E-cadherin is present in the epithelial cells and its aberrant expression is correlated with different kinds of head and neck squamocellular carcinomas. The purpose of the present study was to identify the expression particularities of analyzed E-cadherin in rapport with the localization and the differentiation of various head and neck squamocellular carcinomas. 18 biopsy fragments obtained by squamocellular carcinoma patients (larynx, pharynx, hard palate, tongue, submandibular, lip, gingival sulcus, nasal pyramid, maxillary, zygomatic) were processed by immunohistochemical staining. Immunoreactions for E-cadherin in the tumoral cells were examined according to the score: 0 (0% positive cells of specimen); 1 (<10% positive cells of specimen); 2 (10% - 30% of specimen); 3 (>30% of specimen). The immunohistochemical staining indicated the presence of 12 cases of well-differentiated squamocellular carcinoma (7 cases with score 3, 3 cases with score 2 and 1 case with score 1). Moderately-differentiated carcinomas were observed in the 3 cases (2 with score 2 and 1 with score 1). The poorly-differentiated histopathological type was present in 3 cases (all with score 1). Three types of E-cadherin distribution patterns were found: cytoplasmatic; cytoplasmatic and membranar; membranar. The presence of maximum score (value 3) of E-cadherin was found in well-differentiated squamocellular carcinomas of laryngeal, tongue, lip, nasal pyramid, and zygomatic area origin. A lower value of the score was present in the less differentiated histopathological type.
Cadherins, whose name derives from “calcium-dependent adhesion”, represent a class of type 1 of transmembranar proteins [
E-cadherin (ECAD) glycoprotein (codified by gene CDH1, situated on the 16q22.1 chromosome) has an important role in establishing and maintaining the intercellularly contacts and morphogenesis. The terminal cytoplasmatic end of ECAD molecule has proved to be linked to the actin of the cytoskeleton by means of α-catenin and β-catenin [
The head and neck squamocellular carcinomas (HNSCC) represent a frequent malignant condition with significant incidence and mortality [
The aberrant expression of E-cadherins was associated with the invasive character of neoplasms and the onset of metastasis in different types of carcinomas including those of the head and neck [
There are several mechanisms for the abnormal expression of ECAD in cancer, including the loss of CDH1 allelic locus, as well as somatic and more rarely, germline mutations. Regression of ECAD transcription by hypermethylation was also observed in several tumoral types and cell lines [
Despite progresses in the surgical treatment and radiotherapy of the latest years, the prognosis is still negative in the advanced cases [
The aim of the present study was to identify the particularities of E-cadherin expression analyzed in rapport with the localization in different head and neck regions [
Our study included a number of 18 biopsy fragments obtained by patients with squamocellular carcinoma—7 at the level of the larynx, 2 with pharyngeal origin, 1 from hard palate, 1 from tongue, 1 submandibular, 2 from the lip, 1 from gingival sulcus, 1 from nasal pyramid, 1 maxillary and 1 zygomatic.
All the patients approved the research and accorded with the publication of data.
The biopsy fragments were fixed in tamponated formalin 10% for 48 hours, then included in paraffin. Sections with 5 micrometers thickness were obtained by each case. Deparaffinization and rehydration of the sections was followed by exposure to heat, pH 6 solution for 30 minutes. The immunohistochemical staining was continued with a blockage of the endogeneous peroxidase by using oxygenated water 3%. Incubation with primary antibody E-cadherin (clone 36B5, ready to use, Novocastra, Newcastle upon Tyne, UK) was made for 15 minutes. As a technique, we used LSAB ± HRP applied for 30 minutes. The chromogene used was 3,3-diami- nobenzidine, and for counter-coloration we applied modified Lille hematoxylin. All the stages of the immunohistochemical staining were carried out with the help of the immunohistochemistry automaton (Dako Cytomation Autostainer). The microscopic examination was performed with microscope Nikon Eclipse E 600 and the images were obtained by using the LUCIA G system. Immunoreactions for ECAD in the tumoral cells were examined according to the following score: 0 (0% positive cells of specimen), 1 (<10% positive cells), 2 (10% - 30%), 3 (>30%).
The morphological staining indicated the presence of 12 cases of well-differentiated squamocellular carcinomas (5 laryngel cases, 2 pharyngeal, 2 from the lip, 1 from the tongue, 1 from the zygomatic area, 1 from the nasal pyramid). Moderately-differentiated carcinomas were observed in the 2 cases of larynx and in 1 case of hard palate. The poorly-differentiated histopathological type was present in cases derived by the region of the gingival sulcus, upper maxillary and submandibular areas (1 in each case).
The immunohistochemical reaction for E-cadherin was present in all the cases included in the study. The tumoral cells expressed E-cadherin in different percentages with values of the score ranging between 1 and 3. The intensity of the immunohistochemical reaction varied between 1—weak, 2—moderate and 3—intense, with two models of distribution-homogeneous and heterogeneous in the same tumoral region. 3 patterns of expression were observed: membranar, cytoplasmatic and membranar, cytoplasmatic (
For the squamocellular carcinomas localized in the laryngeal area, we noticed the following values of the score: score 3 (more than 30% positive tumoral cells for E-cadherine) in two cases, score 2 (10% - 30% tumoral cells expressed E-cadherin) in four cases and score 1 (less than 10% positive tumoral cells) in one of the cases.
