Quantitative digital assessment of MGMT immunohistochemical expression in glioblastoma tissue

被引:20
作者
Araki, Yukie [1 ]
Mizoguchi, Masahiro [1 ]
Yoshimoto, Koji [1 ]
Shono, Tadahisa [1 ]
Amano, Toshiyuki [1 ]
Nakamizo, Akira [1 ]
Suzuki, Satoshi O. [2 ]
Iwaki, Toru [2 ]
Sasaki, Tomio [1 ]
机构
[1] Kyushu Univ, Dept Neurosurg, Grad Sch Med Sci, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Dept Neuropathol, Grad Sch Med Sci, Fukuoka 8128582, Japan
关键词
O-6-methylguanine methyltransferase (MGMT); Glioblastoma; Immunohistochemistry; Quantitative assessment; O-6-METHYLGUANINE-DNA METHYLTRANSFERASE; PROMOTER HYPERMETHYLATION; PROGNOSTIC-SIGNIFICANCE; O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE; ADJUVANT TEMOZOLOMIDE; MOLECULAR MARKERS; METHYLATION; SURVIVAL; GLIOMA; GENE;
D O I
10.1007/s10014-010-0004-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent reports have suggested an important clinical role for hypermethylation of the O-6-methylguanine-DNA-methyltransferase (MGMT) promoter in patients with glioblastomas. Whether MGMT protein expression is correlated with promoter hypermethylation and patient outcomes, however, has not been elucidated. Here we describe a quantitative digital method for assessment of MGMT-specific immunostaining, and analyze the relationship between expression levels and methylation status of the MGMT promoter. We investigated 46 tumors from patients who received a diagnosis of glioblastoma or gliosarcoma. Immunohistochemistry with anti-MGMT antibody and methylation-specific PCR using bisulfite-modified tumor DNA were performed. The digital assessment method used image-analysis software to determine a digital MGMT staining index, and the results were compared with those obtained via conventional visual assessments. The digital staining index clearly correlated with the methylation status of MGMT promoter. In addition, the index correlated with our observational results when nuclear and cytoplasmic staining were assessed in three different fields. Our digital assessment method enabled us to assess uncertain immunopositive samples objectively and quantitatively, which is an important consideration when examining heterogeneous cellular staining. We expect that this method will be useful for assessment of heterogeneous staining with any antibodies.
引用
收藏
页码:25 / 31
页数:7
相关论文
共 32 条
[1]   Relationship between expression of O6-methylguanine-DNA methyltransferase, glutathione-S-transferase, π in glioblastoma and the survival of the patients treated with nimustine hydrochloride:: An immunohistochemical analysis [J].
Anda, T ;
Shabani, HK ;
Tsunoda, K ;
Tokunaga, Y ;
Kaminogo, M ;
Shibata, S ;
Hayashi, T ;
Iseki, M .
NEUROLOGICAL RESEARCH, 2003, 25 (03) :241-248
[2]   Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomas [J].
Brell, M ;
Tortosa, A ;
Verger, E ;
Gil, JM ;
Viñolas, N ;
Villá, S ;
Acebes, JJ ;
Caral, L ;
Pujol, T ;
Ferrer, I ;
Ribalta, T ;
Graus, F .
CLINICAL CANCER RESEARCH, 2005, 11 (14) :5167-5174
[3]   A simplified laboratory validated assay for MGMT promoter hypermethylation analysis of glioma specimens from formalin-fixed paraffin-embedded tissue [J].
Cankovic, Milena ;
Mikkelsen, Tom ;
Rosenblum, Mark L. ;
Zarbo, Richard J. .
LABORATORY INVESTIGATION, 2007, 87 (04) :392-397
[4]   THE CORRELATION AND PROGNOSTIC SIGNIFICANCE OF MGMT PROMOTER METHYLATION AND MGMT PROTEIN IN GLIOBLASTOMAS [J].
Cao, Van Thang ;
Lung, Tae-Young ;
Jung, Shin ;
Jin, Shu-Guang ;
Moon, Kyung-Sub ;
Kim, In-Young ;
Kang, Sam-Suk ;
Park, Chang-Soo ;
Lee, Kyung-Hwa ;
Chae, Hong-Jae .
NEUROSURGERY, 2009, 65 (05) :866-875
[5]   Antitumor activity of rapamycin in a phase I trial for patients with recurrent PTEN-Deficient glioblastoma [J].
Cloughesy, Tim F. ;
Yoshimoto, Koji ;
Nghiemphu, Phioanh ;
Brown, Kevin ;
Dang, Julie ;
Zhu, Shaojun ;
Hsueh, Teli ;
Chen, Yinan ;
Wang, Wei ;
Youngkin, David ;
Liau, Linda ;
Martin, Neil ;
Becker, Don ;
Bergsneider, Marvin ;
Lai, Albert ;
Green, Richard ;
Oglesby, Tom ;
Koleto, Michael ;
Trent, Jeff ;
Horvath, Steve ;
Mischel, Paul S. ;
Mellinghoff, Ingo K. ;
Sawyers, Charles L. .
PLOS MEDICINE, 2008, 5 (01) :139-151
[6]   Molecular markers of gliomas: a clinical approach [J].
Eoli, M. ;
Silvani, A. ;
Pollo, B. ;
Bianchessi, D. ;
Menghi, F. ;
Valletta, L. ;
Broggi, G. ;
Boiardi, A. ;
Bruzzone, M. G. ;
Finocchiaro, G. .
NEUROLOGICAL RESEARCH, 2006, 28 (05) :538-541
[7]   Inactivation of the DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents [J].
Esteller, M ;
Garcia-Foncillas, J ;
Andion, E ;
Goodman, SN ;
Hidalgo, OF ;
Vanaclocha, V ;
Baylin, SB ;
Herman, JG .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (19) :1350-1354
[8]   Prognostic Significance of Molecular Markers and Extent of Resection in Primary Glioblastoma Patients [J].
Felsberg, Joerg ;
Rapp, Marion ;
Loeser, Simon ;
Fimmers, Rolf ;
Stummer, Walter ;
Goeppert, Matthias ;
Steiger, Hans-Jacob ;
Friedensdorf, Britta ;
Reifenberger, Guido ;
Sabel, Michael C. .
CLINICAL CANCER RESEARCH, 2009, 15 (21) :6683-6693
[9]   Clinical relevance of MGMT in the treatment of cancer [J].
Gerson, SL .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (09) :2388-2399
[10]   Intratumoral homogeneity of MGMT promoter hypermethylation as demonstrated in serial stereotactic specimens from anaplastic astrocytomas and glioblastomas [J].
Grasbon-Frodl, Eva M. ;
Kreth, Friedrich Wilhelm ;
Ruiter, Michael ;
Schnell, Oliver ;
Bise, Karl ;
Felsberg, Joerg ;
Reifenberger, Guido ;
Tonn, Joerg-Christian ;
Kretzschmar, Hans A. .
INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (11) :2458-2464