Ornithine decarboxylase and glutamate decarboxylase 65 as prognostic markers of gallbladder malignancy: A clinicopathological study in benign and malignant lesions of the gallbladder
- Xiaofeng Deng
- Dongni Pei
- Corresponding author:
- Dongni Pei [ firstname.lastname@example.org ]
Published online on: Monday, November 12, 2012
- Pages: 413-418 DOI: 10.3892/mmr.2012.1178
Gallbladder cancers are associated with a dismal prognosis, with a 5-year survival rate of <5% for those patients whose disease is not amenable to surgery (1). The majority of gallbladder cancers are adenocarcinomas, with a small percentage being squamous cell carcinomas. Chronic cholecystitis and cholelithiasis are risk factors for primary carcinoma of the gallbladder (2). In certain parts of the world, the incidence is comparatively high and contributes to a social disaster as a result of its poor outcome.
The surgical management of gallbladder cancer has always been controversial. Surgeons wordwide have repeatedly stressed the need for complete surgical resection. However, even among patients who undergo radical surgical resection, the reported median survival across all stages is 35–38% (3). An improved understanding of the clinicopathological features of gallbladder carcinogenesis may provide useful insights in the development of methods for the diagnosis and treatment of this deadly disease.
Ornithine decarboxylase (ODC) is the first and rate-limiting enzyme in polyamine biosynthesis. Polyamines are known to play key roles in cell proliferation and other biological processes. Polyamine biosynthesis is closely associated with physiological cell growth, proliferation, regeneration and pathological proliferation. It is necessary for cells to progress into the S phase; polyamine depletion arrests cells in G1. Elevated levels of ODC have been identified in gastric cancer, glioma, breast cancer, colon cancer, pancreatic cancer, lung cancer and prostate cancer, and may contribute to their carcinogenesis (4–8). γ-aminobutyric acid (GABA) is synthesized by glutamate decarboxylase (GAD), which has two forms, GAD65 and GAD67. The former may be related to the carcinogenesis, progression and biological behaviors of a number of malignancies. Several previous studies have suggested a connection between the GABAergic system and neoplastic processes (9,10). It has been confirmed that GABA content and GAD activity are increased in the neoplastic tissues in colon and breast cancer (11–13). In the current study, we observed the expression of ODC and GAD65 in gallbladder specimens by means of immunohistochemical analysis and analyzed the correlation between the expression levels of ODC and GAD65 and the clinicopathological features of the gallbladder lesions.
Materials and methods
A total of 108 gallbladder carcinoma specimens were collected from Xiangya Hospital, The Second Xiangya Hospital of Central South University and The People’s Hospital of Hunan Province, Changsha, China. Of these, 77 specimens came from female patients and 31 from males. All specimens were diagnosed as adenocarcinomas, of which 9 had adenoma lesions, 29 were highly differentiated, 29 moderately differentiated, 30 poorly differentiated and the remaining 11 were mucous adenomas. Surgery revealed the invasion of pericholecystic tissues and organs in 59 cases, local lymph node metastases in 59 cases and gallstones/cholelithiasis in 58 cases. Radical resection was applied to 34 cases and palliative resection/surgery to 48 cases while 26 cases were unresectable to surgery due to local invasion into critical structures or metastasis beyond regional confines. Data concerned with survival analysis were acquired for 67 cases by long-term follow-up of all patients, and the postoperative survival time was grouped as ≥1 year (20 cases) and <1 year (47 cases). From the 108 gallbladder adenocarcinoma samples, we obtained 46 sections of peritumoral tissues (distance to adenocarcinomas ≥3 mm), of which 10 were normal by pathological analysis and 10, 12 and 14 had mild, moderate and severe atypical proliferation, respectively. A total of 15 specimens of gallbladder diagnosed as adenomatous polyps were obtained from The Second Xiangya Hospital of Central South University, including specimens from 10 females and 5 males of average age 51.8±11.6 years (range 42–60 years). The adenomatous polyps were 8–15 mm in size, and 5 of the 15 had moderate to severe proliferation. In addition, 35 chronic cholecystitis specimens were obtained as controls, of which 15 were from patients with chronic cholecystitis alone and 20 were from patients with chronic cholecystitis and gallstones. Histologically, the 35 specimens included 11 with normal gallbladder mucosa, 12 with mild atypical proliferation, 7 with moderate atypical proliferation and 5 with severe atypical proliferation. All samples were fixed in 4% formaldehyde and 4-μm sections were prepared for immunohistochemical studies. The study was approved by the ethics committee of Second Xiangya Hospital, Central South University, Changsha, China. Written informed patient consent was obtained from the patient’s family.
