Volume 27, Issue 4 (Autumn 2021)                   Intern Med Today 2021, 27(4): 550-565 | Back to browse issues page


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Gozali M, Ahmadizadeh C. Evaluation of Changes in NFKB Gene Expression Following Epstein-barr Virus and Its Participation in the Half-life of Patients With Acute Epstein-Barr Positive Lymphoblastic Leukemia. Intern Med Today 2021; 27 (4) :550-565
URL: http://imtj.gmu.ac.ir/article-1-3615-en.html
1- Department of Microbiology, Faculty of Basic Science, Ahar Branch, Islamic Azad University, Ahar, Iran.
2- Department of Microbiology, Faculty of Basic Science, Ahar Branch, Islamic Azad University, Ahar, Iran. , dr_ahmadizadeh@yahoo.com
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1. Introduction
Leukemia is one of the most common childhood malignancies, affecting about 40 cases per million children under 15. Acute Lymphoblastic Leukemia (ALL) accounts for about 75% of these cases. ALL is divided according to cell line into T or B. Signs and symptoms of acute leukemia are associated with normal tissues and can lead to bone marrow failure or specific tissue infiltration. Common symptoms are fever, paleness, petechia, ecchymosis, nausea, anorexia, and bone or joint pain [12]. Acute leukemia is the most common type of malignancy in children and accounts for about 30% of all childhood malignancies. Statistics show that 4 out of every 100000 children under the age of 15 have acute leukemia. About 77% of pediatric leukemia are acute lymphoblastic, 11% are myeloblastic, and 12% are other types of leukemia [3]. ALL is a type of white blood cell leukemia or cancer. ALL damages and kills normal bone marrow cells and spreads to other organs. Although the disease is most common in childhood between 2 and 5, it can also be seen in people over 60. In ALL, the precursors of B and T lymphocytes are involved. Mutations in proto-oncogenes and their conversion to oncogenes are effective factors in causing malignancies. ALL prevalence is higher in males than females [45]. 
Epstein-Barr Virus (EBV) is the first DNA tumor virus discovered and is a herpes virus family member. EBV consists of a dual-stranded genome approximately 172 kb in length that encodes more than 80 genes and unencoded RNAs. It is a linear virus but forms circular as an epizome in the nucleus of infected cells. EBV is associated with many malignant diseases of lymphoma carcinomas, as well as many benign diseases, such as infectious mononucleosis, and is also considered a promoter factor for some autoimmune diseases. In total, about 1%-1.5% of the cancers are estimated to be related to EBV worldwide [6]. 
The Epstein-Barr virus infects about 90% of the population and is the primary infection in young children, and may cause mononucleosis infection [7]. In most people, the virus is lodged in B cells, and the health consequences are not recognized. However, the virus has a list of associated malignant diseases of lymphoid or enveloping origin, such as Burkitt lymphoma, post-transplant lymphocytic disease, B immune lymphoma, Hodgkin’s lymphoma, natural killer T cell lymphoma, rhinoplasty, leiomyosarcoma in AIDS, and - * + gastric cancer subsets. In addition, these viruses are associated with areas, such as the chest, lungs, and prostate [8]. 
NF-κB is a protein complex that controls DNA transcription, cytokine production, and cell half-life. Its gene is expressed in most cells and changes its behavior under the influence of various environmental factors such as stress, viruses, and radiation. NF-κB is a major factor in regulating the pattern of immune response to microbial agents. Abnormal regulation of the NFKB gene has been observed in various diseases, such as cancers [9, 10]. NF-κB is a transcription factor that regulates the expression of antiapoptotic genes and activates chemokines and proinflammatory cytokines. NF-κB is a key mediator in carcinogenesis by inflammation [11]. NF-κB is widely used by eukaryotic cells to regulate the expression of genes involved in proliferation and survival. Therefore, many human tumors have abnormal and unregulated NF-κB, in which NF-κB is permanently active [12 ,13]. NF-κB activates the expression of genes that keep cell proliferation active and, on the other hand, protects cells against apoptosis. This transcription factor is involved in various cellular activities and plays an important role in various biological functions. Known actions of this factor include the regulation of immune and inflammatory responses, cell proliferation, hematopoiesis, and NFKB apoptosis. Takada et al. showed that TNF-induced apoptosis is potentiated by the suppression of NF-κB in acute human Jurkat cell leukemia [14]. Lehtinen et al. concluded that activation of maternal herpes virus infection increases the risk of ALL in children. Only positive EBV immunoglobulin in mothers, EBV-IgG, is associated with a significant risk of ALL in children [15]. Previous studies have shown that H2O2 is an effective inducer of NFκB pathway activation [16]. This study aimed to evaluate the increase in NFKB expression following the EBV virus and its participation in the half-life of EBV-positive acute lymphoblastic leukemia patients.
2. Materials and Methods
Statistical population

The sample size was estimated at 60 (60 healthy individuals as control and 60 patients with acute lymphoblastic leukemia) using the following formula considering P = 0.1, with a 95% confidence interval and a tolerable error rate of 0.04.


