DIFFERENT DNA CHANGES IN PRIMARY AND RECURRENT HEPATOCELLULAR-CARCINOMA

被引:10
作者
DING, SF
JALLEH, RP
WOOD, CB
BOWLES, L
DELHANTY, JDA
DOOLEY, J
HABIB, NA
机构
[1] HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT SURG,DU CANE RD,LONDON W12 0NN,ENGLAND
[2] UNIV LONDON UNIV COLL,DEPT GENET & BIOMETRY,LONDON WC1E 6BT,ENGLAND
[3] UNIV LONDON,DEPT SURG,LONDON,ENGLAND
[4] ROYAL FREE HOSP,SCH MED,DEPT MED,LONDON,ENGLAND
[5] HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT SURG,LONDON W12 0HS,ENGLAND
关键词
D O I
10.1136/gut.33.10.1433
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
DNA restriction fragment length polymorphism analysis was carried out on a primary and recurrent hepatocellular carcinoma in a hepatitis B virus negative patient. For the primary tumour, allele losses were found on the short arm of chromosome 17 (probe: p144-D6, 17p13) and the long arm of chromosome 5 with the probe Lambda MS8 (5q35-qter); other probes showed either no allele loss or a non-informative pattern. The recurrent cancer also showed allele loss with p144-D6, but not with Lambda MS8. In addition, the recurrent tumour had allele losses with Lambda MS43 (12q24.3-qter), pYNZ22 (17p13), and DNA rearrangement revealed by the probe Lambda MS32 (1q42-43), a pattern not seen in the primary lesion. These results indicate that the second hepatocellular carcinoma was of independent clonality and probably represents a de novo neoplasm rather than a recurrence.
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页码:1433 / 1435
页数:3
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