Evaluation of rs1957106 Polymorphism of NF-κBI in Glioblastoma Multiforme in Isfahan, Iran
Yasaman Sadeghi1, Pouya Tabatabaei Irani1, Laleh Rafiee2, Mohamadhasan Tajadini3, Shaghayegh Haghjooy Javanmard2
1 Department of General Medicine, Isfahan Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
2 Department of Applied Physiology Research Center, Isfahan Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
3 Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
|Date of Web Publication||31-Jan-2019|
Prof. Shaghayegh Haghjooy Javanmard
Applied Physiology Research Center, Isfahan Cardiovascular Research Institute, Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan
Source of Support: None, Conflict of Interest: None
Background: The kB family of nuclear factor (NF-κB) is a series of transcription factors that plays a key role in regulation of immunity, cell growth, and apoptosis and is considered as the main downstream component of epidermal growth factor receptor for which there are evidence of excessive activity in most cases of glioblastoma multiform (GBM). Thus, the current information has gained evidence on NF-κBIA tumor suppressor role in GMB. SNP rs1957106 was diagnosed as a new polymorphism which affected the expression of NF-κBI and causes activation of NF-κB in GBM patients. Materials and Methods: This study was conducted on 100 cases of GBM including 47 paraffin-embedded brain tissue samples and 53 blood samples from another 53 GBM patients and 150 controls. The NF-κBI rs1957106 SNP was identified by the NCBI, and genotyping was performed by high-resolution melt (HRM) assay. Melt curves from HRM which suspected to single-nucleotide polymorphism (SNP) were selected and subjected to direct sequencing. Results: The distribution of allele A of NF-κβ gene in patients with GBM with 31% was not significantly different from healthy participants (27.3%) (P = 0.375). Furthermore, the distribution of AG and GG genotypes in comparison with AA genotypes did not show a significant correlation with GBM incidence (P > 0.05). Conclusion: Findings of the present study provide evidence that the rs1957106 SNP in NF-κBIA is found more in GBM patients, but it was not statistically significant. As there are conflicting studies showing significant higher rate of this SNP in GBM, further study is suggested.
Keywords: Glioblastoma, NF-κBI, polymorphism
|How to cite this article:|
Sadeghi Y, Tabatabaei Irani P, Rafiee L, Tajadini M, Haghjooy Javanmard S. Evaluation of rs1957106 Polymorphism of NF-κBI in Glioblastoma Multiforme in Isfahan, Iran. Adv Biomed Res 2019;8:9
|How to cite this URL:|
Sadeghi Y, Tabatabaei Irani P, Rafiee L, Tajadini M, Haghjooy Javanmard S. Evaluation of rs1957106 Polymorphism of NF-κBI in Glioblastoma Multiforme in Isfahan, Iran. Adv Biomed Res [serial online] 2019 [cited 2019 Jul 19];8:9. Available from: http://www.advbiores.net/text.asp?2019/8/1/9/251214
| Introduction|| |
Glioblastoma (GBM) is the most common and invasive form of primary malignant brain tumors with a survival rate of about 1 year.,, Low survival rates have led to provide a treatment method in order to tumor removal or increase survival in GBM, and unlike the current treatment regimens, GBM survival of 5 years has still been reported to be <10%.,,
This cancer has a poor prognostic as well as its molecular mechanisms are less known.,
Many studies have shown that a number of signaling pathways would be unregulated during the multistage GMB carcinogenesis,,,,,, and there are evidence of excessive activity of epidermal growth factor receptor (EGFR) in the most cases of GMB. The κB family of nuclear factor (NF-κB) is a series of transcription factors that plays a key role in regulation of immunity, inflammatory responses, cell growth, and apoptosis and is considered as the main downstream component of EGFR, which consists of a group of homodimer and heterodimer protein complexes;, among them, the heterodimer complex of p50/p65/p53 is the most common complex in many types of cells.,
In nonstimulated cells, the inactive NF-κB complex is present in the cytoplasm and has been bind to a variety of NF-κB inhibitor proteins called NF-κBI, including NF-κBIA, NF-κBIB, IKBγ, IKBε, bc1-3, p100, and p150. In many cases, NF-κB activation is performed with NF-κBIA signal induced destruction, and as a result, the transcription factor is released and transferred to the nucleus.,, The family of NF-κBI proteins is characterized by the presence of multiple ankyrin repeats and their ability to physical connection to NF-κB proteins. Among this family, NF-κBIA has three sections: the N-terminal section, which has phosphorylation sites and is involved in degradation regulation, the ankyrin repeat section, and the C-terminal PEST section that controls the basic degradation.,,,,
Mutations, polymorphisms, and NF-κBIA haplotype have been reported in Hodgkin's lymphoma, colorectal cancer, melanoma, hepatocellular carcinoma, breast cancer, and multiple melanomas,,,,,,,,,,,,, as well as an inappropriate structural activation of NF-κB has been reported in GMB.,,, In addition, the current information has gained evidence on NF-κBIA tumor suppressor role in GMB.