In one of the cases with score 3, we observed a distribution in the whole tumoral area but the expression pattern was cytoplasmatic in the cells at the peripheral area, while in the center the cytoplasmatic and of membranar expression prevailed or the membranar one. The intensity of the immunohistochemical staining was maximum in the central cells of the tumoral area. The second case of laryngeal area quantified with score 3, presented both cytoplasmatic and membranar pattern but also only membranar, the latter one prevailing (
In two of the score 2 cases, we observed the variation of E-cadherin expression when crossing from the quasi-normal area to the hyperplasia area and then to the tumoral one. In the tumoral area, the E-cadherin expression in the surface epithelium decreases and increases in the tumoral region where it presents a membranar prevailing pattern, average intensity of reaction, and a homogeneous distribution pattern in the whole tumoral area (Figures 3(A)-(C)).
The other two cases with laryngeal origin with score 2, presented all three patterns of expression: cytoplas- matic, cytoplasmatic and membranar and membranar, but the membranar was prevailed. The intensity of the immunohistochemical staining was similar to the score.
In the laryngeal squamocellular carcinoma with score 1 the cytoplasmatic pattern prevailed, homogeneous distribution in the whole tumoral area and the intensity of the immunohistochemical reaction was similar to the score. In this case, we observed the presence of mitosis with high frequency (
The two cases of squamocellular carcinomas with pharyngeal origin belonging to the well-differentiated type, presented an E-cadherin expression in 10% - 30% of the tumoral cells, that is score 2. We observed different intensities of the immunohistochemical staining in different tumoral area while an homogeneous intensity in the same region. The values of the immunohistochemical staining were close to those of the percentage score 2 and 3. The distribution pattern was homogeneous with positive cells in the entire tumoral area. The expression pattern was cytoplasmatic, membranar, cytoplasmatic and membranar. In some cases we detected a prevailing cytoplasmatic pattern in the cells from the center of the tumoral region and intensity score 3 of the immuno- histochemical staining in these cells. In the second case cytoplasmatic and membranar pattern prevailed but the other patterns were also present (cytoplasmatic, membranar) in the tumoral region (
For the squamocellular carcinoma with tongue origin, well-differentiated as histopathological type, we observed a score 3 that indicates the percentage of tumoral cells which are positive to E-cadherin. We observed a homogeneous distribution in all the cells of the tumoral region with a cytoplasmatic and membranar prevailing expression pattern and higher intensity of the reaction in the cells situated in the center of the tumoral region (Figures 5(A)-(B)).
Both well-differentiated squamocellular carcinomas with lip origin presented a score 3 value. We also observed an intense immunohistochemical staining with membranar prevailing pattern in particular in the cells from the center of the tumoral areas (Figures 6(A)-(B)). Isolated, we also observed the presence of the cytoplasmatic and cytoplasmatic and membranar patterns.
In the case of the well-differentiated squamocellular carcinoma, localized in the zygomatic area, we noted a percentage of more than 30% of tumoral cells that are positive to E-cadherin, score 3. The distribution pattern was homogeneous in the entire tumoral area and from the three cytoplasmatic and cytoplasmatic and membranar patterns prevailed (
The squamocellular carcinoma localized in the area of the nasal pyramid presented score 3 of E-cadherin, distribution of the tumoral cells in the whole area, cytoplasmatic and membranar patterns of expression (
The squamocellular carcinoma localized at the level of the hard palate, belonged to the moderately- differentiated type, expressed E-cadherin in the tumoral cells in a percentage of 10% - 30% (score 2). The intensity of the immunohistochemical staining was similar to the score, the distribution was homogeneous both in the center as well as at the periphery of the tumoral regions. Considering the three patterns of expression, cytoplasmatic, membranar, cytoplasmatic and membranar, the membranar had the highest occurrence.
For the poorly-differentiated carcinomas as histopathological type, of the upper maxillary area, and of submandibular or gingival sulcus we observed score 1—less than 10% positive tumoral cells (
The studies carried out in different types of cancer researched the involvement of E-cadherin in the tumoral suppression. At an experimental level, the suppression of E-cadherin function or expression induce mesenchymal morphology and an increased cell migration and invasion as well as a tendency to metastasis. The tumoral suppressor role of E-cadherin was demonstrated or suggested in a variety of epithelial neoplasms: the hepatocellular carcinoma, the head and neck, skin, esophagus squamocellular carcinoma, the melanoma.
A study carried out by Rosado and colab. [
We have also noticed this aspect; all the 18 cases studied presented a score of the expression with values ranging between 1 and 3. About the expression patterns observed, the authors observed the cytoplasmatic
expression in just one of the cases, all the others having a cytoplasmatic and membranar pattern. We observed this latter pattern in most of the cases, but associated with isolated cells with cytoplasmatic or membranar expression (especially in the lip carcinomas).
A study performed by Wu and colabs. [
The role of E-cadherin in the squamocellular carcinomas is far from being clarified. It seems that the trials to estimate a prognosis in this clinical entity should include a combination between the molecular markers, the histopathological data and clinical parameters.