MATERIALS AND METHODS

Patients

This prospective study involved women with EA who were treated in 2015 in the Grodno and Gomel regions in the Republic of Belarus. The inclusion criteria for the study were a presence of stage I-III EA (International Federation of Gynecology and Obstetrics [FIGO], 2009), hysterectomy and an absence of malignant tumors in other locations during life. EA stage IV (FIGO, 2009), Lynch syndrome, palliative treatment, a presence of synchronous and metachronous malignancies and the presence of other specific growth patterns of EA were the exclusion criteria for this study [11].

The presence of the MELF pattern was confirmed independently by three pathologists (D.A.Z., S.L.A., and M.G.Z.). The pattern was identified by the presence of elongated, dilated (microcystic) and disrupted invasive tumor glands with peri-glandular fibromyxoid stromal reactions and single invasive tumor cells in the stroma around the pattern (Fig. 1).

A total of 100 out of 424 cases of EA during the study period were determined to be eligible for inclusion in this study. Patients were divided into two groups according to the presence or absence of MELF pattern. The first group included 49 subjects who had EA with stroma-specific MELF pattern (MELF positive group). The second group consisted of 51 patients who had no MELF pattern changes in the stroma (MELF negative group). The observation period was 36 months. All patients received treatment according to the National Protocols of Diagnostics and Treatment of Oncological Diseases of the Republic of Belarus. Clinicopathological characteristics of patients are presented in Table 1.

Immunohistochemistry

The primary antibodies used in this study were ready-to-use monoclonal mouse Gal-1 (Abcam, Cambridge, UK), anti-VEGF (Diagnostic Biosystems, Pleasanton, CA, USA), and anti-CD34 (Diagnostic Biosystems). An UnoVue HRP/DAB Detection System (Diagnostic Biosystems) was used for primary antibody visualization.

The method employed in this study has been described in our previous work [10,11]. Briefly, sections of tissue (4 to 5 µm thick) were deparaffinized and washed with distilled water. Antigen retrieval was performed using a microwave. The sections were then allowed to cool and endogenous peroxidase blocking was performed in 5% hydrogen peroxide. Blocking of nonspecific antibody binding was carried out in 5% casein. Sections were washed and incubated in a moist chamber at room temperature with corresponding primary antibodies followed by incubation with anti-mouse horseradish peroxidase secondary antibodies. The reaction product was visualized after 3,3-diaminobenzidine (DAB) staining for 5 minutes followed by Mayer’s hematoxylin counterstaining [10,11].

Morphometry

The morphometrical analysis was carried out using package NIS-Elements. The tumor invasion zone was photographed using a microscope (Nikon Eclipse 50i, Nikon, Tokyo, Japan) with a digital camera (DS-Fi2) in 5 non-overlapping high-power fields (HPF; ×400 magnification) of maximum expression for each marker. Expression of VEGF and galectin-1 in cell counting was analyzed using the function “measure.” The number of positive cells was expressed as a percentage of the total number of cells in the epithelial component of the tumor.

MVD was presented as the area and number of vessels per mm². The number of vessels was counted in 5 non-overlapping HPF in areas of “hot spots” and inverted into mm² using the formula:

N=Xn×1000000/118947.07

where N=number of vessels per mm²; Xn =mean number of vessels; and 118947,07=area of one HPF (µm²).

The area of the vessels was counted in 5 non-overlapping HPFs in regions of “hot spots” using the function “area.” Area of vessels after the count was inverted into mm² using the formula:

S=X s×1000000/118947.07

where S=area of vessels per 1 mm²; X s =mean area of vessels; and 118947,07=area of one HPF (µm²).

Statistical analysis

Power analysis (power=80%, α=0.05) during the pilot study, in which parameters were received from four cases with MELF pattern and four without the pattern in 5 HPF, revealed that the minimum number of subjects should be 18. The data were presented as the median, lower and upper quartiles. The Mann-Whitney test was used for comparing the study groups based on the evaluated criteria. The Spearman correlation test with Chaddock scale was used to perform correlation analysis. The hazard ratio (HR) with a 95% confidence interval (95% CI) was determined for overall survival (OS) and disease-free survival (DFS) using univariate and multivariate Cox proportional hazards regression models. A p<0.05 was considered statistically significant. GraphPad Prism v.7.29 (GraphPad Software Inc., San Diego, CA, USA) and R Software v 3.4.0 were used for analysis (R Foundation for Statistical Computing, Vienna, Austria).

