Correlation of NEDD4-1 and PTEN expression with the invasive capacity of pituitary adenomas

Abstract

The aim of the present study was to correlate the expression of neural precursor cell expressed developmentally downregulated 4–1 (NEDD4-1) and phosphatase and tensin homolog deleted on chromosome 10 (PTEN) with the invasive capacity of pituitary adenomas. A total of 50 pituitary adenoma tissues and 10 normal pituitary tissues were divided into the invasive group (26 cases), the non-invasive group (24 cases) and the normal group (10 cases). The expression of NEDD4-1 and PTEN was determined by immunohistochemistry. NEDD4-1 was revealed to be located in the nucleus and cytoplasm, whereas PTEN was only located in the cytoplasm. Furthermore, expression of NEDD4-1 was higher in pituitary adenomas compared with normal pituitary tissues (P<0.05), and higher in the invasive group compared with the non-invasive group, whereas the opposite trend was observed for PTEN. There was a strong negative correlation between NEDD4-1 and PTEN expression, indicating a dependency between the two and an association with invasiveness. In conclusion, NEDD4-1 may serve as a diagnostic and prognostic factor, and as a novel therapeutic target, in pituitary adenomas.

Introduction

Pituitary adenoma is a common type of neurological neoplasm and the third most common type of intracranial tumors. While pituitary adenomas are classified as benign tumors, a proportion of them exhibit invasive growth towards the surrounding normal structures, including the skull, cavernous sinus, dura, sphenoid bone, the third ventricle, and even the pharyngonasal cavity (1). Although recent studies have advanced the current knowledge on the pathogenesis of pituitary adenoma, the precise mechanisms and causes have remained elusive. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN), the first known tumor suppressor gene with phosphatase activity, was first cloned and named in 1997 (2,3). In 2007, neural precursor cell expressed developmentally down regulated 4-1 (NEDD4-1) was identified by Wang et al (4). NEDD4-1 has an important role in downregulating the levels of PTEN. It can promote the degradation of PTEN in the proteasome by adding a molecular marker, ubiquitin (4–8). To the best of our knowledge, no previous studies have assessed whether NEDD4-1 is expressed in pituitary adenomas or whether its expression is associated with their invasiveness or with PTEN. In the present study, the expression of NEDD4-1 and PTEN in invasive and non-invasive pituitary adenomas and normal pituitary tissues were analyzed using immunohistochemistry, and their correlation was assessed. The present study aimed to investigate the possible molecular mechanisms of the genesis and invasiveness of pituitary adenomas, and to identify biomarkers for early detection as well as characterization of the biological behavior of pituitary adenomas.

Materials and methods

Patients and reagents

The specimens for immunohistochemical analysis were collected from 50 patients with pituitary adenomas who underwent treatment at the Department of Neurosurgery of Heze Municipal Hospital (Heze, China) from July 2012 to May 2015. The patient cohort comprised 27 males and 23 females, with a male-to-female ratio of 1.17:1. The average age of the patients was 38.7 years (range, 18–78 years). According to the presence or absence of invasion of the tumors to the surrounding bones and cavernous sinus, patients were divided into the invasive group (26 cases) and the non-invasive group (24 cases) (Table I). Furthermore, 10 samples of normal pituitary tissues were obtained through normal autopsy. Rabbit anti-human NEDD4-1 polyclonal antibody (cat. no. bs-3506R-AF350; 1:200 dilution) and rabbit anti-human PTEN polyclonal antibody (cat. no. DM-0748R,1:300 dilution) were from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA), and secondary antibodies were from a designated immunohistochemistry kit for rabbit antibodies (Beijing Zhongshan Golden Bridge Biotechnology Co., Ltd., China). All experiments and use of the specimens in the present study were approved by the Ethics Committee of Heze Municipal Hospital (Heze, China), and all patients provided written informed consent prior to enrollment.

Table I.

Clinical data of patients with pituitary adenoma.

Characteristic	Invasive group (n)	Non-invasive group (n)
Cases	26	24
Age (years)
≥40	20	15
<40	6	9
Gender
Male	13	14
Female	13	10
Endocrine type
ACTH	2	5
GH	6	3
PRL	8	10
Others	10	6
Operative method
Transcranial	21	6
Trans-sphenoidal	5	18

ACTH, adrenocorticotropic hormone; GH, growth hormone; PRL, prolactin.

Immunohistochemical staining procedures

Paraffin-embedded specimens were cut into 4-µm thick sections, which were deparaffinized in turpentine, rehydrated in an ascending ethanol series and incubated in citrate buffer (0.01 mol/l, pH 6.0) with water bath heating (~98°C) for 15 min for antigen recovery. Following a general streptavidin-biotin complex immunohistochemical protocol (9), immunoreactivity was visualized with diaminobenzidine and the nuclei were counterstained with hematoxylin. Sections were then subsequently dehydrated in a series of graded alcohols, cleared in xylene and mounted. Prostate cancer samples were used as the positive control and slides incubated with phosphate-buffered saline without antibody were used as the negative control.