In addition, GMB cells that did not respond to chemotherapy were found to have lower mRNA expression, and increased expression of NF-κBIA inhibited tumor malignancy. These results suggest that this single-nucleotide polymorphism (SNP) can be used to predict the survival rate of the affected patients. From the limited impact of EGFR target treatment in GMB, it can be understood that the effect of EGFR inhibitor treatment may be reduced by interfering transmission pathways, mutation, or augmentation of growth factor receptors such as PDGR, PDGFRA, ERBB2, or MET. Because NF-κBIA is the main downstream factor in these transmission pathways, NF-κBIA-stabilizing treatments can be much more effective in controlling oncogenic pathways.
Given the evidence presented in our report on SNP rs1957106, this study was aimed to find a way to better prognosis and treatment for patients with malignant tumor GBM by examining this polymorphism in cancerous specimens that still have unspecified aspects.
| Materials and Methods|| |
This case–control study was approved by the Research and Ethics Committee of Isfahan University of Medical Sciences. After providing sufficient information, a written consent was obtained from all participants or their legal guardians before involvement in the project. This study was conducted on 100 cases of GBM including 47 paraffin-embedded brain tissue samples that were taken from the Department of Pathology of Alzahra University Hospital and 53 blood samples from another 53 GBM patients, who were under therapy for this disease from Milad Hospital, and 150 controls from population of Isfahan, Iran, from 2013 to 2015.
DNA was extracted from brain tissue samples using PFET-DNA extraction kit (Yektatajhiz Inc., Tehran, Iran) and from blood samples using blood-DNA extraction kit (Yektatajhiz Inc., Tehran, Iran) according to the manufacturer's protocol.
The NF-κBI rs1957106 SNP was identified by the NCBI, and ensemble databases and primers were designed by Beacon Designer 8.1 ((Premier Biosoft International, USA) and synthesized by Bioneer (Bioneer, Korea). The forward primer was 5′-sequence-3′ and reverse primer was 5′-sequence-3′. Genotyping was performed by high-resolution melt (HRM) assay using a Rotor-Gene 6000 instrument (Corbett Life Science, Australia) [Figure 1] and [Figure 2].
Polymerase chain reaction (PCR) reactions were carried out in triplicate in 10 μL of final volume using the type-it HRM kit (Qiagen, Germany) according to the manufacturer's protocol. The PCR program consisted of an initial denaturation-activation step at 95°C for 10 min, followed by a 40-cycle program (denaturation at 95°C for 15 s, annealing conditions 60°C for 20 s, 72°C for 20 s; an HRM step from 75°C to 95°C rising at 0.1°C/s). Curves for each triplicate were checked on the shape, melting pattern, and Tm to meet reproducibility.
Melt curves from HRM which suspected to SNP were selected and subjected to direct sequencing.
The Hardy–Weinberg equilibrium (HWE) was tested to compare the observed genotype frequencies with the expected frequencies among samples, so that the genotype distribution of NF-κβ rs1957106 was compatible with the HWE in our patients.
