EARLY DIAGNOSIS OF MYELODYSPLASTIC SYNDROMES USING CLONAL ANALYSES

• Published in: Chinese journal of cancer research Vol. 14; no. 3; pp. 225 - 229
• Main Authors: Qian, Jun, Xue, Yong-quan, Yu, Fei, Wu, Ya-fang, Pan, Jin-lan, Lu, Ding-wei
• Format: Journal Article
• Language: English
• Published: Jiangsu Institute of Hematology, Leukemia Research Unit, First Affiliated Hospital, Soochow University, Suzhou 215006 01.09.2002
• Subjects: analysis; chromatid; Clonal; Cytogenetics; diagnosis; differentiation; Early; Fluorescence; hybridization; mutation; Myelodysplastic; N-ras; Sister; situ; syndrome; Early diagnosis; Fluorescence in situ hybridization; N-ras mutation; Cytogenetics; Sister chromatid differentiation; Clonal analysis; Myelodysplastic syndrome
• ISSN: 1000-9604; 1993-0631
• DOI: 10.1007/s11670-002-0050-3

Objective: To study the value of clonal analysis to the early diagnosis of myelodysplastic syndrome (MDS). Methods: Four types of clonal analyses were performed on the bone marrow samples from 50 patients suspected of MDS: (1) Conventional Cytogenetics (CC) for clonal chromosomal abnormalities; (2) BrdU-Sister Chromatid Differentiation (BrdU-SCD) for cell cycle kinetics; (3) Fluorescence in Situ Hybridization (FISH) for trisomy 8; (4) Polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) for N-ras mutation. Results: The diagnosis of forty-three patients was compatible with the FAB criteria for MDS. The other seven cases didn't meet the FAB criteria, with only one lineage of dyspoiesis or with no obvious dysplastic changes. Among these seven cases, two were morphologically diagnosed with suspicious refractory anemia, one with sideroblastic anemia, one with leukemoid reaction, one with hypercellular anemia and two with chronic aplastic anemia. Clonal analyses of the 7 patients showed that six cases had clonal karyotype abnormalities, four had prolonged cell cycle patterns, four had trisomy 8 of different proportions and one had mutation of the exon 1 of N-RAS. Thus, they were revaluated as MDS patients. Conclusion: The untypical MDS patients with one lineage dyspoiesis or without obvious dysplastic changes can be diagnosed early by combining multiple clonal analysis techniques such as CC, SCD, FISH and PCR-SSCR.