The Role of Transforming Growth Factor Beta and Smad Receptors in Determining Prognosis in High-Grade Primary Brain Tumors: Glioblastoma Multiforme

被引:0
作者
Gursoy, Gueven [1 ]
Barutcuoglu, Mustafa [2 ]
Sivrikoz, Oya Nermin [3 ]
Gokalp, Sevtap [4 ]
Vatansever, Seda [5 ]
机构
[1] Mugla Training & Res Hosp, Dept Neurosurg, Mugla, Turkey
[2] Manisa Celal Bayar Univ, Fac Med, Dept Neurosurg, Manisa, Turkey
[3] Baskent Univ, Zubeyde Hanim Training & Res Hosp, Dept Pathol, Izmir, Turkey
[4] Maltepe Univ, Dept Histol & Embryol, Istanbul, Turkey
[5] Manisa Celal Bayar Univ, Fac Med, Dept Histol & Embryol, Manisa, Turkey
来源
BRAZILIAN NEUROSURGERY-ARQUIVOS BRASILEIROS DE NEUROCIRURGIA | 2023年 / 42卷 / 02期
关键词
glioblastoma multiforme; transforming growth factor beta; smad proteins; endothelial-mesenchymal transition; S-PHASE FRACTION; TGF-BETA; CANCER; KI-67;
D O I
10.1055/s-0042-1743555
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction High-grade primary brain tumors cause serious morbidity and mortality. This study aimed to investigate the role of transforming growth factor beta (TGF-beta) and suppressor of mothers against decapentaplegic (Smad) receptors in high-grade primary brain tumors. \Material and Method Thirteen patients with a pathological diagnosis of glioblastoma multiforme were included in the study. Pathological preparations of each patient were analyzed retrospectively in histochemistry and immunohistochemistry laboratories. Transforming growth factor beta 1, TGF-beta 2, TGF-beta 3, Smad 1/2/3, Smad 6, and Smad 7 stainings were evaluated, and the immunoreactivity densities were examined. Result We found out an increase in the expression of TGF-beta 1 and TGF-beta 3 protein. Regarding the inhibitin receptors, Smad 6 showed much more expression than Smad 7. Thus, we found that Smad 6 has a protective effect and role in the tissue. Immunhistochemically, TGF-beta family stains, which are activated by types I-and -II receptors, and the stainless staining of the Smad family might also be showing that the TGF-beta family is taking action with a secondary pathway other than the Smad family. Conclusion In addition to Smad family receptors, Shc-GBR2, SARA, and Ras-Erk1/2 receptors should be investigated in future research. After that, the prognosis, diagnosis, and patient-based chemotherapy strategies for the treatment of glioblastoma multiforme may take a more prominent role.
引用
收藏
页码:134 / 144
页数:11
相关论文
共 17 条
[1]   TGF-βs and SMADs Activities at the Site of Failed Neural Tube in the Human Embryos [J].
Barutcuoglu, Mustafa ;
Umur, Ahmet Sukru ;
Vatansever, Hatice Seda ;
Umur, Nurcan ;
Ozbilgin, Kemal ;
Sayhan, Sevil ;
Selcuki, Mehmet .
TURKISH NEUROSURGERY, 2013, 23 (06) :693-699
[2]  
Bruce JN., 2009, GLIOBLASTOMA MULTIFO, V5
[3]   Evaluation of Ki-67 proliferation and apoptotic index before, during and after neoadjuvant chemotherapy for primary breast cancer [J].
Burcombe, Russell ;
D Wilson, George ;
Dowsett, Mitch ;
Khan, Ifty ;
Richman, Paul I. ;
Daley, Frances ;
Detre, Simone ;
Makris, Andreas .
BREAST CANCER RESEARCH, 2006, 8 (03)
[4]   CELL-KINETICS IN HUMAN BREAST-CANCER - COMPARISON BETWEEN THE PROGNOSTIC VALUE OF THE CYTOFLUOROMETRIC S-PHASE FRACTION AND THAT OF THE ANTIBODIES TO KI-67 AND PCNA ANTIGENS DETECTED BY IMMUNOCYTOCHEMISTRY [J].
GASPARINI, G ;
BORACCHI, P ;
VERDERIO, P ;
BEVILACQUA, P .
INTERNATIONAL JOURNAL OF CANCER, 1994, 57 (06) :822-829
[5]   Role of Cancer Microenvironment in Metastasis: Focus on Colon Cancer [J].
Gout, Stephanie ;
Huot, Jacques .
CANCER MICROENVIRONMENT, 2008, 1 (01) :69-83
[6]   TGF-β as a therapeutic target in high grade gliomas - Promises and challenges [J].
Joseph, Justin V. ;
Balasubramaniyan, Veerakumar ;
Walenkamp, Annemiek ;
Kruyt, Frank A. E. .
BIOCHEMICAL PHARMACOLOGY, 2013, 85 (04) :478-485
[7]   Glioma classification - A molecular reappraisal [J].
Louis, DN ;
Holland, EC ;
Cairncross, JG .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (03) :779-786
[8]   TGFβ in cancer [J].
Massague, Joan .
CELL, 2008, 134 (02) :215-230
[9]  
Platten M, 2001, MICROSC RES TECHNIQ, V52, P401, DOI 10.1002/1097-0029(20010215)52:4<401::AID-JEMT1025>3.0.CO
[10]  
2-C