High vimentin expression with E-cadherin expression loss predicts a poor prognosis after resection of grade 1 and 2 pancreatic neuroendocrine tumors

Background Pancreatic neuroendocrine tumors (pNETs) are a heterogeneous group of neoplasms with malignant behaviors that can develop from inert slow growth or low malignancy to aggressive metastasis during follow-up. Recently, vimentin and E-cadherin were shown to be prognostic markers in some malignant tumors but were not evaluated in pNETs. The aim of this study was to evaluate the expression and prognostic significance of vimentin and E-cadherin in grade 1 and 2 pNETs. Methods A retrospective review of 227 patients with grade 1 and 2 pNETs undergoing surgical resection was conducted. Tumor specimens were immunohistochemically stained for vimentin and E-cadherin. Correlations between vimentin and E-cadherin expression and other clinicopathological features were then analyzed. Furthermore, overall survival (OS) and disease-free survival (DFS) were evaluated using Kaplan-Meier and univariate and multivariate Cox regression methods. Results Among 227 patients, 55 (24.2%) harbored tumors with high vimentin expression, while 117 (51.5%) harbored tumors with loss of E-cadherin expression. Patients with high vimentin expression and loss of E-cadherin expression had significantly elevated risks of lymph node metastasis, distant metastasis, perineural invasion and an advanced American Joint Committee on Cancer (AJCC) stage compared with those with low vimentin expression and preserved E-cadherin expression, high vimentin expression and preserved E-cadherin expression, or low vimentin expression and loss of E-cadherin expression. Furthermore, multivariate analysis showed that high vimentin expression with loss of E-cadherin expression was an independent predictor of OS and DFS in patients with grade 1 and 2 pNETs who underwent resection (both P < 0.001). Conclusions The current study demonstrated that high vimentin expression with loss of E-cadherin expression was correlated with lymph node metastasis, distant metastasis, disease progression and a poor prognosis in patients with grade 1 and 2 pNETs who underwent resection.


Background
Pancreatic neuroendocrine tumors (pNETs) are a rare heterogeneous group of neoplasms that represent approximately 2% of all pancreatic neoplasms [1,2]. Advances in imaging technologies have improved the detection rate and diagnosis of this rare pancreatic disease [3]. pNETs can be subdivided into functional and nonfunctional cases. The majority of pNET cases (60-90%) are nonfunctional [4]. Compared with pancreatic ductal adenocarcinoma, pNETs have better long-term survival rates [5,6]. Recently, several large cohort studies found that lymph node involvement, tumor stage and grade, tumor size and Ki-67 index scores could predict the prognosis of pNETs [5][6][7]. However, some patients with small tumors or tumors with a low World Health Organization (WHO) grade (grade 1 or 2) may exhibit liver or lymph node metastasis and have a poor prognosis [8]. Little is known about the molecular and cellular mechanisms involved in the invasion and metastasis of pNETs.
Cancer cell invasion of surrounding normal tissues is a critical step in the invasion and metastasis of malignant disease [9]. Increasing evidence indicates that epithelialmesenchymal transition (EMT) plays critical roles in tumor development and metastasis [10][11][12]. In cancer progression and metastasis, cancer cells destroy or degrade the extracellular matrix, migrate and invade other tissues. Moreover, several EMT transcription factors, such as Snail, Slug, Twist, and Zeb, ultimately promote epithelial inhibition and mesenchymal feature induction [12]. Epithelial-cadherin (E-cadherin), a cell-surface adhesion molecule, is essential in maintaining apical-basal polarity in epithelial cells [13]. The expression of Ecadherin decreases during EMT in the processes of embryonic development, tissue repair and cancer metastasis. Vimentin, a hallmark of EMT, is involved in cellular motility, cell shape maintenance and directional migration [14]. It was reported that acquisition of vimentin expression and loss of E-cadherin expression during EMT results in tumor metastasis, invasion, radioresistance and generation of cancer cells with stem cell-like characteristics in pancreatic cancer [15].
With the aim of gaining insight into the molecular and clinical mechanisms underlying metastatic progression, the present study evaluated the expression of vimentin and E-cadherin and their effects on the progression and prognosis of patients with grade 1 and 2 pNETs who underwent surgery.

Study population
The medical data of patients with grade 1 and 2 pNETs undergoing surgical resection between January 2007 and November 2019 at the Second Affiliated Hospital and First Affiliated Hospital of Zhejiang University School of Medicine were retrospectively reviewed. A diagnosis of pNETs was made using standard histological criteria. The following clinicopathological data were collected for the patients: age; sex; symptoms at presentation; tumor location; type of surgical procedure; pathological characteristics including tumor size, lymph node involvement, perineural invasion and Ki-67 index; and stage. This study was approved by the Ethics Review Committee of the Second Affiliated Hospital of Zhejiang University School of Medicine.