Ethics statement

Immunohistochemical study was undertaken at the Gomel State Medical University, Belarus, with informed consent from all patients and with ethical approval from the Institutional Review Board (Gomel State Medical University), Gomel, Belarus.

RESULTS

Galectin-1 expression in EA tissue

Galectin-1 was observed to be diffusely expressed by epithelial cancer cells, stromal cancer cells and vessels in both groups. However, the intensity of the expression of this marker in the MELF negative group was significantly lower (p<.001) than the MELF-positive group (Fig. 2A, B). The median galectin-1 expression in the MELF pattern-positive and -negative groups were 78.6 % (40.1%–88.3%) and 34.2% (24.4%–55.5%), respectively. The Mann-Whitney test showed statistically significant differences in galectin-1 expression in both groups (p<.001).

VEGF

The expression of VEGF was also observed across all cancer cells and stromal elements. In the MELF-negative group, predominantly moderate expression of this marker was observed (Fig. 2C). In the MELF pattern positive group, the expression was substantially intense (Fig. 2D). Median VEGF expression in the MELF-positive group was 81.4% (58.1%–86.3%) and in the group without MELF pattern was 53.0% (47.6%–75.4%). The VEGF expression difference between the two groups was statistically significant (p<.001).

Microvessel density

In various regions of the MELF pattern, a low number of vessels was observed. In the group without MELF pattern, vessels were situated in small groups, and lymphovascular invasion of EA was mostly absent (Fig. 2E). A significant number of microvessels was seen in the MELF pattern cases in “hot spots” regions with unusual lumens. This was often observed in areas of lymphovascular invasion (Fig. 2F).

We also measured the number of vessels per mm² in these tissue sections. We found that the median values in MELF-negative and MELF-positive groups were 101.6 vessels/mm² (range, 90.1 to 127.9 vessels/mm²) and 134.5 vessels/mm² (range, 98.5 to 156.7 vessels/mm²), respectively, where the latter group showed significantly higher presence than the former (p<.010).

The area of vessels per mm² was also significantly higher (p< 0.001) in the stomal changes of the MELF-positive group (4,788.3 µm² /mm²; range, 3,087.3 to 5,130.4 µm² /mm²) compared to the group without such specific stromal changes (3,037.3 µm² /mm²; range, 2,508.3 to 5,130.4 µm² /mm²).

Correlation analyses

We also analyzed the associations among expressions of the MELF pattern, galectin-1, VEGF, area and number of vessels per mm², the outcome of EA (survival or death), and the number of days of survival (Fig. 3). For instance, galectin-1 demonstrated a moderate positive correlation with the area of vessels per mm² (p<.001, r=0.69) and VEGF expression (p<.001, r= 0.67). Furthermore, galectin-1 expression had a highly positive correlation with the outcome of EA (p<.001, r=0.78) and a highly negative one with the number of days of survival (p<.001, r=–0.84).

The expression of VEGF had a highly positive correlation with the outcome of EA (p<.001, r=0.85) and a highly negative correlation with the number of days of survival (p<.001, r=–0.78). The number of vessels per mm² revealed moderately positive correlations with galectin-1 (p<.001, r=0.54), area of vessels per mm² (p<.001, r=0.61), and VEGF (p<.001, r=0.56); a highly positive correlation with the outcome of EA (p<.001, r=0.71); and a moderately negative correlation with the number of days of survival (p<.001, r=–0.59).

A highly positive correlation was observed between the area of vessels per mm² and the outcome of EA (p<.001, r=0.73) and VEGF expression (p<.001, r=0.72). A highly negative correlation was found between the area of vessels per mm² and the number of days of survival (p<.001, r=–0.71).

MELF pattern had a slightly negative correlation with the number of days of survival (p<.001, r=–0.47) and slightly positive correlation with galectin-1 expression (p<.001, r=0.39), the area of vessels per mm² (p<.001, r=0.36), the outcome of EA (p<.001, r=0.42), and VEGF expression (p<.001, r=0.39).

