Role of MGMT as biomarker in colorectal cancer

被引:31
|
作者
Inno, Alessandro [1 ]
Fanetti, Giuseppe [2 ]
Di Bartolomeo, Maria [3 ]
Gori, Stefania [1 ]
Maggi, Claudia [3 ]
Cirillo, Massimo [1 ]
Iacovelli, Roberto [3 ]
Nichetti, Federico [3 ]
Martinetti, Antonia [3 ]
de Braud, Filippo [3 ]
Bossi, Ilaria [3 ]
Pietrantonio, Filippo [3 ]
机构
[1] Osped Sacro Cuore Don Calabria, Med Oncol Dept, I-37100 Verona, Italy
[2] European Inst Oncol, Radiotherapy Unit, I-20100 Milan, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Med Oncol Dept, Via Venezian, I-20100 Milan, Italy
关键词
Colorectal cancer; O6-methylguanine DNA methyltransferase; Temozolomide; Dacarbazine; Biomarker;
D O I
10.12998/wjcc.v2.i12.835
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
O-6-methylguanine DNA methyltransferase (MGMT) gene promoter methylation plays an important role in colorectal carcinogenesis, occurring in about 30%-40% of metastatic colorectal cancer. Its prognostic role has not been defined yet, but loss of expression of MGMT, which is secondary to gene promoter methylation, results in an interesting high response to alkylating agents such as dacarbazine and temozolomide. In a phase 2 study on heavily pre-treated patients with MGMT methylated metastatic colorectal cancer, temozolomide achieved about 30% of disease control rate. Activating mutations of RAS or BRAF genes as well as mismatch repair deficiency may represent mechanisms of resistance to alkylating agents, but a dose-dense schedule of temozolomide may potentially restore sensitivity in RAS -mutant patients. Further development of temozolomide in MGMT methylated colorectal cancer includes investigation of synergic combinations with other agents such as fluoropyrimidines and research for additional biomarkers, in order to better define the role of temozolomide in the treatment of individual patients. (c) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:835 / 839
页数:5
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