In this case-control study, we included the children aged 14 years with ALL who were referred to Tabriz Children’s Hospital, Tabriz City, Iran, in 2019. After referral, the details of each patient were recorded with the permission and consent of the patient. The inclusion criteria included patients with no history of acute viral infections, autoimmune diseases, or endocrine disorders. An oncologist confirmed the diagnosis of ALL in children. These patients were sampled before starting chemotherapy. Two milliliters of venous blood were taken from each individual and poured into the Falcon tubes, containing EDTA as an anticoagulant. Then, the tubes were gently shaken to mix and prevent blood clots from forming and eventually transferred to the laboratory and stored in a freezer at -80°C. In addition, the blood of 60 healthy individuals was taken as a control group.
RNA extraction
 To extract RNA, the cells were lysed with Traysol buffer. The resulting cell lysates were transferred into DNase/RNase-free microtubules. Then, 200 μL of chloroform was added to the microtube and centrifuged at 12000 rpm for 10 min. In the next step, the supernatant was discarded, and 70% isopropanol was added to it. On the next day, the tubes were centrifuged for 10 min at 12000 rpm, and then the supernatant was discarded, and the precipitate was dried at ambient temperature. Finally, the resulting precipitate was dissolved in 1 μL. The amount of RNA extracted by the optical method was measured using the NanoDrop device (Wilmington, DE, USA), and the quality of RNA was evaluated by gel electrophoresis.
Electrophoresis of extracted RNA samples
 To evaluate the quality of the extracted RNAs, 5 samples were electrophoresed randomly on the formaldehyde agarose gel. For this purpose, first, 0.8 gel was made. Then, the samples were loaded on the gel after tightening the gel and were electrophoresed at 80V for 1 hour. 
Quantitative RNA analysis
Quantitative analysis of RNA was performed by NanoDrop device with absorption measurements at 260 and 280 nm.
cDNA synthesis
The complementary DNA molecules were fabricated with the QuantiTect Reverse Transcription kit by Kiajen. The used primers were designed by Gene runner software (Version 3.05) and BLASTed by the NCBI website (www.ncbi.nlm.nih.gov). Table 1 presents the information on the primers.


The primers were synthesized by the Takapozist Company.
Real-time RT-PCR
A real-time PCR reaction was performed in triplicate. Thus, in real-time PCR tubes, 1 μL of cDNA and 19 μL of the Mastermix SYBR green, containing 1 μL of forwarding primer (0.2 μM), 1 μL of Primer Rivers (0.2 μM), 7 μL of DEPC, and 10 μL Mastermix 1x real-time were shed. Then the tubes were placed in real-time PCR, and the device was run.
Isolation of viral dna from a sample of patients with leukemia
To investigate the methylation of the NFKB gene, total DNA from the received paraffin block was isolated according to the instructions of Bioneer, the manufacturer of the DNA extraction kit from the paraffin block with catalog number 740980.50. To evaluate the methylation of the EBV virus genome, viral DNA was first isolated from tissue samples of EBV-positive acute lymphoblastic leukemia patients as follows. First, 200 mg of homogenized tissue was transferred into a 1.5 mL tube, then 200 μL of lysis buffer HL was added and incubated for 5 minutes at room temperature. Next, 20 μL of proteinase K and 20 μL of Carrier DNA were added and mixed. Then, the internal control of binding buffer HL was added to the amount and mixed. The mixture was transferred to an RTA Spin Filter and incubated for 1 min at room temperature. The mix was centrifuged at 2000 rpm for 2 min. The mixture was again transferred into the RTA Spin Filter into the new RTA Receiver.
Afterward, 500 μL of Wash Buffer I was added to the RTA Spin Filter. The mixture was centrifuged at 11000 rpm for 1 min. The mixture was again transferred to a new RTA Spin Filter. Next, 700 μL of Wash Buffer II was added and centrifuged. Then, the filter was removed and placed on the tube. The RTA Spin Filter was transferred to a new tube. It was centrifuged at maximum speed for 4 min to remove the ethanol completely. It was transferred to a new filter for 15 minutes. Then,100 μL of Elution Buffer, previously heated to 56°C was added to the RTA Spin Filter, and the mixture was incubated at room temperature for 1 min, then centrifuged and the viral DNA at 4°C or 20 °C stored.
Quantify the EBV Virus
The auxiliary standards in Kit ™ (DynaBio. Takapozist, Iran) were the same as the sample extraction method and with the same volume.
To generate a standard curve in RotorGene ™ 2000/3000/6000, all 5 standards were defined in the editing menu of RotorGene software. The same items were used as the standards for the specified concentrations.
The following formula was applied to convert the specified values using the standard curve to IU/mL samples.


