Preliminary individual adjuvant chemotherapy for primary central nervous system lymphomas based on the expression of drug-resistance genes

被引:10
作者
Kunishio K. [1 ,2 ]
Okada M. [1 ]
Matsumoto Y. [1 ]
Nagao S. [1 ]
机构
[1] Department of Neurological Surgery, Kagawa University, Kito-gun, Kagawa 761-0793
[2] Department of Neurosurgery, Kawasaki Hospital, Okayama, Okayama 700-8505
关键词
Central nervous system lymphoma; Chemotherapy; Drug-resistance gene;
D O I
10.1007/BF02484511
中图分类号
学科分类号
摘要
Individual adjuvant chemotherapy based on the expression of drug-resistance genes by reverse transcription-polymerase chain reaction (RT-PCR) was applied for the treatment of patients with primary central nervous system lymphoma (PCNSL). Three patients were included in this study. The drug-resistance genes were investigated in tumor tissues by RT-PCR with the specific primers for MDR-1, MRP-1, MRP-2, MXR-1, MGMT, GST-pei, and topoisomerase II alpha. We selected proper anticancer agents based on mRNA expression of these drug-resistance genes. In case 1, RT-PCR showed overexpression of MDR-1, MRP-1, MGMT, and topoisomerase II alpha mRNA, whereas neither MRP-2, MXR-1, nor GST-pei was expressed. The patient was given high-dose methotrexate (HD-MTX) for the first cycle of treatment; however, the reduced tumor showed regrowth before the second cycle of treatment, and therefore the patient was given carboplatin, mitoxantrone, and HD-MTX in the second and third cycles. Finally, magnetic resonance (MR) images showed a complete response. The other two cases showed similar patterns of drug-resistance gene expression, such that mRNAs of MRP-2, MXR-1, MGMT, GST-pei, and topoisomerase II alpha were overexpressed, whereas neither MDR-1 nor MRP-1 was expressed. They were successfully treated with combined HD-MTX and CHOP (cyclophosphamide, doxorubicin, vincristine, and predonsone). Our preliminary trial of individual adjuvant chemotherapy based on RT-PCR suggested that it was an effective and beneficial therapy for PCNSL. Although HD-MTX therapy is supposed to be effective for patients with MDR-1-negative PCNSL, MTX alone should be avoided in the choice of the anticancer drug for the treatment of MDR-1-positive PCNSL.
引用
收藏
页码:57 / 61
页数:4
相关论文
共 34 条
[1]
Becker I., Becker K.F., Meyermann R., Et al., The multidrug-resistance gene MDR1 is expressed in human glial tumours, Acta Neuropathol, 82, pp. 516-519, (1991)
[2]
Kirches E., Oda Y., Von Bossanyi P., Et al., Mdr1 mRNA expression differs between grade III astrocytomas and glioblastomas, Clin Neuropathol, 16, pp. 34-36, (1997)
[3]
Lee J.S., Scala S., Matsumoto Y., Et al., Reduced drug accumulation and multidrug resistance in human breast cancer cells without associated P-glycoprotein or MRP overexpression, J Cell Biochem, 65, pp. 513-526, (1997)
[4]
Nabors M.W., Griffin C.A., Zehnbauer B.A., Et al., Multidrug resistance gene (MDR1) expression in human brain tumors, J Neurosurg, 75, pp. 941-946, (1991)
[5]
Cole S.P.C., Bhardwaj G., Gerlach J.H., Et al., Overexpression of a transporter gene in a multidrug-resistance human lung cancer cell line, Science, 258, pp. 1650-1654, (1992)
[6]
Fojo A.T., Ueda K., Slamon D.J., Et al., Expression of multidrug-resistance gene in human tumors and tissues, Proc Natl Acad Sci USA, 84, pp. 265-269, (1987)
[7]
Grant C.E., Vadimarsson G., Hipfner D.R., Et al., Overexpression of multidrug resistance-associated protein (MRP) increases resistance to natural product drugs, Cancer Res, 54, pp. 357-361, (1994)
[8]
Kool M., De Mass M., Scheffer G.L., Et al., Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines, Cancer Res, 57, pp. 3537-3547, (1997)
[9]
Matsumoto Y., Takano H., Fojo T., Cellular adaptation to drug exposure: Evolution of the drug-resistance phenotype, Cancer Res, 57, pp. 5086-5092, (1997)
[10]
Mineura K., Yanagisawa T., Watanabe K., Et al., Human brain tumor O<sup>6</sup>-methylguanine-DNA methyltransferase mRNA and its significance as an indicator of selective chloroethylnitrosourea chemotherapy, Int J Cancer, 69, pp. 420-425, (1996)