Multidrug Resistence and Breast Cancer

作者: Gengyin Zhou , Xiaofang Zhang

DOI: 10.5772/24414

关键词:

摘要: Millions of new cancer patients are diagnosed each year and over half these die from this disease. As the second leading cause deaths, breast is estimated to be in one million people worldwide more than 400,000 deaths [1]. Chemotherapy part a successful treatment many cases; however, development multidrug resistance (MDR) it becomes major obstacle so as few treated benefit chemotherapy. MDR term used describe phenomenon characterized by ability drug resistant tumors exhibit simultaneous number structurally functionally unrelated chemotherapeutic agents [2]. The cytotoxic drugs that most frequently associated with hydrophobic, amphipathic natural products, such taxanes (paclitaxel docetaxel), vinca alkaloids (vinorelbine, vincristine, vinblastine), anthracyclines (doxorubicin, daunorubicin, epirubicin), epipodophyllotoxins (etoposide teniposide), antimetabolites (methorexate, fluorouracil, cytosar, 5-azacytosine, 6-mercaptopurine, gemcitabine) topotecan, dactinomycin, mitomycin C on[3]. At present, mechanisms have been found responsible for it, including overexpression members adenosine triphosphate (ATP)-binding cassette (ABC) membrane transporter family, changes apoptosis-related genes, alteration DNArepair gene, stem cells on. And up date, methods were adopted overcome MDR, example natrual drugs, chemical genetic therapy. Herein, we will introduce therapy briefly.

参考文章(141)
Alfred H Schinkel, John D Allen, Multidrug resistance and pharmacological protection mediated by the breast cancer resistance protein (BCRP/ABCG2) Molecular Cancer Therapeutics. ,vol. 1, pp. 427- 434 ,(2002)
Tero Jarvinen, Edison Liu, HER-2/neu and topoisomerase IIalpha--simultaneous drug targets in cancer. Combinatorial Chemistry & High Throughput Screening. ,vol. 6, pp. 455- 470 ,(2003) , 10.2174/138620703106298635
A. Shukla, G. S. Shukla, N. S. Radin, Control of kidney size by sex hormones: possible involvement of glucosylceramide. American Journal of Physiology-renal Physiology. ,vol. 262, ,(1992) , 10.1152/AJPRENAL.1992.262.1.F24
Bert L. Lum, Michael P. Gosland, MDR expression in normal tissues. Pharmacologic implications for the clinical use of P-glycoprotein inhibitors. Hematology-oncology Clinics of North America. ,vol. 9, pp. 319- 336 ,(1995) , 10.1016/S0889-8588(18)30097-2
Douglas D. Ross, Judith E. Karp, Tar T. Chen, L. Austin Doyle, Expression of breast cancer resistance protein in blast cells from patients with acute leukemia Blood. ,vol. 96, pp. 365- 368 ,(2000) , 10.1182/BLOOD.V96.1.365.013K46_365_368
Spence Rk, Emerging trends in surgical blood transfusion. Seminars in Hematology. ,vol. 34, pp. 48- 53 ,(1997)
E. Teodori, S. Dei, S. Scapecchi, F. Gualtieri, The medicinal chemistry of multidrug resistance (MDR) reversing drugs. Farmaco. ,vol. 57, pp. 385- 415 ,(2002) , 10.1016/S0014-827X(02)01229-6
L. V. Abruzzo, D. D. Ross, T. Krogmann, A. K. Rishi, L. A. Doyle, Y. Gao, Wei Tse Yang, Erratum: A multidrug resistance transporter from human MCF-7 breast cancer cells (Proceedings of the National Academy of Sciences of the USA (December 22, 1998) 95 (15665-15670)) Proceedings of the National Academy of Sciences of the United States of America. ,vol. 96, ,(1999)
Fengxi Su, Xiaoqu Hu, Weijuan Jia, Chang Gong, Erwei Song, Peter Hamar, Glutathion s transferase π indicates chemotherapy resistance in breast cancer Journal of Surgical Research. ,vol. 113, pp. 102- 108 ,(2003) , 10.1016/S0022-4804(03)00200-2
F. P. O'Malley, S. Chia, D. Tu, L. E. Shepherd, M. N. Levine, V. H. Bramwell, I. L. Andrulis, K. I. Pritchard, Topoisomerase II Alpha and Responsiveness of Breast Cancer to Adjuvant Chemotherapy Journal of the National Cancer Institute. ,vol. 101, pp. 644- 650 ,(2009) , 10.1093/JNCI/DJP067