TY - JOUR
T1 - MS-MLPA
T2 - An attractive alternative laboratory assay for robust, reliable, and semiquantitative detection of MGMT promoter hypermethylation in gliomas
AU - Jeuken, Judith W.M.
AU - Cornelissen, Sandra J.B.
AU - Vriezen, Martine
AU - Dekkers, Marieke M.G.
AU - Errami, Abdellatif
AU - Sijben, Angelique
AU - Boots-Sprenger, Sandra H.E.
AU - Wesseling, Pieter
N1 - Funding Information:
This project was sponsored by the Dutch Cancer Society (Koningin Wilhelmina Fonds: KUN 2004-3143) and the Pauline van Everdingen Foundation. We thank Jan Schouten from MRC-Holland for developing and kindly supplying the MGMT MS-MLPA kits and for helpful discussions. We also thank Dr Hans Bernsen (CWZ), Dr Mathé Prick (CWZ) and Dr Anja Gijtenbeek (RUNMC) for providing the clinical information, and the neurosurgeons of the RUNMC and CWZ for their continuous collaboration.
PY - 2007/10
Y1 - 2007/10
N2 - Expression of the DNA repair protein O6-alkylguanine-DNA-alkyltransferase (AGT), encoded by the O6-methylguanine (O6-mG) -DNA-methyltransferase (MGMT) DNA repair gene, results in resistance to alkylating agents, and hypermethylation of the MGMT promoter is associated with chemosensitivity as it prevents AGT expression. As the interpretation of the results of immunohistochemistry to evaluate AGT expression proved to be difficult, the aim of our present study is to establish a feasible, reliable, and robust method for MGMT promoter hypermethylation testing that can be easily implemented in a diagnostic setting and is applicable to routinely processed tissue. MGMT hypermethylation analysis using methylation-specific (MS-) multiplex ligation-dependent probe amplification (MLPA) was performed on 62 glioma samples of 55 individual tumors (including 12 cell lines) and compared to the more conventionally used, but improved, MS-polymerase chain reaction (PCR). In contrast to MS-PCR, MS-MLPA (i) is not based on bisulfite conversion of unmethylated cytosines (a somewhat troublesome step in MS-PCR), (ii) provided methylation status of all samples, (iii) proved to be semiquantitative, (iv) can be used to evaluate methylation status of multiple sequences (CpG dinucleotides) simultaneously, and (v) allows for a combined copy number detection and methylation specific analysis. The potential therapeutic value of MGMT hypermethylation evaluation using MS-MLPA was shown in a group of 20 glioblastoma patients receiving temozolomide chemotherapy. We conclude that MS-MLPA is a robust and reliable method that can be easily applied to differently processed tissues, including those fixed in formalin and embedded in paraffin. The semiquantitative aspect of MS-MLPA may prove to be of great value, especially in predicting response to alkylating agents, not only for gliomas as evaluated in this study but also for tumors in general.
AB - Expression of the DNA repair protein O6-alkylguanine-DNA-alkyltransferase (AGT), encoded by the O6-methylguanine (O6-mG) -DNA-methyltransferase (MGMT) DNA repair gene, results in resistance to alkylating agents, and hypermethylation of the MGMT promoter is associated with chemosensitivity as it prevents AGT expression. As the interpretation of the results of immunohistochemistry to evaluate AGT expression proved to be difficult, the aim of our present study is to establish a feasible, reliable, and robust method for MGMT promoter hypermethylation testing that can be easily implemented in a diagnostic setting and is applicable to routinely processed tissue. MGMT hypermethylation analysis using methylation-specific (MS-) multiplex ligation-dependent probe amplification (MLPA) was performed on 62 glioma samples of 55 individual tumors (including 12 cell lines) and compared to the more conventionally used, but improved, MS-polymerase chain reaction (PCR). In contrast to MS-PCR, MS-MLPA (i) is not based on bisulfite conversion of unmethylated cytosines (a somewhat troublesome step in MS-PCR), (ii) provided methylation status of all samples, (iii) proved to be semiquantitative, (iv) can be used to evaluate methylation status of multiple sequences (CpG dinucleotides) simultaneously, and (v) allows for a combined copy number detection and methylation specific analysis. The potential therapeutic value of MGMT hypermethylation evaluation using MS-MLPA was shown in a group of 20 glioblastoma patients receiving temozolomide chemotherapy. We conclude that MS-MLPA is a robust and reliable method that can be easily applied to differently processed tissues, including those fixed in formalin and embedded in paraffin. The semiquantitative aspect of MS-MLPA may prove to be of great value, especially in predicting response to alkylating agents, not only for gliomas as evaluated in this study but also for tumors in general.
KW - Diagnostic marker
KW - Glioma
KW - Methylation specific MLPA
KW - Methylation specific PCR
KW - MGMT
KW - Promoter hypermethylation
KW - Tailor-made therapy
UR - http://www.scopus.com/inward/record.url?scp=34548760880&partnerID=8YFLogxK
U2 - 10.1038/labinvest.3700664
DO - 10.1038/labinvest.3700664
M3 - Article
C2 - 17700563
AN - SCOPUS:34548760880
SN - 0023-6837
VL - 87
SP - 1055
EP - 1065
JO - Laboratory Investigation
JF - Laboratory Investigation
IS - 10
ER -