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Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia

Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia
Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia
Promoter methylation is a common phenomenon in tumours, including haematological malignancies. In the present study, we investigated 36 cases of high hyperdiploid (>50 chromosomes) acute lymphoblastic leukaemia (ALL) with methylation-specific multiplex ligase-dependent probe amplification to determine the extent of aberrant methylation in this subgroup. The analysis, which comprised the promoters of 35 known tumour suppressor genes, showed that 16 genes displayed abnormal methylation in at least one case each. The highest number of methylated gene promoters seen in a single case was thirteen, with all but one case displaying methylation for at least one gene. The most common targets were ESR1 (29/36 cases; 81%), CADM1 (IGSF4, TSLC1; 25/36 cases; 69%), FHIT (24/36 cases; 67%) and RARB (22/36 cases; 61%). Interestingly, quantitative reverse transcription-polymerase chain reaction showed that although methylation of the CADM1 and RARB promoters resulted in the expected pattern of downregulation of the respective genes, no difference could be detected in FHIT expression between methylation-positive and -negative cases. Furthermore, TIMP3 was not expressed regardless of methylation status, showing that aberrant methylation does not always lead to gene expression changes. Taken together, our findings suggest that aberrant methylation of tumour suppressor gene promoters is a common phenomenon in high hyperdiploid ALL
high hyperdiploid, methylation, acute lymphoblastic leukaemia
0007-1048
838-847
Paulsson, Kajsa
19187fef-73b1-4808-b7ec-c1468849b61b
An, Qian
6766de29-63b7-45eb-b21a-04cac9921373
Moorman, Anthony V.
e4ced178-ee03-47ef-bc5e-25d8453951d5
Parker, Helen
33e0cd81-d45f-49bc-9539-09345d79d895
Molloy, Gael
3881bfbd-407b-479f-9cfe-824753e89d8c
Davies, Teresa
7feaa1c8-4ab7-4ac9-b350-136c8bc4af34
Griffiths, Mike
f147af96-79ab-43ef-984c-550407b82c39
Ross, Fiona M.
ec0958f8-b992-4e4a-b7e3-c474600390ba
Irving, Julie
d6d4ae90-4a64-45f6-8c2a-360cf71cb999
Harrison, Christine J.
52da7673-509c-4b88-b92e-0c021c9c7d3e
Young, Bryan D.
d6d3ff53-6b73-42e7-8d41-19d1f16c58d2
Strefford, Jon C.
3782b392-f080-42bf-bdca-8aa5d6ca532f
Paulsson, Kajsa
19187fef-73b1-4808-b7ec-c1468849b61b
An, Qian
6766de29-63b7-45eb-b21a-04cac9921373
Moorman, Anthony V.
e4ced178-ee03-47ef-bc5e-25d8453951d5
Parker, Helen
33e0cd81-d45f-49bc-9539-09345d79d895
Molloy, Gael
3881bfbd-407b-479f-9cfe-824753e89d8c
Davies, Teresa
7feaa1c8-4ab7-4ac9-b350-136c8bc4af34
Griffiths, Mike
f147af96-79ab-43ef-984c-550407b82c39
Ross, Fiona M.
ec0958f8-b992-4e4a-b7e3-c474600390ba
Irving, Julie
d6d4ae90-4a64-45f6-8c2a-360cf71cb999
Harrison, Christine J.
52da7673-509c-4b88-b92e-0c021c9c7d3e
Young, Bryan D.
d6d3ff53-6b73-42e7-8d41-19d1f16c58d2
Strefford, Jon C.
3782b392-f080-42bf-bdca-8aa5d6ca532f

Paulsson, Kajsa, An, Qian, Moorman, Anthony V., Parker, Helen, Molloy, Gael, Davies, Teresa, Griffiths, Mike, Ross, Fiona M., Irving, Julie, Harrison, Christine J., Young, Bryan D. and Strefford, Jon C. (2009) Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia. British Journal of Haematology, 144 (6), 838-847. (doi:10.1111/j.1365-2141.2008.07523.x). (Submitted)

Record type: Article

Abstract

Promoter methylation is a common phenomenon in tumours, including haematological malignancies. In the present study, we investigated 36 cases of high hyperdiploid (>50 chromosomes) acute lymphoblastic leukaemia (ALL) with methylation-specific multiplex ligase-dependent probe amplification to determine the extent of aberrant methylation in this subgroup. The analysis, which comprised the promoters of 35 known tumour suppressor genes, showed that 16 genes displayed abnormal methylation in at least one case each. The highest number of methylated gene promoters seen in a single case was thirteen, with all but one case displaying methylation for at least one gene. The most common targets were ESR1 (29/36 cases; 81%), CADM1 (IGSF4, TSLC1; 25/36 cases; 69%), FHIT (24/36 cases; 67%) and RARB (22/36 cases; 61%). Interestingly, quantitative reverse transcription-polymerase chain reaction showed that although methylation of the CADM1 and RARB promoters resulted in the expected pattern of downregulation of the respective genes, no difference could be detected in FHIT expression between methylation-positive and -negative cases. Furthermore, TIMP3 was not expressed regardless of methylation status, showing that aberrant methylation does not always lead to gene expression changes. Taken together, our findings suggest that aberrant methylation of tumour suppressor gene promoters is a common phenomenon in high hyperdiploid ALL

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More information

Submitted date: March 2009
Keywords: high hyperdiploid, methylation, acute lymphoblastic leukaemia

Identifiers

Local EPrints ID: 69944
URI: http://eprints.soton.ac.uk/id/eprint/69944
ISSN: 0007-1048
PURE UUID: 7fe6ea52-983f-4b53-9ffe-6088e6519bcb
ORCID for Helen Parker: ORCID iD orcid.org/0000-0001-8308-9781
ORCID for Jon C. Strefford: ORCID iD orcid.org/0000-0002-0972-2881

Catalogue record

Date deposited: 11 Dec 2009
Last modified: 14 Mar 2024 02:49

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Contributors

Author: Kajsa Paulsson
Author: Qian An
Author: Anthony V. Moorman
Author: Helen Parker ORCID iD
Author: Gael Molloy
Author: Teresa Davies
Author: Mike Griffiths
Author: Fiona M. Ross
Author: Julie Irving
Author: Christine J. Harrison
Author: Bryan D. Young

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