Immunohistochemistry
Immunohistochemical staining was performed using a standard avidin-biotin-peroxidase complex procedure. Briefly, five-micrometer-thick sections were cut and subjected to antigen retrieval using citrate buffer (pH = 6.0). The sections were then incubated with primary antibodies (anti-vimentin (ab8978) at 1:200, anti-E-cadherin (ab1416) at 1:100, Abcam Inc., Cambridge, UK) overnight at 4°C, followed by incubation with a secondary antibody for 1 h at room temperature. The immunohistochemical reaction was visualized with 3,3 diaminobenzidine (DAB) as the substrate.
All tissue sections were simultaneously assessed by two investigators in a blinded manner. The immunohistochemical signal intensity was scored using the following scale: 0 for background staining, 1 for faint staining, 2 for moderate staining, and 3 for strong staining. In addition, the percentage of positive cells was graded according to the following scale: 0 for < 5%, 1 for 5-25%, 2 for 26-50%, 3 for 50-75%, and 4 for 75-100%. These two parameters were multiplied to produce a weighted score for each specimen; 0-2 and ≥ 3 were considered negative and positive staining, respectively.

Follow-up
Clinical follow-up was conducted by reviewing hospital medical records or via telephone. Patients were usually evaluated at our department every 6 months for the first 5 years after surgery and once a year thereafter. The postoperative follow-up data collected included clinical symptoms and signs, laboratory test results and imaging examination findings. Overall survival (OS) was defined as the time interval between the date of surgery and the date of death or last follow-up. Disease-free survival (DFS) was defined as the period from the date of surgery to the date of tumor recurrence or last follow-up.

Statistical analysis
Results are presented as the mean ± standard derivation (SD), and all statistical analyses were performed using SPSS 26.0 software (IBM Corp., Armonk, NY, USA). The associations between EMT markers (vimentin and E-cadherin) and other prognostic factors were analyzed using the chi-square test or Fisher's exact test. The Kaplan-Meier method and log-rank test were used to calculate and compare OS and DFS. Univariate and multivariate Cox regression models were performed to analyze prognostic factors. A P-value < 0.05 was considered statistically significant.

Patient characteristics
A total of 227 patients were included in the present analysis. These patients were diagnosed at a mean age of 52.48 ± 13.55 years and were evaluated over a mean follow-up period of 69.66 ± 35.49 months. Of the 227 patients with pNETs, 94 (41.4%) had their disease detected incidentally during physical examination. The most common symptom was abdominal pain (n = 64), which was frequently accompanied by hypoglycemia, abdominal discomfort and jaundice. The median size of pNETs was 2.5 (range, 0.4-19.0) cm. The most common tumor location in the pancreas was the head (n = 78, 47.1%), followed by the neck (n = 25, 36.6%) and then body and tail (n = 124, 16.3%). Among the patients, 222 underwent curative resection (R0 resection, 97.8%), while the others received palliative surgery (R1 resection, 2.2%). The surgical procedures included distal pancreatectomy (n = 108), pancreaticoduodenectomy (n = 72), enucleation (n = 30), middle pancreatectomy (n = 16), and total pancreatectomy (n = 1). Lymph node metastasis was confirmed pathologically in 24 (10.6%) patients. One hundred seventeen (51.5%) of the patients had grade 1 disease, and the remaining 110 (48.5%) had grade 2 disease. The majority of patients (193/227, 85.0%) had stage I or II disease.
At the time of the last follow-up, 34 patients had relapsed, and 16 patients had died. For the entire population, the 1-, 3-and 5-y OS rates were 99, 95 and 92%, respectively, and the 1-, 3-and 5-y DFS rates were 94, 86 and 85%, respectively.