Finally, the collected data were entered into the SPSS software (version 20; SPSS Inc., Chicago, Ill., USA), and mean ± standard deviation or n (%) was used to show the data. Moreover, Fisher's exact test and independent t-test were applied for statistical analysis of frequency distribution of gender and mean age. To show the relationship between the genotype, NF-κβ I rs1957106 allele, and GBM disease, logistic regression was used and odds ratio was reported. Furthermore, to increase the precision of the study, variables such as age and gender were taken under control as the confounding variables. In all the analyses, P < 0.05 was considered statistically significant.
| Results|| |
In the present study, in the control group, 150 healthy individuals consisting of 80 (53.3%) males and 70 (46.7%) females were enrolled. The mean age of the control group was 49.67 ± 15.12 years. Meanwhile, in the case group, 100 patients with GBM including 55 (55%) males and 45 (45%) females were assigned. The mean age in this group was 51.63 ± 13.27 years. Accordingly, the two groups were matched in terms of age and gender (P > 0.05) [Table 1].
On the other hand, the distribution of allele A of NF-κβ gene in patients with GBM with 31% was not significantly different from healthy participants (27.3%) (P = 0.375).
Furthermore, the distribution of AG and GG genotypes in comparison with AA genotypes did not show a significant correlation with GBM incidence (P > 0.05). In addition, by controlling the age and sex, there was still no association between the allele and genotype of NF-κβ rs1957106 with GBM [Table 2].
|Table 2: Genotype and allele frequencies of nuclear factor-Kβ rs1957106 in two groups|
Click here to view
| Discussion|| |
Genetic polymorphisms in NF-κBI gene are noticed due to their role in Hodgkin's lymphoma, colorectal cancer, melanoma, hepatocellular carcinoma, breast cancer, and multiple myelomas.,,,,,,,,,,,, In this study, we analyzed the alterations of this gene in GBM. We analyzed the DNA sequence of the NF-κBIA gene from blood samples taken from 100 GBM patients and 100 noncancerous controls who were adjusted for sex and age.
It is to be noted that the prevalence of GBM was higher in men and its mean age was 51.63 ± 13.27 years. Thus, it can be concluded by adding other epidemiologic results that generally the GBM is more prevalent in men and it mostly occurs in elderlies rather than the youth.
On the other hand, the analysis of association of allele and genotype of NF-κBI gene with the occurrence of GBM showed that despite the frequency of A allele or AG and AA genotype was higher in GBM patients, this relation was not statistically significant. Furthermore, the presence of A allele was more frequent than G allele in these patients, and also, AG and AA genotypes had higher frequency rates that the difference was not significant. These results remained unchanged by adding sex and age as confounding variables, so we may conclude that sex or age did not have a role in the presence of this allele of genotype in these patients.
Accordingly, in the study of Zhao et al., they studied on the association between different genotypes of the NF-κBIA rs1957106 SNP and the gene copy number, mRNA level, and protein expression of NF-κBIA. The SNP rs1957106 AG and AA genotypes were associated with lower NF-κBIA protein levels and a poor prognosis of GBM patients. They revealed that the SNP rs1957106 AG and AA genotypes in GBM were associated with a comparatively shorter survival rate. Thus, their results suggest a role for NF-κBIA in the suppression of GBM tumors. Their results were in agreement with Bredel et al., who showed that a higher NF-κBIA expression was associated with a longer survival by studying bigger sample size of patients.
The study of Zhao et al. on 24 GBM patients and 8 controls showed SNP rs1957106 as a newly diagnosed polymorphism of NFKBI gene. Thus the conflict of our results may be due to fewer samples studied in the research of Zhao et al. comparing to 100 samples of GBM and 150 noncancerous patients in our study.
Finally, it might be necessary to say that one of the limitations of this study was difficulties in gathering GBM samples, because larger samples may lead to more reliable results. Furthermore, another weakness of our study was the lack of other clinical features and comorbid disease of these patients. Thus, the duration of disease, family history of GBM, and other comorbid diseases might affect the distribution of mentioned allele or genotypes in these patients. Hence, further study noticing these factors in a bigger sample size is recommended.
| Conclusion|| |
To the best of our knowledge, the results of the present study support that the rs1957106 SNP in NF-κBIA is found more in GBM patients, but it was not statistically significant. As there are conflicting studies showing significant higher rate of this SNP in GBM, further study is suggested.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Buckner JC. Factors influencing survival in high-grade gliomas. Semin Oncol 2003;30:10-4.
Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJ, et al.
Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med 2005;352:987-96.
Wen PY, Kesari S. Malignant gliomas in adults. N Engl J Med 2008;359:492-507.
DeAngelis LM. Brain tumors. N Engl J Med 2001;344:114-23.