Survival analysis

An OS univariate survival analysis was performed, indicating that all parameters except age play a role in the survival of patients with EA (Table 2). However, a multivariate Cox proportional hazard regression analysis of OS revealed that only the area of vessels per mm² (HR, 1.018; 95% CI, 1.002 to 1.033), galectin-1 (HR, 1.049; 95% CI, 1.025 to 1.074) and VEGF (HR, 1.049; 95% CI, 1.022 to 1.077) play key roles in survival irrespective of MELF pattern (Table 2).

A univariate analysis was performed, revealing that all parameters except age and tumor grade play a role in DFS of patients with EA (Table 3). However, our multivariate Cox proportional hazard regression analysis demonstrated that only MELF pattern (HR, 1.018; 95% CI, 1.002 to 1.033) and galectin-1 expression (HR, 1.049; 95% CI, 1.025 to 1.074) were significant predictors of DFS (Table 3).

DISCUSSION

In this study, we investigated the associations between galectin-1, VEGF, MVD, area of vessels, and survival outcome of EA patients with and without a MELF pattern. We identified 49 patients out of 100 with a MELF pattern and 51 patients without this stromal change who were observed throughout 36 months from admission to the hospital. In this immunohistochemical study, we demonstrated differential expressions of galectin-1, VEGF and measurement of MVD in cases with and without MELF pattern.

In the last two decades, several galectin family members have emerged as versatile modulators of tumor progression. Galectin-1 expression is also frequently reported to be increased in the reproductive system as well as the placenta. There is ample evidence that malignant transformation is accompanied by elevated galectin-1 levels [12]. Jeschke et al. [13] reported a statistically significant increase of galectin-1 expression in EA with grade 3 and stages III/VI (FIGO) compared to grades 1 and 2 and FIGO I/II. However, no data are available on the expression of galectin-1 in EA with different types of stromal changes and survival. In our study, we found that galectin-1 expression is higher in EA with a MELF pattern compared to cases without a MELF pattern. Our observation of positive correlations between galectin-1 expression and MELF pattern (fibromyxoid changes) and EA outcome agrees with our previous report and with a report by Sandberg et al. [14], in which a correlation was shown between an increased galectin-1 expression and fibrotic reaction in tumor progression in the stroma in colon cancer. This was accompanied by decreased immune cell infiltration, indicating a pro-cancerous role of galectin-1 [14,15].

VEGF was originally identified as a multifunctional cytokine in angiogenesis and lymphangiogenesis [16]. In cancer angiogenesis, VEGF promotes the mobilization of inflammatory cells to the tumor site, maintaining the local inflammatory process and inducing the synthesis of proangiogenic factors by endothelial cells, platelets, smooth muscle cells, inflammatory cells, fibroblasts, and tumor cells [17]. This interaction between tumor and stromal cells may result in an increased VEGF expression with cancer-associated fibroblasts being the primary source of VEGF [18]. Immature cells of the tumor microenvironment have higher secretion of VEGF than mature cells [19]. We suggest that this is the reason that in our study, MELF pattern stroma had higher expression of VEGF than normal stroma in EA.

Angiogenesis is also known to play crucial roles in the malignant behavior of tumors by increasing oxygen and nutrient supply to cancer cells where the neo-vasculatures form an irregular network of capillaries. In addition, such abnormal vasculatures are important as a pathway for cancer cell metastasis [20]. Accumulated evidence indicates that tumor angiogenesis assessed by blood MVD is associated with advanced clinicopathological parameters and poor prognostic outcomes in different types of cancers [21]. MVD analysis demonstrates high prognostic value in cancers of different locations, such as renal, cervical, colorectal and others [22,23]. In MELF pattern positive EA, an increased number and area of vessels were observed, which agrees with the previously reported study by Joehlin-Price et al. [24] on the high frequency of lymph node metastasis.

A moderate correlation between the area of vessels per mm² and galectin-1 may be due to the cross-talk between galectin– glycan interactions and vascular compartments [25]. The correlation between galectin-1 and VEGF may be associated with the mirroring effects of these proangiogenic factors [26]. Galectin-1 expression in EA may be a prognostic factor in OS of patients, an observation that was reported by Wu et al. [27]. That study reported predictive values of this parameter for cholangiocarcinoma, hepatocellular carcinoma, gingival squamous cell carcinoma, head and neck squamous cell carcinoma, renal cell carcinoma, nonsmall cell lung cancer, gastric carcinoma and glioblastoma multiforme [27].