Associations between vimentin/E-cadherin expression and other clinicopathologic parameters in pNETs
E-cadherin expression was identified in the membrane of pNET cells, while vimentin expression was identified in the cytoplasm of pNET cells (Fig. 1). Preserved E-cadherin expression was observed in 110 patients with pNETs (48.0%) (Fig. 1a), while loss of E-cadherin expression was observed in 117 patients with pNETs (Fig. 1b). In the 227 patients, high and low vimentin expression levels were observed in 55 (24.2%) and 172 (75.8%) patients, respectively ( Fig. 1d and e). Furthermore, vimentin expression was more frequently observed in tumors with lymph node (LN) metastasis (P < 0.001), distant metastasis (P = 0.002), a larger size (P = 0.044), perineural invasion (P = 0.023), a higher WHO grade (P = 0.010) or an advanced American Joint Committee on Cancer (AJCC) stage (P < 0.001) ( Table 1). Similar to the results for vimentin, loss of E-cadherin expression was more common in tumors with a higher T-stage (P = 0.026), LN metastasis (P = 0.015), distant metastasis (P = 0.022), a larger size (P = 0.003), perineural invasion (P = 0.007), a higher WHO grade (P < 0.001) or an advanced AJCC stage (P = 0.002) ( Table 1). No significant difference were observed in terms of sex, age, tumor location or symptoms with respect to the expression of vimentin or E-cadherin.
As acquisition of vimentin and loss of E-cadherin expression during EMT contribute to tumor invasiveness and metastatic capacity in cancer, we divided all patients into two groups as follows: the high vimentin and lost E-cadherin expression group (n = 42) and the 'other group' (patients with low vimentin and preserved E-cadherin expression, high vimentin and preserved E-cadherin expression, or low vimentin and lost E-cadherin expression) ( Table 2). Tumors with high vimentin and lost E-cadherin expression were more common in patients with LN metastasis (P < 0.001), distant metastasis (P = 0.003), perineural invasion (P = 0.034) and an advanced AJCC stage (P < 0.001). Additionally, 1/117 patients with G1 tumors exhibited distant metastasis at  Furthermore, the 1-, 3-and 5-year OS rates of the high vimentin and lost E-cadherin expression group were markedly lower than those of the other group (95.2, 77.7 and 67.2% vs 99.4, 98.9 and 98.2%, respectively, P < 0.001) (Fig. 2a), and the 1-, 3-and 5-year DFS rates of the high vimentin and lost E-cadherin expression group were also significantly lower than those of the other group (78.2, 49.4 and 49.4% vs 97.3, 94.3 and 93.5%, respectively, P < 0.001) (Fig. 2b). Therefore, our research showed that high vimentin expression with loss of E-cadherin expression during EMT was correlated with poor patient survival after resection of pNETs.
By multivariate analysis, high vimentin with lost Ecadherin expression and AJCC stage were found to be independent predictive factors for OS (both P < 0.05) ( Table 3), whereas high vimentin with lost E-cadherin expression, distant metastasis, AJCC stage and WHO classification were independent predictors for DFS (all P < 0.05) ( Table 4).

Discussion
In the current study, we showed that the analysis of vimentin and E-cadherin coexpression had prognostic importance in patients with grade 1 and 2 pNETs. pNETs in the high vimentin and lost E-cadherin expression group and the 'other group' were considered to have mesenchymal and epithelial phenotypes, respectively. We observed that pNETs with a mesenchymal phenotype frequently had LN metastasis, distant metastasis, perineural invasion and an advanced AJCC stage. Furthermore, high vimentin with lost E-cadherin expression was an independent predictive factor for OS and DFS in patients with grade 1 and 2 pNETs who underwent resection.
In recent years, increasing molecular data for pNETs have accumulated [16,17]. However, the genetic basis of pNET progression and metastasis remains unclear. EMT refers to a mechanism whereby tumor cells acquire the features of mesenchymal cells [18]. During EMT, cancer cells lose the ability to recognize specific targets and usually develop autocrine loops for growth factors, which play essential roles in providing self-sustaining growth signals to cancer cells [19]. E-cadherin, which is  [20][21][22]. Vimentin, a mesenchymal marker, can play fundamental roles in tumor invasion and metastasis. It has been reported that high vimentin and reduced E-cadherin expression is an important predictor in various types of cancers, such as gastric cancer, colorectal cancer and pancreatic cancer [23][24][25].
To date, a few studies have been conducted to evaluate the expression of EMT-specific transcription factors in neuroendocrine tumors [26][27][28]. Fendrich et al. immunohistochemically evaluated the expression of the EMT  [26], which was similar to the results of Yonemori K [29]. However, no statistically significant correlation was found between Snail/Twist expression or loss of E-cadherin expression and OS, but there was an inverse association between E-cadherin and Snail/Twist. Regarding pulmonary neuroendocrine tumors, Hwang W et al. showed that EMT could contribute to EGFRtyrosine kinase inhibitor (TKI) resistance [30]. In our study, we found that grade 1 and 2 pNETs with high This study has several potential limitations that must be considered. First, the study was retrospective in design and was subject to selection bias and diagnostic bias. Second, our sample may not be generally representative because all the patients included in this study were Chinese. Additionally, only patients with grade 1 and 2 pNETs undergoing surgical resection were included in the study, so this work does not cover most advanced cases; thus, our results may not apply to patients without indications for surgical resection due to an advanced stage. Despite these limitations, the present study is valuable because it identifies vimentin and E-cadherin as potential prognostic markers to predict the survival of patients with pNETs undergoing surgical resection.

Conclusions
The current study demonstrated that high vimentin and loss of E-cadherin expression were correlated with LN metastasis, distant metastasis, disease progression and a poor prognosis in patients with grade 1 and 2 pNETs who underwent resection.