HSOA Journal of Addiction & Addictive Disorders Epidermal Growth Factor Receptor Expression Analysis in Different Racial Glioma Patients

Epidermal Growth Factor Receptor Expression Analysis in Different Racial Glioma Patients. Abstract Background Vascular Endothelial Growth Factor (VEGF) represents a prom-ising anti-neoplastic target. VEGF expression in same pathological grade of glioma in different ethnicities patients has not been inte-grated into clinical practice yet. The aim of our study is to investigate the relationship between VEGF expression level and prognosis in different ethnicities patients with glioma of


Introduction
Glioma is the most common primary tumors of the brain in adults [1]. The 5-year survival rate in patients with glioma is surprisingly low [2]. Conventional therapies play an important role in the treatment of malignant gliomas. However, the prognosis for patients with malignant gliomas still leaves much to be desired. In recent years, there have been some renewed efforts to develop the novel treatments based on molecular targets of glioma. The identification of these factors that can predict survival is an important goal for treatment of these patients, and a large number of studies have shown that the expression of VEGF was obviously related to the pathological grade of the tumor [3][4][5][6][7]. However, in a review of the literatures, no studies reported the association between VEGF expression level and different ethnic populations with an identical pathological classification. In this study, we compared the difference in VEGF expression level in glioma patients with identical classifications who settled in the Xinjiang province of China to elucidate whether ethnicity affects the VEGF expression and prognosis of these patients.

Methods
Tumor specimens were tested by immunohistochemistry for VEGF expression level using the Dako Epidermal Growth Factor Receptor (EGFR) pharm Dx assay™ (Dako, Denmark). VEGF expression level immunostaining score was calculated as the percentage of positively stained tumor cells and the staining intensity. A nucleus dyeing rate of 0~9% was marked as+, 10%~49% [2+] and >50% [3+] [8]. Both the percentage of positive cells and the staining intensity were evaluated under double-blind conditions. Two independent pathologists examined and scored each sample without any knowledge of the pathological outcome. The VEGF expression score was calculated as the percentage positive score × the staining intensity score and ranged from 0 to 9. SPSS 20.0 was used in all statistical analyses. Numerical variables were summarized as an mean (standard deviation) or median (interquartile range). For comparison between the two groups, categorical variables were analyzed via the chi-square test. To elaborate the relationship between glioma VEGF expression level and pathological grades in the two ethnicities, the contingency table test was employed. Significance was defined as a P value of <0.05.

VEGF expression level in Uygur and Han glioma patients
Positive VEGF expression rate in the tumor tissues in Han and Uygur glioma patients were 81.97% and 60.61%, respectively. When the positive rate of VEGF expression in the two groups was compared and analyzed, the expression difference was statistically significant (P=0.023). The VEGF expression level in Uygur patients was obviously lower than that in Han patients, which demonstrated that ethnicity can affect VEGF expression in glioma patients ( Table 1).

The correlation between the pathological grade and VEGF expression level in Han glioma patients
We analyzed the association between pathological grade and VEGF expression level in Han glioma patients. The result showed that the VEGF expression level in Han glioma patients was significantly related with tumor pathological classification (P=0.024) ( Table  2). Table 3 displays the relationship between the pathological grade and VEGF expression level of 33 Uygur glioma patients. The results indicated that the VEGF expression level in Uygur glioma patients was not significantly different from the tumor pathological grade (P=0.683).

Survival analysis between Uygur and Han glioma patients with identical pathological grade
In patients with grade I and II glioma, the median survival was62 months in Han people (22 cases) and 69 months in Uygur people (9 cases). There was no statistical difference between the two groups (P=0.125), namely, the survival time of LGG patients has no obvious relationship with ethnicity ( Figure 1).    In glioma patients with grade III, the median survival was 16.2 months in the Han group (25 cases) and 28.7 months in the Uygur group (10 cases). There was a significant difference between the two groups (P=0.007). The average survival time of Uygur patients with grade III glioma was longer than that of Han patients (Figure 2).
In patients with grade IV glioma, the median survival time was 11.8 months in the Han group (14 cases) and 17.5 months in the Uygur group (13 cases).There was a significant difference between the two groups (P=0.007). The survival time of Uygur glioma patients with grade IV glioma was longer that of Han patients (Figure 3).

