目的 介紹吉西他濱代謝酶對胰腺癌化療耐藥影響的研究進(jìn)展。
方法 復(fù)習(xí)和總結(jié)了近年來的相關(guān)文獻(xiàn),對吉西他濱代謝酶與胰腺癌化療耐藥關(guān)系的研究進(jìn)展加以綜述。
結(jié)果 hENT1、dCK、RRM1、CDA等代謝酶與胰腺癌對吉西他濱化療的耐藥具有密切關(guān)系; 代謝酶的單核苷酸多態(tài)性與胰腺癌對吉西他濱耐藥的關(guān)系仍有待研究。
結(jié)論 胰腺癌對吉西他濱化療耐藥是多因素、多因子共同作用的結(jié)果,對于代謝酶影響胰腺癌化療耐藥的機(jī)理有待進(jìn)一步研究。
引用本文: 袁田,廖泉,趙玉沛. 吉西他濱代謝酶與胰腺癌化療耐藥關(guān)系的研究進(jìn)展. 中國普外基礎(chǔ)與臨床雜志, 2009, 16(8): 613-616. doi: 復(fù)制
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13. | Spratlin J, Sangha R, Darry Glubrecht D, et al. The absence of human equilibrative nucleoside transporter 1 is associated with reduced survival in patients with gemcitabine-treated pancreas adenocarcinoma [J]. Clin Cancer Res, 2004; 10(20): 6956-6961. |
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27. | Sugiyama E, Kaniwa N, Kim SR, et al. Pharmacokinetics of gemcitabine in Japanese cancer patients: the impact of a cytidine deaminase polymorphism [J]. J Clin Oncol, 2007; 25(1): 32-42. |
28. | Nakano Y, Tanno S, Koizumi K, et al. Gemcitabine chemoresistance and molecular markers associated with gemcitabine transport and metabolism in human pancreatic cancer cells [J]. Br J Cancer, 2007; 96(3): 457-463. |
29. | 張立陽, 趙玉沛, 吳元德, 等. 胰腺癌阿霉素耐藥細(xì)胞株SW1990/ADM的建立及其耐藥機(jī)理研究 [J]. 中國普外基礎(chǔ)與臨床雜志, 2005; 12(1): 46-50. |
30. | 潘博, 郭俊超, 廖泉, 等. 吉西他濱與胰腺癌化療耐藥 [J]. 中國普外基礎(chǔ)與臨床雜志, 2005; 12(5): 530-532. |
- 1. Alexakis N, Halloran C, Raraty M, et al. Current standards of surgery for pancreatic cancer [J]. Br J Surg, 2004; 91(11): 1410-1427.
- 2. Abbruzzese JL. New applications of gemcitabine and future directions in the management of pancreatic cancer [J]. Cancer, 2002; 95 (4 Suppl): 941-945.
- 3. Burris HA 3rd, Moore MJ, Andersen J, et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial [J]. J Clin Oncol, 1997; 15(6): 2403-2413.
- 4. Mini E, Nobili S, Caciagli B, et al. Cellular pharmacology of gemcitabine [J]. Ann Oncol, 2006; 17 (Suppl 5): v7-v12.
- 5. Galmarini CM, Mackey JR, Dumontet C. Nucleoside analogues: mechanisms of drug resistance and reversal strategies [J]. Leukemia, 2001; 15(6): 875-890.
- 6. Shi JY, Shi ZZ, Zhang SJ, et al. Association between single nucleotide polymorphisms in deoxycytidine kinase and treatment response among acute myeloid leukaemia patients [J]. Pharmacogenetics, 2004; 14(11): 759-768.
- 7. Ward JL, Leung GP, Toan SV, et al. Functional analysis of site-directed glycosylation mutants of the human equilibrative nucleoside transporter-2 [J]. Arch Biochem Biophys, 2003; 411(1): 19-26.
- 8. García-Manteiga J, Molina-Arcas M, Casado FJ, et al. Nucleoside transporter profiles in human pancreatic cancer cells: role of hCNT1 in 2’, 2’-difluorodeoxycytidine-induced cytotoxicity [J]. Clin Cancer Res, 2003; 9(13): 5000-5008.
- 9. Mori R, Ishikawa T, Ichikawa Y, et al. Human equilibrative nucleoside transporter 1 is associated with the chemosensitivity of gemcitabine in human pancreatic adenocarcinoma and biliary tract carcinoma cells [J]. Oncol Rep, 2007; 17(5): 1201-1205.
- 10. Rauchwerger DR, Firby PS, Hedley DW, et al. Equilibrative-sensitive nucleoside transporter and its role in gemcitabine sensitivity [J]. Cancer Res, 2000; 60(21): 6075-6079.
- 11. Giovannetti E, Del Tacca M, Mey V, et al. Transcription analysis of human equilibrative nucleoside transporter-1 predicts survival in pancreas cancer patients treated with gemcitabine [J]. Cancer Res, 2006; 66(7): 3928-3935.