Evaluation of immunohistochemical staining

For each sample, 10 microscopic fields (magnification, ×200) were selected from the tissue sections with the strongest immune response. A total of 100 cells per field were counted and averaged. The percentage of positively stained cells was recorded. Staining was rated according to the color intensity and the percentage of positive cells. Positive staining was defined as the staining intensity being markedly higher than that of the background. Staining was classified into four categories according to the number of stained cells and the staining intensity: Negative [- (i.e., the staining intensity was not significantly different from the background)]; weakly positive [+ (i.e., the percentage of positively stained cells was <10%, or the staining intensity was weakly positive or only individual cells were positive to strongly positive)]; moderately positive [++ (i.e., the percentage of positive cells was 10–60%)]; strongly positive [+++ (i.e., the percentage of positively stained cells was >60%, or the staining intensity was moderately to strongly positive and only a few cells were weakly positive]. The known positive prostate section was selected as the positive control.

Statistical analysis

SPSS 18.0 software was used for statistical analysis. The two-samples t-test and analysis of variance were used to assess differences between groups. The χ² test and exact test on a four-fold table were used to determine differences in the positive staining rate between normal pituitary tissues and invasive, as well as non-invasive, pituitary adenomas. The Line × List χ² test and the one-sided test were used for correlation analyses. α=0.05 was considered as the level of significance. P<0.05 was considered to indicate a statistically significant difference.

Results

NEDD4-1 expression in pituitary tissues/adenoma increases with the degree of malignancy

Immunohistochemistry revealed that NEDD4-1 was expressed in the cytoplasm and/or the nucleus (Fig. 1). The positive rate of NEDD4-1 expression in the normal control group [10.0% (1/10)] was significantly lower compared with that in the experimental group [52.0% (26/50); P<0.05] (Table II). The positive rate of NEDD4-1 was 37.5% (9/24) in the non-invasive pituitary adenomas group and 65.3% (17/26) in the invasive adenomas group, thereby revealing a significantly increasing trend with the increasing degree of tumor invasiveness (P<0.05); the differences were also significant compared with the control group (P<0.05).

Figure 1.

NEDD4-1 expression in normal pituitary tissue and pituitary adenomas (magnification, ×200). NEDD4-1 was expressed in the cytoplasm and/or the nucleus. The expression of NEDD4-1 in (A) normal pituitary tissues was lower compared with that in (B) the non-invasive group (P<0.05), which was in turn lower compared with that in (C) the invasive group. NEDD4-1 expression therefore increased with the degree of tumor invasiveness. NEDD4-1, neural precursor cell expressed developmentally downregulated 4–1.

Table II.

Protein expression of neural precursor cell expressed developmentally downregulated 4–1 in normal pituitary tissues and in pituitary adenoma (invasive and non-invasive).

			Positive (n)
Group	Cases (n)	Negative (n)	+	++	+++	Total positives (n)	Positive rate (%)
Normal	10	9	1	0	0	1	10.0
Non-invasive	24	15	5	4	0	9	37.5a
Invasive	26	9	4	6	7	17	65.3b

^aP<0.05 compared with the normal group

^bP<0.05 compared with the non-invasive group.

PTEN protein expression in pituitary tissues/adenoma decreases with increasing degree of malignancy

Immunohistochemistry revealed that PTEN was mainly expressed in the cytoplasm, displaying as a brownish-yellow stain (Fig. 2). The rate of PTEN expression in the normal control group [100.0% (10/10)] was significantly higher compared with that in the experimental group [54.0% (27/50); P<0.05] (Table III). The positive rate of PTEN was 83.3% (20/24) in the non-invasive pituitary adenoma group and 26.9% (7/26) in the invasive pituitary adenoma group, thereby revealing a significantly decreasing trend with the increasing degree of tumor invasiveness (P<0.05); the differences were also significant compared with the control group (P<0.05).

Figure 2.

PTEN expression in normal pituitary tissue and pituitary adenomas (magnification, ×200). PTEN was mainly expressed in the cytoplasm, displaying as a brownish-yellow stain. The expression of PTEN in (A) normal pituitary tissues was higher compared with that in (B) the non-invasive group (P<0.05), which was in turn higher compared with that in (C) the invasive group. The positive rate had a significantly decreasing trend with the increasing degree of tumor invasiveness. PTEN, phosphatase and tensin homolog deleted on chromosome 10.

Table III.

Protein expression of phosphatase and tensin homolog deleted on chromosome 10 in normal pituitary tissues and in pituitary adenoma (invasive and non-invasive).

			Positive (n)
Group	Cases (n)	Negative (n)	+	++	+++	Total positives (n)	Positive rate (%)
Normal	10	0	2	3	5	10	100.0
Non-invasive	24	4	5	5	10	20	83.3a
Invasive	26	19	4	2	1	7	26.9b

^aP<0.05 compared with the normal group

^bP<0.05 compared with the non-invasive group.

