherapy resistance. Methods We analyzed and compared tumor gene expression changes of about 38500 genes before and 3 weeks after doxorubicin or docetaxel treatment in 47 breast cancer patients. Results By using the median expression level of each probe set as the parameter, less than 5% of genes were upregulated or downregulated by more than 50% after treatment with either drug. Doxorubicin and docetaxel concordantly induced 251 genes predominantly involved in protein and macromolecule metabolism (upregulated), and cell cycle and DNA/RNA metabolism (downregulated). Doxorubicin treatment resulted in coregulation of a cluster of 345 probe sets involved in focal adhesion, Jak-Stat signaling pathway, cell adhesion molecules, and natural killer cell mediated cytotoxicity, whereas docetaxel treatment resulted in coregulation of a cluster of 448 probe sets involved in focal adhesion, neurodegenerative disorders, sphingolipid metabolism, and cell cycle. Tumors that were intrinsically sensitive or resistant to doxorubicin or docetaxel evoked distinct gene expression changes in response to the drug; doxorubicin-resistant tumors upregulated genes that were enriched for ErbB signaling, ubiquitin-mediated proteolysis, TGF-β signaling, and MAP-kinase signaling pathways, whereas docetaxel-resistant tumors upregulated genes that were enriched for focal adhesion and regulation of actin cytoskeleton. The drug-specific tumor gene expression changes were validated in independent in-vitro and in-vivo datasets. Conclusion Gene expression alterations of breast cancer were specific to doxorubicin and docetaxel treatment, and yielded mechanistic insights into resistance to either drug. Gene expression analysis provides more global perspectives on resistance pathways that could be exploited for therapeutic selection. © 2009 Wolters Kluwer Health| Lippincott Williams & Wilkins.
Source Title: Pharmacogenetics and Genomics
URI: http://scholarbank.nus.edu.sg/handle/10635/116255
ISSN: 17446872
DOI: 10.1097/FPC.0b013e32831ebb5d
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