- 12. Farrell JJ, Elsaleh H, Garcia M, et al. Human equilibrative nucleoside transporter 1 levels predict response to gemcitabine in patients with pancreatic cancer [J]. Gastroenterology, 2009; 136(1): 187-195.
- 13. Spratlin J, Sangha R, Darry Glubrecht D, et al. The absence of human equilibrative nucleoside transporter 1 is associated with reduced survival in patients with gemcitabine-treated pancreas adenocarcinoma [J]. Clin Cancer Res, 2004; 10(20): 6956-6961.
- 14. Giovannetti E, Mey V, Nannizzi S, et al. Pharmacogenetics of anticancer drug sensitivity in pancreatic cancer [J]. Mol Cancer Ther, 2006; 5(6): 1387-1395.
- 15. Kroep JR, Loves WJ, van der Wilt CL, et al. Pretreatment deoxycytidine kinase levels predict in vivo gemcitabine sensitivity [J]. Mol Cancer Ther, 2002; 1(6): 371-376.
- 16. Blackstock AW, Lightfoot H, Case LD, et al. Tumor uptake and elimination of 2’, 2’-difluoro-2’-deoxycytidine (gemcitabine) after deoxycytidine kinase gene transfer: correlation with in vivo tumor response [J]. Clin Cancer Res, 2001; 7(10): 3263-3268.
- 17. Veuger MJ, Heemskerk MH, Honders MW, et al. Functional role of alternatively spliced deoxycytidine kinase in sensitivity to cytarabine of acute myeloid leukemic cells [J]. Blood, 2002; 99(4): 1373-1380.
- 18. Veuger MJ, Honders MW, Landegent JE, et al. High incidence of alternatively spliced forms of deoxycytidine kinase in patients with resistant acute myeloid leukemia [J]. Blood, 2000; 96(4): 1517-1524.
- 19. Galmarini CM, Clarke ML, Jordheim L, et al. Resistance to gemcitabine in a human follicular lymphoma cell line is due to partial deletion of the deoxycytidine kinase gene [J]. BMC Pharmacol, 2004; 4: 8-20.
- 20. Ohhashi S, Ohuchida K, Mizumoto K, et al. Down-regulation of deoxycytidine kinase enhances acquired resistance to gemcitabine in pancreatic cancer [J]. Anticancer Res, 2008; 28(4B): 2205-2212.
- 21. Szantai E, Ronai Z, Sasvari-Szekely M, et al. Multicapillary electrophoresis analysis of single-nucleotide sequence variations in the deoxycytidine kinase gene [J]. Clin Chem, 2006; 52(9): 1756-1762.
- 22. Sebastiani V, Ricci F, Rubio-Viqueira B, et al. Immunohistochemical and genetic evaluation of deoxycytidine kinase in pancreatic cancer: relationship to molecular mechanisms of gemcitabine resistance and survival [J]. Clin Cancer Res, 2006; 12(8): 2492-2497.
- 23. Davidson JD, Ma L, Flagella M, et al. An increase in the expression of ribonucleotide reductase large subunit 1 is associated with gemcitabine resistance in non-small cell lung cancer cell lines [J]. Cancer Res, 2004; 64(11): 3761-3766.
- 24. Bergman AM, Eijk PP, Ruiz van Haperen VW, et al. In vivo induction of resistance to gemcitabine resultsin increased expression of ribonucleotide reductase subunit M1 as the major determinant [J]. Cancer Res, 2005; 65(20): 9510-9516.
- 25. Guex N, Peitsch MC. SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling [J]. Electrophoresis, 1997; 18(15): 2714-2723.
- 26. Yonemori K, Ueno H, Okusaka T, et al. Severe drug toxicity associated with a single-nucleotide polymorphism of the cytidine deaminase gene in a Japanese cancer patient treated with gemcitabine plus cisplatin [J]. Clin Cancer Res, 2005; 11(7): 2620-2624.
- 27. Sugiyama E, Kaniwa N, Kim SR, et al. Pharmacokinetics of gemcitabine in Japanese cancer patients: the impact of a cytidine deaminase polymorphism [J]. J Clin Oncol, 2007; 25(1): 32-42.
- 28. Nakano Y, Tanno S, Koizumi K, et al. Gemcitabine chemoresistance and molecular markers associated with gemcitabine transport and metabolism in human pancreatic cancer cells [J]. Br J Cancer, 2007; 96(3): 457-463.
- 29. 張立陽, 趙玉沛, 吳元德, 等. 胰腺癌阿霉素耐藥細(xì)胞株SW1990/ADM的建立及其耐藥機(jī)理研究 [J]. 中國普外基礎(chǔ)與臨床雜志, 2005; 12(1): 46-50.
- 30. 潘博, 郭俊超, 廖泉, 等. 吉西他濱與胰腺癌化療耐藥 [J]. 中國普外基礎(chǔ)與臨床雜志, 2005; 12(5): 530-532.