Inverse correlation of NEDD4-1 and PTEN protein expression in pituitary adenomas

Among the 26 cases of pituitary adenomas which stained positive for NEDD4-1, four were positive for PTEN. Furthermore, among the 27 cases of pituitary adenomas which stained positive for PTEN, 24 were negative for NEDD4-1. Statistical analysis revealed a negative correlation between the two proteins (γ=−0.711, P<0.05) (Table IV).

Table IV.

Correlation of NEDD4-1 and PTEN expression in pituitary adenomas.

	PTEN
NEDD4-1	Positive (n)	Negative (n)	Total (n)
Positive	4	22	26
Negative	23	1	24
Total	27	23	50

χ²=30.347; P<0.05; correlation coefficient γ=−0.711; α=0.05. NEDD4-1, neural precursor cell expressed developmentally downregulated 4–1; PTEN, phosphatase and tensin homolog deleted on chromosome 10.

Discussion

In general, the growth of pituitary adenomas is limited; however, in certain cases, they may invade the surrounding brain tissues, blood vessels and nerves, and destroy the sellar bone, thereby showing characteristics of malignant tumors that require complete surgical resection (10–12). According to the concepts of modern molecular biology of tumors, the occurrence and development of tumors constitutes a multi-factorial, multi-step and complex biological evolutionary process involving the mutation of multiple genes, and pituitary adenoma is no exception (13–15). PTEN is among the tumor suppressor genes with the highest vulnerability to mutations (16,17). NEDD4-1 is a newly discovered ubiquitin ligase of PTEN, with HECT (homologous to the E6-AP carboxyl terminus) domains. NEDD4-1 has a role in the multi-ubiquitination of PTEN and degradation of its proteasome (4,18,19). In the present study, the expression of PTEN and NEDD4-1 in invasive and non-invasive pituitary adenomas and normal pituitary tissues was explored using immunohistochemistry and their correlation was analyzed.

Although the genetic status of PTEN was not evaluated in the present study, it is likely that inactivation of PTEN may have led to the loss of protein expression detected by immunohistochemistry. Of note, the loss of PTEN protein expression is an important negative prognostic indicator (20–22). Immunohistochemical analysis may be the best method for evaluating the PTEN status, as it is able to detect PTEN loss due to various causes, including the inactivation of the gene product (23–25). By using immunohistochemistry, the present study revealed that the rate of PTEN-positive cells was significantly different between patients with non-invasive pituitary adenomas [83.3% (20/24)] and those with invasive pituitary adenomas [26.9% (7/26); P<0.05], whereas 100% of cells in normal pituitary tissues were PTEN-positive. This result indicated that the expression intensity of PTEN was reduced with the increase in the degree of tumor invasiveness. It can be speculated that deletion of the PTEN gene is one of the reasons of decreased protein levels in pituitary adenomas compared with normal pituitary tissues.

The positive rate of NEDD4-1 expression in normal pituitary tissues was 10.0%, which was significantly lower compared with that in pituitary adenomas (52.0%; P<0.05). Furthermore, the NEDD4-1-positive rate in the non-invasive pituitary adenoma group (37.5%) was significantly lower compared with that in the invasive group (65.3%; P<0.05), indicating that NEDD4-1 may be associated with the degree of malignancy or loss of histological differentiation. It was speculated that, with an increasing degree of malignancy, NEDD4-1 protein participated in PTEN protein degradation by polyubiquitylation, thus resulting in increased NEDD4-1 protein expression. Therefore, the overexpression of NEDD4-1 is likely to have an important role in the development of pituitary adenoma.

To the best of our knowledge, the present study was the first to assess NEDD4-1 and PTEN expression in pituitary adenoma. Among 26 cases of NEDD4-1-positive pituitary adenoma, four were PTEN-positive, whereas, among 27 cases of PTEN-positive pituitary adenoma, 24 were NEDD4-1-negative. Statistical analysis revealed a negative correlation between NEDD4-1 and PTEN (γ=−0.711; P<0.05). With the increasing degree of invasiveness of pituitary adenoma, the NEDD4-1-positive rate was increased, whereas the PTEN-positive rate was decreased. A possible underlying mechanism is that increased expression of NEDD4-1 leads to an increase in PTEN ubiquitination, thus causing its degradation in the proteasome.

In conclusion, the present study showed that NEDD4-1 and PTEN may have an important role in the occurrence and development of pituitary adenoma, which was associated with the degree of invasiveness and prognosis of pituitary adenoma. The two proteins may thus be utilized as diagnostic and prognostic biomarkers, as well as indicators for determining the biological characteristics of pituitary adenoma. However, the specific mechanisms of the roles of NEDD4-1 and PTEN in pituitary adenomas remain to be fully elucidated by further experimental studies.