Diagnostic Significance and Clinical Applications of Chimeric Genes in Ewing's Sarcoma
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- Yoshino Naoko
- Clinical Pharmacy, College of Pharmacy, Nihon University
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- Kojima Tetsuko
- Clinical Pharmacy, College of Pharmacy, Nihon University
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- Asami Satoru
- Clinical Pharmacy, College of Pharmacy, Nihon University
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- Motohashi Shigeyasu
- Clinical Pharmacy, College of Pharmacy, Nihon University
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- Yoshida Yoshikazu
- Department of Hospital Pharmacy, School of Medicine, Nihon University
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- Chin Motoaki
- Department of Advanced Medicine, Division of Cell Regeneration and Transplantation, School of Medicine, Nihon University
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- Shichino Hiroyuki
- Department of Advanced Medicine, Division of Cell Regeneration and Transplantation, School of Medicine, Nihon University
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- Yoshida Yukihiro
- Department of Orthopedics, School of Medicine, Nihon University
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- Nemoto Norimichi
- Department of Pathology, School of Medicine, Nihon University
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- Kaneko Michio
- Department of Pediatric Surgery, Institute of Clinical Medicine, University of Tsukuba
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- Mugishima Hideo
- Department of Advanced Medicine, Division of Cell Regeneration and Transplantation, School of Medicine, Nihon University
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- Suzuki Takashi
- Clinical Pharmacy, College of Pharmacy, Nihon University
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説明
Ewing's sarcoma (ES) is one of the most malignant bone and soft tissue tumors in childhood. Morphologically, ES belongs to the small round cell tumors (SRCT). ES, peripheral primitive neuroectodermal tumor (PNET), and Askin's tumor are classified as ES family tumors (ESFT) because they share a common chromosomal translocation. The EWS-FLI1 chimeric gene is generated by t (11; 22). Other reciprocal translocations resulting in formation of chimeric genes between EWS and ETS family genes (ERG, ETV1, E1AF, and FEV) are t (21; 22), t (7; 22), t (17; 22), and t (2; 22), respectively. Although it is generally difficult to distinguish ES from SRCT, we could easily and quickly distinguish ES from other SRCT by using reverse transcription polymerase chain reaction (RT-PCR). We looked for specific chimeric genes in 23 tumor samples, including three ES clinical samples. We detected five chimeric genes in the three ES samples. Three chimeric genes, all EWS-FLI1, were detected in one ES sample. Different chimeric genes, EWS-ERG and EWS-ETV1, were detected in the other two ES samples. Moreover, because we could not detect specific chimeric genes in samples from non-ESFT, it may be possible to use this technique to diagnose ESFT and to detect tumor cell contamination before hematopoietic stem cell transplantation.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 26 (5), 585-588, 2003
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204625634560
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- NII論文ID
- 110003608479
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- NII書誌ID
- AA10885497
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- COI
- 1:CAS:528:DC%2BD3sXltVejurg%3D
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 6516998
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- PubMed
- 12736494
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可