VEGF as the main proangiogenic factor and immune suppressive factor of the tumor microenvironment correlates with the survival of patients suffering from EA. Goel and Mercurio [28] reported a strong expression of VEGF in endothelial cells in the stromal microvessels adjacent to malignant glands, which has been reported to be significantly associated with tumor progression and metastasis.

A positive correlation between MVD and galectin-1/VEGF expression suggested that these parameters play a role in angiogenesis. Additionally, a highly positive correlation between galectin-1 expression and poor survival, as well as MVD and poor survival, suggested that these factors may have a considerable predictive role in survival [29].

The presence of a MELF pattern revealed low correlations with the above parameters of proangiogenic response in EA. However, a low negative correlation of MELF pattern with the number of days of survival and a moderate positive correlation with the outcome of the disease may show that MELF pattern may be an independent prognostic criterion of patients’ OS.

The results of multivariate survival analyses showed that MELF pattern plays a role in DFS of patients with EA, but not in OS. However, our univariate analysis demonstrated a significant effect of MELF pattern on both OS and DFS. Previous reports have been contradictory on the role of MELF pattern. Sanci et al. [6] and our previous work reported a positive association, but other authors showed that the presence of a MELF pattern plays no role in OS. Our study also demonstrated MELF pattern as a predictive factor of DFS that may be associated with more frequent lymph node involvement in cases of MELF pattern presence. The absence of influence of FIGO and tumor grade on DFS and OS in our study could be associated with homogeneity of the comparison groups for these parameters. However, our inclusion and exclusion criteria eliminated any potential bias. The systematic review of Prodromidou et al. [30] revealed that most of the published literature describing the role of MELF patterns in patients’ survival did not study large cohorts of patients, which may be a factor in the inconclusive observations.

Potential limitations of this study are its case-control nature with a relatively small volume of cases due to the rare incidence of MELF patterns in EA. Despite these limitations, a number of study population characteristics mitigated the weaknesses and increased the validity of our results. One characteristic was the availability of excellent follow-up data. Another was that histopathological analyses made by experienced pathologists. Others included that uniform surgical and radiological treatment was provided by the same surgical teams in two oncological dispensaries and followed protocols of diagnostics and treatment of oncological diseases of the Republic of Belarus.

In conclusion, this study presented an increase of MVD in areas of “hot spots” and angiogenic factors such as VEGF and galectin-1 in cases of EA with MELF presence. Hence, these biomarkers may be used as potential targets for therapy of EA, especially in the implementation of personalized medicine in cases with such specific stromal changes. Our univariate survival analysis revealed MELF pattern presence to be an independent predictor in overall EA survival, but the multivariate analysis did not show that its combination with previously described parameters plays a role in survival. Thus, a large case-control study should be conducted to confirm our findings.

Fig. 1.

Specific microcystic, elongated and fragmented pattern changes: endometrioid carcinoma showing eosinophilic glands with microcystic transformation embedded in fibromyxoid stroma and cancer cell complexes with some areas resembling vascular invasion.

Fig. 2.

(A) A few positive glandular cells (microcystic, elongated and fragmented [MELF]–negative group). (B) All glandular cells positive for galectin-1 expression (MELF-positive group) in endometrioid carcinoma. (C) Positive local areas of cytoplasmic expression of vascular endothelial growth factor (VEGF; MELF-negative group). (D) Intense glandular and cytoplasmic (MELF-positive group) expression of VEGF in glands of the endometrioid carcinoma. Low (normal stroma) (E) and increased number of vessels (F) in fibromyxoid stroma situated around cancer cells forming gland without lumens.

Fig. 3.

A correlation plot. Days, number of days of survival from surgical treatment to death or end of observation; MELF, microcystic, elongated and fragmented pattern; NoV, number of vessels per mm² ; Gal-1, galectin-1 expression; AoV, area of vessels per mm² ; Surv, survival (survival or death); VEGF, vascular endothelial growth factor expression.

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Figure & Data

References

Citations

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