For ODC and GAD65 detection, immunochemical staining was carried out using EnVision™ (ChemMate™ EnVision +/HRP/DAB, rabbit/mouse two step staining method) according to the instructions of the manufacturer (Dako Laboratories, Inc., Santa Barbara, CA, USA). Briefly, paraffin-embedded gallbladder adenocarcinoma tissues were cut into 4-μm-thick sections. The sections were deparaffinized and incubated with 3% H2O2 solution for 15 min, followed by EDTA-trypsinase digestion (0.125%, pH 9.0) for 15 min, then soaked with PBS (pH 7.4) 3 times, each for 5 min. The pre-treated sections were then incubated with rabbit anti-human ODC or GDA65 (Dako Laboratories Inc.) for 60 min at room temperature. Solution A (ChemMate EnVision +/HRP) was added and incubation was continued for another 30 min. Substrate DAB liquid was added and the sections were then hematoxylin counter-stained. The slides were dehydrated with different concentrations of alcohol and soaked in xylene for 5 min (3 times), and then mounted permanently with neutral balsam. The slides were examined independently by two pathologists. The results of ODC or GAD65 immunochemical staining were considered to be positive when >25% of the tumor cells were stained. The positive controls were provided by Bosite Inc. (Wuhan, China) and the negative controls used 0.01 mol/l PBS (pH 7.4) solution (to substitute for the first antibody).
The SPSS 19.0 software was used for calculation of the correlations between the ODC or GAD65 levels and the histological or clinical factors by the χ2 independence test. Fisher’s exact probability test was also used for analyzing statistical associations between two independent sample groups. P<0.05 was considered to indicate a statistically significant result. Disease-specific overall survival analyses were determined and compared using the Kaplan-Meier method and the log-rank test. For multivariate analysis, the Cox regression method was employed. 95% confidence intervals (CIs) were used.
Expression of ODC and GAD65 in human gallbladder adenocarcinoma, peritumoral tissues, adenomatous polyps and chronic cholecystitis
The number of cases staining positive for ODC and GAD65 were 65 and 59, respectively, among the 108 patients with gallbladder adenocarcinoma, 13 and 14, respectively, among the 46 peritumoral tissues, 3 and 4, respectively, among the 15 patients with adenomatous polyps and 4 and 6, respectively, among the 35 patients with chronic cholecystitis (Figs. 1–4). The number of positive stainings of ODC and GAD65 in the gallbladder adenocarcinoma tissues were significantly higher than those in the peritumoral tissues (P<0.01), adenomatous polyps (P<0.01 for ODC; P<0.05 for GAD65) and chronic cholecystitis (P<0.01). Moreover, mild, moderate or severe atypical proliferation was observed in all cases expressing ODC or GAD65.
Positive expression of ornithine decarboxylase (ODC) in moderately differentiated adenocarcinoma. EnVison™ immunohistochemistry, ×200.
Positive expression of glutamate decarboxylase 65 (GAD65) in peritumoral tissue with moderately atypical hyperplasia. EnVison™ immunohistochemistry, ×200.
Correlation of ODC and GAD65 expression with clinical and pathological features of gallbladder adenocarcinoma
The expression levels of ODC and GAD65 in cases with adenoma canceration or well-differentiated carcinoma or without lymph node metastasis or surrounding invasion were significantly lower than those in cases with poorly differentiated carcinoma, lymph node metastasis or surrounding invasion. No significant correlation was observed between the expression levels of ODC and GAD65 and the clinicopathological features of patients with gallbladder adenocarcinoma, including gender, age, tumor size and gallstones (Table I).
Correlation between disease-specific overall survival and expression of ODC and GAD65
Following surgical resection, only 67 of the 108 patients were successfully followed up via telephone or mail surveys, among which 20 cases had survived ≥1 year and 47 cases had succumbed to the disease <1 year postoperatively, with a mean survival time of 9.7±4.4 months. Of the 67 surviving patients, 40 had positive immunohistochemical staining of ODC and 36 had positive staining of GAD65. The relevance of the patients’ survival to the positive expression of ODC and GAD65 was examined by univariate Kaplan-Meier survival analysis. Overall survival was inversely associated with positive or increased expression of ODC (Fig. 5; P=0.009) and GAD65 (Fig. 6; P=0.006). The relevance of overall survival to other clinicopathological characteristics was also assessed by univariate analysis, which revealed that the overall survival was associated with tumor pathological type (P<0.01), tumor diameter (P<0.01), lymph node metastasis (P<0.01) and surrounding tissue invasion (P<0.01). All factors that showed significant association in the univariate Kaplan-Meier analysis were subsequently subjected to multivariate Cox regression survival analysis, which indicated that tumor maximum diameter ≥2 cm, lymph node metastasis and surrounding tissue invasion followed by ODC or GAD65 positive expression were the most significant predictors of short overall survival (Table II).