Statistical analysis
After completing the laboratory work, using Hardy Weinberg’s law, the expected and observed frequencies were calculated and entered into the SPSS. Analysis of variance was used to compare the mean number of mutant alleles in the study population. The null hypothesis in ANOVA is that the mean of the dependent variable is equal at all levels of the independent variable.
3. Results
The patient group comprised 24 men (41.4%) and 36 women (58.6%), and the control group included 24 men (41.4%) and 36 women (58.6%). The Mean±SD age in the patient group was 8.6±1.35 years, and the mean age in the healthy group was 7.74±1.46 years. There was no statistical difference between the patient group and the healthy group regarding the mean age (Table 2).


Qualitative analysis of RNA
 To confirm the quality of the extracted RNA, electrophoresis of the samples was performed on 0.8% agarose gel, showing ribosomal 18s and 28s bands (Figure 1).

The presence and quality of ribosomal 18s and 28s bands indicate the quality of the extracted RNA.
Quantitative analysis of treated RNA
After treating the RNA extracted by the mentioned method and quantifying it, spectrophotometric analysis was performed to ensure their concentration.
Evaluation of NFKB Gene Expression Change in Leukemia Cells by Real-Time PCR
To evaluate NFKB expression change, after initial configuration, we performed RNA extraction. After cDNA synthesis, the expression pattern was examined using primers and specific probes.
Study of NFKB Gene Expression in Leukemia Cells Compared With the Control Samples by Real-Time RT-PCR
NFKB gene expression was evaluated in leukemia samples. The results showed that NFKB gene expression increased significantly in the group of acute lymphoblastic leukemia (P<0.05, Figure 2).

The result of changes in NFKB gene expression showed that the EBV virus decreased NFKB gene expression in EBV positive groups (P=0.041) (Figure 3).

Table 3 separately shows the significant pattern of the NFKB gene using the unpaired t-test.


