INI1 immunohistochemical expression in glioblastoma: correlation with MGMT gene promoter methylation status and patient survival

被引:8
|
作者
Zunarelli, Elena [1 ]
Bigiani, Nazzarena [1 ]
Sartori, Giuliana [1 ]
Migaldi, Mario [1 ]
Sgambato, Alessandro [2 ]
Maiorana, Antonio [1 ]
机构
[1] Azienda Osped Univ Policlin, Sect Pathol Anat, I-41124 Modena, Italy
[2] Univ Cattolica Sacro Cuore, Ist Patol Gen, Ctr Ric Oncol Giovanni XXIII, Rome, Italy
关键词
Glioblastoma; immunohistochemistry; INI1 (HSNF5/BAF47/SMARCB1); MGMT; survival; ATYPICAL TERATOID/RHABDOID TUMORS; PRIMITIVE NEUROECTODERMAL TUMORS; NEWLY-DIAGNOSED GLIOBLASTOMA; MALIGNANT RHABDOID TUMORS; CENTRAL-NERVOUS-SYSTEM; SOFT-TISSUE; ADJUVANT TEMOZOLOMIDE; EPITHELIOID SARCOMA; PHASE-III; RADIOTHERAPY;
D O I
10.1097/PAT.0b013e328340bb26
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims: INI1 expression and its correlation with MGMT gene promoter methylation status and follow-up was investigated in 77 surgically removed glioblastomas then treated with radiotherapy (RT) or AT plus temozolomide (RT+TMZ). Methods: INI1 was determined by immunohistochemistry and MGMT by methylation-specific PCR. Results: INI1 was expressed in 83.1% of cases. The median overall survival (OS) was 13.6 months in INI1 positive tumours and 7.2 months in INI1 negative tumours; 31.3% of patients with INI1 positive tumours were alive compared with 15.4% of patients with INI1 negative tumours. MGMT methylation was detected in 31.2% of cases. OS was significantly different between patients with methylated tumours and unmethylated tumours (p<0.04), and between patients with RT+TMZ and AT alone (p<0.001). Considering both treatment and MGMT, the difference in OS was significant (p<0.002). The difference in OS according to MGMT and INI1 was significant (p<0.04). The longest median OS was recorded among methylated and INI1 positive tumours. Among unmethylated tumours, the median OS was 11.1 months in INI1 positive and 6.5 months in INI1 negative tumours. No patients were alive with unmethylated and INI1 negative tumours. Conclusions: Loss of INI1 immunohistochemical expression in glioblastoma may be indicating an underlying molecular aberration accounting for the more aggressive clinical behaviour.
引用
收藏
页码:17 / 23
页数:7
相关论文
共 50 条
  • [41] The different role of YKL-40 in glioblastoma is a function of MGMT promoter methylation status
    Chen, Wei-jun
    Zhang, Xiang
    Han, Hua
    Lv, Jian-nan
    Kang, En-ming
    Zhang, Yu-lian
    Liu, Wei-ping
    He, Xiao-sheng
    Wang, James
    Wang, Gui-huai
    Yu, Yan-bing
    Zhang, Wei
    CELL DEATH & DISEASE, 2020, 11 (08)
  • [42] Prognostic Role of Methylation Status of the MGMT Promoter Determined Quantitatively by Pyrosequencing in Glioblastoma Patients
    Kim, Dae Cheol
    Kim, Ki Uk
    Kim, Young Zoon
    JOURNAL OF KOREAN NEUROSURGICAL SOCIETY, 2016, 59 (01) : 26 - 36
  • [43] Weak MGMT gene promoter methylation confers a clinically significant survival benefit in patients with newly diagnosed glioblastoma: a retrospective cohort study
    Pinson, H.
    Hallaert, G.
    Van der Meulen, J.
    Dedeurwaerdere, F.
    Vanhauwaert, D.
    Van den Broecke, C.
    Van Dorpe, J.
    Van Roost, D.
    Kalala, J. P.
    Boterberg, T.
    JOURNAL OF NEURO-ONCOLOGY, 2020, 146 (01) : 55 - 62
  • [44] Heterogeneity of MGMT gene promoter methylation and protein expression in serial specimens in newly diagnosed glioblastoma
    Pan, Qiang
    Yang, Xue-Jun
    Zhu, Lin
    Song, Chun-Yu
    Diao, Xing-Tao
    Gao, Yong
    Zhu, Jun
    Yue, Xiao
    Li, Hu-Guang
    Cheng, Wei-Ling
    Ning, Yi-Ping
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2016, 9 (09): : 17356 - 17366
  • [45] Improved risk stratification in younger IDH wild-type glioblastoma patients by combining a 4-miRNA signature with MGMT promoter methylation status
    Unger, Kristian
    Fleischmann, Daniel F.
    Ruf, Viktoria
    Felsberg, Joerg
    Piehlmaier, Daniel
    Samaga, Daniel
    Hess, Julia
    Suresh, Marian Preetham
    Mittelbronn, Michel
    Lauber, Kirsten
    Budach, Wilfried
    Sabel, Michael
    Roedel, Claus
    Reifenberger, Guido
    Herms, Jochen
    Tonn, Joerg-Christian
    Zitzelsberger, Horst
    Belka, Claus
    Niyazi, Maximilian
    NEURO-ONCOLOGY ADVANCES, 2020, 2 (01)
  • [46] The TERT promoter mutation status and MGMT promoter methylation status, combined with dichotomized MRI-derived and clinical features, predict adult primary glioblastoma survival
    Shu, Chang
    Wang, Qiong
    Yan, Xiaoling
    Wang, Jinhuan
    CANCER MEDICINE, 2018, 7 (08): : 3704 - 3712
  • [47] Association of MGMT Gene Promoter Methylation With Clinicopathological Parameters in Patients With Wild-type IDH Glioblastoma
    Kim, Moonsik
    Yoo, Jihwan
    Chang, Jong Hee
    Kim, Se Hoon
    ANTICANCER RESEARCH, 2022, 42 (01) : 335 - 341
  • [48] Methylation status of the MGMT gene promoter fails to predict the clinical outcome of glioblastoma patients treated with ACNU plus cisplatin
    Park, Chul-Kee
    Park, Sung-Hye
    Lee, Se-Hoon
    Kim, Chae-Yong
    Kim, Dong-Wan
    Paek, Sun Ha
    Kim, Dong Gyu
    Heo, Dae Seog
    Kim, Il Han
    Jung, Hee-Won
    NEUROPATHOLOGY, 2009, 29 (04) : 443 - 449
  • [49] Defining the cutoff value of MGMT gene promoter methylation and its predictive capacity in glioblastoma
    Brigliadori, Giovanni
    Foca, Flavia
    Dall'Agata, Monia
    Rengucci, Claudia
    Melegari, Elisabetta
    Cerasoli, Serenella
    Amadori, Dino
    Calistri, Daniele
    Faedi, Marina
    JOURNAL OF NEURO-ONCOLOGY, 2016, 128 (02) : 333 - 339
  • [50] Identification of regions correlating MGMT promoter methylation and gene expression in glioblastomas
    Everhard, Sibille
    Tost, Joerg
    El Abdalaoui, Hafida
    Criniere, Emmanuelle
    Busato, Florence
    Marie, Yannick
    Gut, Ivo G.
    Sanson, Marc
    Mokhtari, Karima
    Laigle-Donadey, Florence
    Hoang-Xuan, Khe
    Delattre, Jean-Yves
    Thillet, Joelle
    NEURO-ONCOLOGY, 2009, 11 (04) : 348 - 356