2011•Chinese Clinical OncologyRequires access

MGMT gene promoter methylation in malignant melanoma patients

Ju Guo

Open publisher page 0 citations

Abstract

Objective This study was designed to investigate the association of MGMT promoter methylation and MGMT protein expression in Chinese malignant melanoma patients.Methods We analyzed the MGMT promoter methylation by methylation-specific polymerase chain reaction(MS-PCR) and protein expression by immunohistochemistry(IHC) in 44 malignant melanoma cases.Results We found that MGMT promoter hypermethylation occurred in 18 of 44(40.9%) cases,MGMT protein expression rate of MGMT promoter methylation patients was 27.8%(5/18) and MGMT protein expression rate of MGMT promoter unmethylation patients was 65.4%(17/26).The presence of hypermethylation was associated with loss of MGMT protein(P=0.014).Conclusion In the advanced malignant melanoma MGMT promoter methylation may reduce MGMT protein expression;the examination of MGMT promoter methylation status in melanoma may be useful for stratefying patients with melanoma into suitable chemotherapy such as alkylating agents,and offer theoretical and practical basis to personalized treatments.

About this research paper

What this paper is about

Objective This study was designed to investigate the association of MGMT promoter methylation and MGMT protein expression in Chinese malignant melanoma patients.Methods We analyzed the MGMT promoter methylation by methylation-specific polymerase chain reaction(MS-PCR) and protein expression by immunohistochemistry(IHC) in 44 malignant melanoma cases.Results We found that MGMT promoter hypermethylation occurred in 18 of 44(40.9%) cases,MGMT protein expression rate of MGMT promoter methylation patients was 27.8%(5/18) and MGMT protein expression rate of MGMT promoter unmethylation patients was 65.4%(17/26).The presence of hypermethylation was associated with loss of MGMT protein(P=0.014).Conclusion In the advanced malignant melanoma MGMT promoter methylation may reduce MGMT protein expression;the examination of MGMT promoter methylation status in melanoma may be useful for stratefying patients with melanoma into suitable chemotherapy such as alkylating agents,and offer theoretical and practical basis to personalized treatments.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective This study was designed to investigate the association of MGMT promoter methylation and MGMT protein expression in Chinese malignant melanoma patients.Methods We analyzed the MGMT promoter methylation by methylation-specific polymerase chain reaction(MS-PCR) and protein expression by immunohistochemistry(IHC) in 44 malignant melanoma cases.Results We found that MGMT promoter hypermethylation occurred in 18 of 44(40.9%) cases,MGMT protein expression rate of MGMT promoter methylation patients was 27.8%(5/18) and MGMT protein expression rate of MGMT promoter unmethylation patients was 65.4%(17/26).The presence of hypermethylation was associated with loss of MGMT protein(P=0.014).Conclusion In the advanced malignant melanoma MGMT promoter methylation may reduce MGMT protein expression;the examination of MGMT promoter methylation status in melanoma may be useful for stratefying patients with melanoma into suitable chemotherapy such as alkylating agents,and offer theoretical and practical basis to personalized treatments.

Key concepts: Methylation, Cancer research, Melanoma, Medicine, Immunohistochemistry, DNA methylation, Promoter, Gene

Related papers

Back to paper searchBrowse research topicsOriginal source
MGMT gene promoter methylation in malignant melanoma patients — Research Paper | ScholarLens