Article Text

PDF
MGMT methylation in diffuse large B-cell lymphoma: validation of quantitative methylation-specific PCR and comparison with MGMT protein expression
  1. S Uccella1,
  2. R Cerutti1,
  3. C Placidi1,
  4. S Marchet1,
  5. I Carnevali1,
  6. B Bernasconi1,
  7. I Proserpio2,
  8. G Pinotti2,
  9. M G Tibiletti3,
  10. D Furlan1,
  11. C Capella1
  1. 1
    Dept of Human Morphology, Unit of Pathology, University of Insubria–Ospedale di Circolo, Varese, Italy
  2. 2
    Dept of Oncology, Ospedale di Circolo, Varese, Italy
  3. 3
    Dept of Pathology, Ospedale di Circolo, Varese, Italy
  1. Dr S Uccella, Dept of Human Morphology, Unit of Pathology, University of Insubria, Via O. Rossi, 9, 21100 Varese, Italy; silvia.uccella{at}uninsubria.it

Abstract

Aims: (1) To validate a quantitative real time methylation specific PCR assay (MethyLight) for the detection of O6-methylguanine-DNA methyltransferase (MGMT) gene methylation status (MS) in diffuse large B-cell lymphoma (DLBCL). (2) To determine the immunohistochemical (IHC) expression of the MGMT protein and correlate it with MS. Both IHC and MethyLight results were compared with patient’s outcome.

Methods: 71 patients with primary nodal DLBCL were studied. MGMT immunoreactivity was detected using a specific monoclonal antibody. The MS of MGMT gene was analysed in 52/71 DLBCL using MethyLight. A selected subset of 40 DLBCL was also analysed using qualitative methylation-specific PCR (MSP). Statistical analysis of overall survival (OS), lymphoma-specific survival (LSS) and progression free survival (PFS) was performed according to IHC and MS results.

Results: 19/71 DLBCLs (27%) were MGMT-negative at IHC; all were analysed, together with 33/52 MGMT-positive DLBCLs. MethyLight showed a better performance than MSP. There was a good correlation between the presence of MGMT expression and the unmethylated status; the absence of IHC expression was poorly correlated with the presence of methylation. Better OS, LSS and PFS was found in DLBCLs with MGMT gene methylation. DLBCLs not expressing MGMT at IHC showed a longer PFS.

Conclusions: The quantitative real-time methylation-specific PCR assay for the detection of MGMT gene hypermethylation has been validated for the first time in DLBCL. Immunohistochemistry seems to represent an useful preliminary test to identify unmethylated cases; MS analysis may be performed in non-immunoreactive cases to identify truly methylated DLBCLs, which bear a better prognosis.

Statistics from Altmetric.com

Footnotes

  • Competing interests: None.

  • Contributions: SU conceived the study, collected, analysed, and interpreted the data and wrote the paper. RC performed the molecular study, interpreted the results and gave final approval. CP performed the immunohistochemical study, interpreted the results and gave final approval. SM performed the immunohistochemical study, interpreted the results and gave final approval. IC performed the molecular study and gave final approval. BB performed the cytogenetic study and gave final approval. IP collected clinical data and gave final approval. GP collected and interpreted clinical data and gave final approval. MGT collected and interpreted cytogenetic data and gave final approval. DF collected, analysed and interpreted molecular data, wrote part of the paper and gave final approval. CC conceived the study, analysed and interpreted the data, revised the manuscript and gave final approval.

  • Ethics approval: Ethics approval was obtained.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.