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Clinical Chemistry 50: 1479-1480, 2004; 10.1373/clinchem.2004.034694
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(Clinical Chemistry. 2004;50:1479-1480.)
© 2004 American Association for Clinical Chemistry, Inc.


Letters to the Editor

Rapid Detection of UGT1A1 Gene Polymorphisms by Newly Developed Invader Assay

Yoshinori Hasegawa1,a, Takeshi Sarashina2, Maki Ando1, Chiyoe Kitagawa1, Atsuo Mori2, Masao Yoneyama2, Yuichi Ando3 and Kaoru Shimokata1

1 Department of Medicine, Division of Respiratory Diseases, Nagoya University, Graduate School of Medicine, Nagoya, Japan. 2 Genomic Business Planning Department, Daiichi Pure Chemicals Co., Tokyo, Japan. 3 Department of Clinical Oncology, Saitama Medical School, Saitama, Japan

aAddress correspondence to this author at: Department of Medicine, Division of Respiratory Diseases, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. Fax 81-52-744-2176; e-mail yhasega@med.nagoya-u.ac.jp.

The first 20% of the full text of this article appears below.


To the Editor:

Recent progress in human genome analysis has been providing tools for a new approach to disease treatment based on individual differences identified by use of genetic information. The feasibility of genotyping for DNA polymorphisms before treatment depends on the availability of rapid, accurate, and efficient genotyping methods. We previously reported that genetic polymorphisms of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene were significantly related to severe toxicity of irinotecan (1). We now report that we have succeeded in detecting a 2-bp insertion of repeated sequence in the UGT1A1 gene by use of Invader assay technology.

Sixty patients who had received irinotecan-containing chemotherapy from July 1994 to June 1999 were enrolled in this study. All gave informed consent in writing for their peripheral blood to be used for the research. We used the QIAamp Blood Kit (QIAGEN GmbH) to prepare genomic DNA from whole blood (100–200 µL) and genotyped three sites of DNA polymorphisms in UGT1A1 (UGT1A1*28, UGT1A1*6, and UGT1A1*27) by the previously described method (1). UGT1A1*28 was distinguished . . . [Full Text of this Article]




The following articles in journals at HighWire Press have cited this article:


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J. Mol. Diagn.Home page
U. Ehmer, T. O. Lankisch, T. J. Erichsen, S. Kalthoff, N. Freiberg, M. Wehmeier, M. P. Manns, and C. P. Strassburg
Rapid Allelic Discrimination by TaqMan PCR for the Detection of the Gilbert's Syndrome Marker UGT1A1*28
J. Mol. Diagn., November 1, 2008; 10(6): 549 - 552.
[Abstract] [Full Text] [PDF]


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JNCI J Natl Cancer InstHome page
J. M. Hoskins, R. M. Goldberg, P. Qu, J. G. Ibrahim, and H. L. McLeod
UGT1A1*28 Genotype and Irinotecan-Induced Neutropenia: Dose Matters
J Natl Cancer Inst, September 5, 2007; 99(17): 1290 - 1295.
[Abstract] [Full Text] [PDF]




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