Walker MD, Green SB, Byar DP, Alexander E Jr., Batzdorf U, Brooks WH, et al.
Randomized comparisons of radiotherapy and nitrosoureas for the treatment of malignant glioma after surgery. N Engl J Med 1980;303:1323-9.
Parsa AT, Waldron JS, Panner A, Crane CA, Parney IF, Barry JJ, et al.
Loss of tumor suppressor PTEN function increases B7-H1 expression and immunoresistance in glioma. Nat Med 2007;13:84-8.
Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Burger PC, Jouvet A, et al.
The 2007 WHO classification of tumours of the central nervous system. Acta Neuropathol 2007;114:97-109.
Lv S, Zhang J, Han M, Wang W, Zhang Y, Zhuang D, et al.
Nucleolin promotes TGF-β signaling initiation via TGF-β receptor I in glioblastoma. J Mol Neurosci 2015;55:1-6.
Parsons DW, Jones S, Zhang X, Lin JC, Leary RJ, Angenendt P, et al.
An integrated genomic analysis of human glioblastoma multiforme. Science 2008;321:1807-12.
Yan H, Parsons DW, Jin G, McLendon R, Rasheed BA, Yuan W, et al.
IDH1 and IDH2 mutations in gliomas. N Engl J Med 2009;360:765-73.
Phillips HS, Kharbanda S, Chen R, Forrest WF, Soriano RH, Wu TD, et al.
Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis. Cancer Cell 2006;9:157-73.
Bredel M, Scholtens DM, Harsh GR, Bredel C, Chandler JP, Renfrow JJ, et al.
A network model of a cooperative genetic landscape in brain tumors. JAMA 2009;302:261-75.
Yadav AK, Renfrow JJ, Scholtens DM, Xie H, Duran GE, Bredel C, et al.
Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas. JAMA 2009;302:276-89.
McLendon R, Friedman A, Bigner D, Van Meir EG, Brat DJ, Mastrogianakis GM. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 2008;455:1061-8.
Watanabe K, Tachibana O, Sata K, Yonekawa Y, Kleihues P, Ohgaki H, et al.
Overexpression of the EGF receptor and p53 mutations are mutually exclusive in the evolution of primary and secondary glioblastomas. Brain Pathol 1996;6:217-23.
Bargou RC, Leng C, Krappmann D, Emmerich F, Mapara MY, Bommert K, et al.
High-level nuclear NF-kappa B and oct-2 is a common feature of cultured Hodgkin/Reed-Sternberg cells. Blood 1996;87:4340-7.
Grüssel T, Busch W. Experimental studies of the effect of peracetic acid on the endometrium of cattle. Tierarztl Pra×1997;25:28-34.
Barkett M, Gilmore TD. Control of apoptosis by Rel/NF-kappaB transcription factors. Oncogene 1999;18:6910-24.
May MJ, Ghosh S. Signal transduction through NF-kappa B. Immunol Today 1998;19:80-8.
Chiao PJ, Miyamoto S, Verma IM. Autoregulation of I kappa B alpha activity. Proc Natl Acad Sci U S A 1994;91:28-32.
Baeuerle PA, Baltimore D. NF-kappa B: Ten years after. Cell 1996;87:13-20.
Matthews JR, Nicholson J, Jaffray E, Kelly SM, Price NC, Hay RT, et al.
Conformational changes induced by DNA binding of NF-kappa B. Nucleic Acids Res 1995;23:3393-402.
Roulston A, Lin R, Beauparlant P, Wainberg MA, Hiscott J. Regulation of human immunodeficiency virus type 1 and cytokine gene expression in myeloid cells by NF-kappa B/Rel transcription factors. Microbiol Rev 1995;59:481-505.
Jacobs MD, Harrison SC. Structure of an IkappaBalpha/NF-kappaB complex. Cell 1998;95:749-58.
Spink CF, Gray LC, Davies FE, Morgan GJ, Bidwell JL. Haplotypic structure across the I kappa B alpha gene (NFKBIA) and association with multiple myeloma. Cancer Lett 2007;246:92-9.
Krappmann D, Emmerich F, Kordes U, Scharschmidt E, Dörken B, Scheidereit C, et al.