Discussion
Vascular endothelial growth factor can induce angiogenesis, increase vascular permeability and promote division and proliferation of vascular endothelial cell [9]. VEGF also plays a key role in the process of tumor growth [10]. The vascular endothelial growth factor family of polypeptide growth factors regulates a family of VEGF receptor tyrosine kinases with pleiotropic downstream effects [4]. Angiogenesis is the best known of these effect Angiogenesis leads to new blood vessel formation and is implicated in both physiological and pathological situations [7]. The vascular endothelial growth factor family is the major mediator of this process. in patients with classical Hodgkin lymphoma (cHL), the level of VEGF-A, VEGFR-1 and VEGFR-2 was tested, only the expression of VEGFR-2 was positively correlated with serum albumin levels ≥4g/dL. No correlation with patient outcome was observed in CHL patients [4]. The T allele of VEGF +936C/T polymorphism is more common in primary tumors of the glioma, but there is no statistical relation with survival [5]. Angiogenesis commonly attributed to the anticrime and paracrine production of VEGF-A, which up regulates the VEGF signal transduction pathway, is a prominent feature of glioblastoma [11]. VEGF is secreted more in the glioma tissue than in normal brain tissue [12,13]. In recent years, the targeted molecular therapy of glioma based on VEGF as the target has gradually become a new strategy [14]. A large number of studies have indicated that VEGF expression level in glioma was closely related to the degree of malignancy of the tumor [15]. The higher the tumor pathological grade is, the higher the level of VEGF expression is [16,17]. Sometimes, The level of expression of some tumor related factors in tumors is closely related to the malignancy of tumors and the prognosis of tumors in Chinese just as Neutrophil-to-Lymphocyte Ratio (NLR) and Platelet-To-Lymphocyte Ratio (PLR) in the glioma, increased preoperative NLR and PLR are associated with worse OS, and NLR may be an independent risk factor to identify glioma patients with poor prognosis [18].
In the present study, we performed VEGF immunohistochemical staining on the embedded paraffin specimens. The positive rate of VEGF expression in Han patients was significantly correlated with tumor pathological grade, which was by and large consistent with other studies [19]. However, the difference was that positive VEGF expression rate in Uygur patients was remarkably lower than that in Han patients. Nonetheless, there was no obvious relationship between pathological grade in the Uygur glioma patients and the VEGF expression level, but the pathological grade was positively associated with VEGF expression level. We surmised that the negative result was possibly associated with the limited number of Uygur patients. Additionally, the VEGF expression level in HGG was distinctly high compared with that in LGG, which implied that the VEGF expression level may be considered as an index of the glioma grade.
When the ethnicity factor was analyzed for patients with gliomas of different pathological grades, there was no obvious difference regarding the role of ethnicity in the survival of LGG patients. However, this difference was evident between Han and Uygur patients with HGG. Thus, ethnicity is one factor impacting the survival in HGG patients.
Many studies confirmed that VEGF is highly expressed in tumor tissue. Xi observed that the rate of positive VEGF expression was positively correlated with pathological grade, the rate of the positive expression in the higher grade group was higher than that in the lower grade group and the rate of positive expression in the invasive cancer group was higher than that in the superficial tumor group in bladder cancer [20]. These findings indicated that the expression of VEGF might be associated closely with the invasiveness, metastasis and other  biological traits of bladder cancer. Some researchers discovered that the expression of VEGF in esophageal carcinoma was associated with lymphatic metastasis and the depth of invasion, and the expression was lower in para-carcinoma tissues than in esophageal cancer tissues [21]. Many scholars have put forward different opinions about whether the expression of VEGF was related to the clinical characteristics of endometrial diseases. For example, Abulafiao thought there was no correlation between vasculogenesis and the tumor grade, but Nakayama had the opposite opinion [22,23]. They considered that there was no correlation between angiogenesis and other clinical pathological parameters, and that angiogenesis was related to tumor grade, but some study found that Genetic variants were not associated with gliomas. Specific lifestyle habits and comorbidities stood out as independent risk factors for the disease. Low-grade gliomas showed an increase in patient survival with TMZ+RT treatment [24,25].
Similar ethnicity-related target expression was tested for other molecular targets such as the EGFR [7,26]. However, several phase III trials comparing EGFR inhibitor-gefitinib to placebo in advanced non small cell lung cancer patients demonstrated no improvement in overall survival in an unselected population [27,28]. Asian patients achieved a statistically significant improvement in overall survival with gefitinib. Regarding the mechanism, patients who benefited from gefitinib tended to harbor somatic activating mutations in the EGFR gene [29,30]. These data illustrated that molecular mutations could be used to identify subgroup of patients to differentiate VEGF expression in Han and Uygur patients. Additionally, initial studies that analyzed the efficacy of bevacizumab with recurrent glioblastoma explained its clinical activity, and first-line use of bevacizumab did not improve overall survival, although progression-free survival was prolonged [30]. As a result, we conferred that the VEGF expression level determined the response of bevacizumab and led to the different efficacy.
There was a significant difference in the correlation of VEGF expression level and tumor pathological grade between Xinjiang Uygur and Han patients with glioma. We reckon that the cause of the difference is due to ethnicity. Due to this inconsistency, further study in a large series is required to determine whether there is a difference in the curative effect of the molecular targeted therapy for glioma based on VEGF as the target in Xinjiang Uygur and Han glioma patients.

Conclusion
The present study reveals a significant difference in VEGF expression levels in glioma tissue between Uygur and Han glioma patients, although the number of patients in our series is limited and the monitoring method might be responsible for the difference in VEGF expression in glioma tissue. It is crucial to analyze the difference in efficacy of bevacizumab as a targeted VEGF inhibitor in Han and Uygur glioma patients in future.