4. Discussion
This study showed that the expression of the NFKB gene increased significantly in the patient group, and the Epstein-Barr virus decreased the expression of the NFKB gene in Acute Lymphoblastic Leukemia (ALL). ALL is a type of cancer that affects lymphocytes and lymphocyte-producing cells in the bone marrow. Lymphocytes are a type of white blood cell that produces antibodies and are vital parts of the immune system. Lymphocytes are divided into subgroups based on their functions, the most important of which are B and T cells. In ALL, an accumulation of cells that make up immature lymphocytes called blast cells is seen in the bone marrow. These cells affect normal blood cells and eventually reduce the production of red blood cells, white blood cells, and platelets. Acute Lymphoblastic Leukemia (ALL) is the most common malignancy in childhood, occurring in 80% to 85% of cases of children less than 6 years old [17]. In a 2004 study, Pui et al. found that neurological involvement was rare in patients with leukemia [18]. Also, in the study of Akramipour et al., who studied 5 years of children with acute myeloid leukemia in Ahvaz Shafa Hospital, less than 5.3% involvement of the nervous system in these patients was reported [19].
NFKB is a transcription factor that plays an important role in inflammation, immune responses, innate and acquired immunity by regulating various aspects of the evolution and function of functional cells, which is consistent with our study [20]. A study on liver HepG cells by Narayanan et al. revealed that in virus-infected cells, two types of reactive oxygen species increase, thereby activating the NF-κB pathway in the early stages of the disease. This finding is consistent with our study [21]. The results of Chinini’s study show that I3C and its compounds can induce apoptosis in various cancer cells by inhibiting the NF-κB transcription factor, which is inconsistent with our study [22]. Salvatore et al., in their research, stated that following treatment of cells with doxorubicin, this compound inhibits DNA synthesis by binding to double-stranded DNA and stabilizing the topoisomerase II complex, leading to the induction of apoptosis.
On the other hand, in addition to this process, another pathway is activated, which, by using NF-κB and subsequent activation of genes involved in cell survival such as survivin, IAP1-c, and XIAP, prevents cell death. These results are consistent with our study [23]. The results of a study by Adcock et al. showed that NF-κB activation plays an important role in inflammatory processes, immune responses, and cell death through binding to promoters of various genes such as TNF-α, 1β-IL, and cyclooxygenase-2. This finding is not consistent with our study [24]. Go et al. stated that valproate protects neurons from oxidative stress-inducing cell death by increasing NF-κB acetylation and has a neuroprotective effect consistent with our study [25]. In the study of intermediate proteins, 170 related protein kinases were observed from the expressed reduced genes, of which 62 were predicted to be specific for the expressed reduced genes, and among 62 kinases (Inhibitor of NF-κB), kinase subunit (Beta) IKBKB received the best score. It plays an important role in the NF-κB signaling pathway activated in DNA damage, cytokine inflammation, bacterial and viral production. By activating hundreds of genes, it triggers the immune response, growth control, and protection against apoptosis. This finding is consistent with our study [26]. Rothe stated in his research that some molecules whose expression is regulated in EBV-infected cells might play an indirect role in NF-κB activation. SNK6 cells are reported to produce TNF-α, which activates NF-κB in T and NK cells [27]. Rothe stated in his study that NF-κB could be activated downstream of CD40 and CD137. EBV-induced CD40 or CD137 expression may be involved in NF-κB activation in EBV-T/NK cells. This result is not consistent with our study [27]. Sugano et al. reported that EBV binding initiates NF-κB activation, which is necessary for successful cell infection. NF-κB activity, in turn, also regulates the expression of the CD21 molecule, which may provide a positive feedback loop to enhance cell sensitivity to EBV entry. This finding is inconsistent with our study [28]. Cahir-McFarland et al. showed that deletion of NF-κB activity-induced apoptosis of EBV-infected lymphoma cell lines in vitro and mice, indicates that this is a major pathway created by viral oncoproteins. The findings are consistent with our study results [29, 30]. There is a relationship between NF-κB activation and cell proliferation in cell cycle arrest based on the relative balance between biological and biochemical functions of NF-κB, besides the important role of NF-κB in resistance to apoptosis and hematopoietic stem cell division control. Recently NF-κB has also been shown to be involved in oxidative stress. NF-κB activation is responsible for activating Nitric Oxide Synthase (iNOS) to increase Nitric Oxide (NO), described as a pro-apoptotic function of NF-κB. Nitric oxide production pattern may control cell survival because acute NO production has been shown to cause apoptosis. However, chronic NO production with active constituent NF-κB signaling can inhibit the mechanism of apoptosis. This finding is consistent with our study [31]. Safa et al. reported that in human tumorigenesis, NFKB is an essential factor in the survival of cancer cells, which is consistent with our study [31]. Poglio et al. reported that changes in the NF-κB pathway are recognized, particularly in ALL and other types of leukemia. For example, its regulation should facilitate leukemia cell apoptosis. This finding is consistent with our study [32]. A study published by Lehtinen et al. showed that maternal reactivation of EBV infection in the first trimester was associated with a significant increase in the incidence of ALL in offspring. This result is inconsistent with our study [15]. Takada et al. showed that TNF-induced apoptosis is amplified by the suppression of NF-κB in acute human Jukart cell leukemia. This result is consistent with our study [14].
5. Conclusion
The NFKB gene could be a precursor to the diagnosis of acute lymphoblastic leukemia. However, further studies on EBV infection and acute lymphoblastic disease are required.

Ethical Considerations
Compliance with ethical guidelines

Informed consent was obtained from patients and families participating in the current study.

Funding
This article was extracted from MA. thesis of the first author at the Department of Microbiology, Faculty of Basic Science, Ahar Branch, Islamic Azad University, Ahar, Iran.

Authors' contributions
All authors contributed to the current article, equally.

Conflicts of interest
The authors declared no conflict of interest.
 

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Type of Study: Original | Subject: Basic Medical Science
Received: 2020/11/21 | Accepted: 2021/02/27 | Published: 2021/10/1

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