Molecular mechanisms of constitutive NF-kappaB/Rel activation in Hodgkin/Reed-sternberg cells. Oncogene 1999;18:943-53.
Cabannes E, Khan G, Aillet F, Jarrett RF, Hay RT. Mutations in the ikBa gene in hodgkin's disease suggest a tumour suppressor role for ikappaBalpha. Oncogene 1999;18:3063-70.
Zhao Z, Zhong X, Wu T, Yang T, Chen G, Xie X, et al.
Identification of a NFKBIA polymorphism associated with lower NFKBIA protein levels and poor survival outcomes in patients with glioblastoma multiforme. Int J Mol Med 2014;34:1233-40.
Emmerich F, Meiser M, Hummel M, Demel G, Foss HD, Jundt F, et al.
Overexpression of I kappa B alpha without inhibition of NF-kappaB activity and mutations in the I kappa B alpha gene in Reed-Sternberg cells. Blood 1999;94:3129-34.
Jungnickel B, Staratschek-Jox A, Bräuninger A, Spieker T, Wolf J, Diehl V, et al.
Clonal deleterious mutations in the IkappaBalpha gene in the malignant cells in Hodgkin's lymphoma. J Exp Med 2000;191:395-402.
Lake A, Shield LA, Cordano P, Chui DT, Osborne J, Crae S, et al.
Mutations of NFKBIA, encoding IkappaB alpha, are a recurrent finding in classical Hodgkin lymphoma but are not a unifying feature of non-EBV-associated cases. Int J Cancer 2009;125:1334-42.
Sjöblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, et al.
The consensus coding sequences of human breast and colorectal cancers. Science 2006;314:268-74.
Gao J, Pfeifer D, He LJ, Qiao F, Zhang Z, Arbman G, et al.
Association of NFKBIA polymorphism with colorectal cancer risk and prognosis in Swedish and Chinese populations. Scand J Gastroenterol 2007;42:345-50.
Osborne J, Lake A, Alexander FE, Taylor GM, Jarrett RF. Germline mutations and polymorphisms in the NFKBIA gene in Hodgkin lymphoma. Int J Cancer 2005;116:646-51.
He Y, Zhang H, Yin J, Xie J, Tan X, Liu S, et al.
IkappaBalpha gene promoter polymorphisms are associated with hepatocarcinogenesis in patients infected with hepatitis B virus genotype C. Carcinogenesis 2009;30:1916-22.
Bu H, Rosdahl I, Sun XF, Zhang H. Importance of polymorphisms in NF-kappaB1 and NF-kappaBIalpha genes for melanoma risk, clinicopathological features and tumor progression in Swedish melanoma patients. J Cancer Res Clin Oncol 2007;133:859-66.
Liu X, Yu H, Yang W, Zhou X, Lu H, Shi D, et al.
Mutations of NFKBIA in biopsy specimens from Hodgkin lymphoma. Cancer Genet Cytogenet 2010;197:152-7.
Parker KM, Ma MH, Manyak S, Altamirano CV, Tang YM, Frantzen M, et al.
Identification of polymorphisms of the IkappaBalpha gene associated with an increased risk of multiple myeloma. Cancer Genet Cytogenet 2002;137:43-8.
Raychaudhuri B, Han Y, Lu T, Vogelbaum MA. Aberrant constitutive activation of nuclear factor kappaB in glioblastoma multiforme drives invasive phenotype. J Neurooncol 2007;85:39-47.
Nagai S, Washiyama K, Kurimoto M, Takaku A, Endo S, Kumanishi T, et al.
Aberrant nuclear factor-kappaB activity and its participation in the growth of human malignant astrocytoma. J Neurosurg 2002;96:909-17.
Tsunoda K, Kitange G, Anda T, Shabani HK, Kaminogo M, Shibata S, et al.
Expression of the constitutively activated RelA/NF-kappaB in human astrocytic tumors and the in vitro
implication in the regulation of urokinase-type plasminogen activator, migration, and invasion. Brain Tumor Pathol 2005;22:79-87.
Bredel M, Scholtens DM, Yadav AK, Alvarez AA, Renfrow JJ, Chandler JP, et al.
NFKBIA deletion in glioblastomas. N Engl J Med 2011;364:627-37.
[Figure 1], [Figure 2]
[Table 1], [Table 2]