Large variation in t(11;14)(q13;q32) and t(14;18)(q32;q21) translocation product size is confirmed by sequence analysis of PCR products

Summary Polymerase chain reaction is commonly used to detect t(11;14)(q13;q32) and t(14;18)(q32;q21) chromosomal translocations associated with mantle cell lymphoma and follicular lymphoma. We tested a total of 482 samples from patients with suspected non‐Hodgkin's lymphoma and sequenced unusua...

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Veröffentlicht in:Clinical and laboratory haematology 2006-08, Vol.28 (4), p.248-253
Hauptverfasser: WICKHAM, C. L., HARRIES, L. W., SARSFIELD, P., JOYNER, M. V., ELLARD, S.
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Sprache:eng
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Zusammenfassung:Summary Polymerase chain reaction is commonly used to detect t(11;14)(q13;q32) and t(14;18)(q32;q21) chromosomal translocations associated with mantle cell lymphoma and follicular lymphoma. We tested a total of 482 samples from patients with suspected non‐Hodgkin's lymphoma and sequenced unusual‐sized t(11;14)(q13;q32) and t(14;18)(q32;q21) products from 33 of these patients. BCL‐1 or BCL‐2 gene rearrangements were confirmed in 23 of 33 patients (70%). Considerable size variation was observed using t(11;14) primers, with MTCA and MTCB t(11;14) products ranging from 234 to 934 bp and 143 to 560 bp respectively. Less variability was observed for t(14;18) Major Breakpoint Region (MBR) products (100–252 bp) but Minor Cluster Region (MCR) products ranged from 217 to 498 bp. We demonstrate the utility of sequence analysis to confirm unusual‐sized translocation products and reduce false‐positive results because of nonspecific amplification.
ISSN:0141-9854
1365-2257
DOI:10.1111/j.1365-2257.2006.00790.x