Univariate Kaplan-Meier survival analysis showed that overall survival was inversely associated with increased expression of ornithine decarboxylase (ODC), as illustrated by the dotted line (P=0.009).
Univariate Kaplan-Meier survival analysis showed that overall survival was inversely associated with increased expression of glutamate decarboxylase 65 (GAD65) as illustrated by the dotted line (P=0.006).
Multivariate Cox regression analysis of overall survival in 67 patients with surgical resection of gallbladder carcinoma.
ODC, a key enzyme in polyamine metabolism, is observed in numerous types of cells from humans and animals. It is a dimer consisting of two 50-kDa subunits. The ODC-related sequences, including ODC1 and ODC2, are present on human chromosomes 2p25 and 7q31 respectively. ODC1 is an important functional gene which exists universally in organisms, whereas ODC2 is a pseudogene which exists only in the human body and is without a clear function. The degradation of ODC depends mainly on ODC antizyme (OAZ) which functions not by suppressing the synthesis of ODC but by formulation of an ODC-antizyme complex. The latter is generated to promote the degradation of ODC by the 26S proteasome and polyamine synthesis is subsequently decreased. Polyamines have been shown to be closely associated with cell growth, proliferation, division, differentiation and malignant transformation. As the first rate-limiting enzyme in polyamine synthesis, ODC has a significant effect on polyamine levels. ODC is overexpressed in cancerous tissues from a number of malignancies, including gastric cancer, pancreatic cancer and colorectal cancer (5,6,14), and the inhibition of ODC may be a therapeutic strategy for malignancies, including breast cancer (15). It has been reported that the overexpression of ODC may lead to increased polyamine levels and thus induce the overproliferation and malignant transformation of cells (4,16–19). It contributes to the development, progression, metastasis and surrounding invasion of malignant tumors, and serves as a useful biological marker for certain precancerous lesions of digestive malignancies (4–8,16,17,20). A previous study demonstrated that Helicobacter pylori upregulates the expression of ODC, resulting in gastric precursor lesions and cancer (21). Carcinomas with highly expressed ODC are more progressive and poorly differentiated, with increased metastasis, surrounding invasion and poor prognosis. Hence, ODC may be a novel target for use in the development of new anticancer drugs and as an indicator for the efficacy of treatments (4–8,16,17,20).
Tissue-specific markers are useful for the identification of tumor type in advanced cancers of unknown origin. Jaraj et al investigated the expression of GAD67 (GAD1) in the prostate and found that GAD67 expression was significantly higher in malignant and benign prostatic tissue than in non-prostatic control tissues. It was suggested that GAD67 may serve as a highly prostate-specific tissue biomarker (22). However, whether GAD 65 (GAD2) plays a similar role in malignancies of the gallbladder remains unknown. In our study, we identified that GAD65 expression levels were significantly higher in gallbladder malignancy than in benign tissue.
Previous studies have shown that GABA stimulates the growth of a variety of types of cancer (23,24). The key enzyme for GABA synthesis is GAD which appears in two isoforms, GAD65 and GAD67, named according to their molecular weights (25). According to a study by Moon et al, the proliferation of HT-29 colon cancer cells was significantly inhibited when GAD67 expression was repressed (26). GAD65 is overexpressed in the cancerous tissues of numerous malignancies, including colon cancer, breast cancer and gastric cancer, and is closely associated with the clinicopathology of the diseases. Increased levels of GAD65 expression represent a more malignant, progressive and invasive nature of the lesion (11–13,27). The administration of a GABA receptor antagonist inhibits the growth and development of numerous types of cells, including malignant cells (9,10).
In the present study, the positive staining of ODC and GAD65 observed in gallbladder adenocarcinoma was significantly higher than in peritumoral tissues, adenomatous polyps and chronic cholecystitis. Furthermore, each case with expression of ODC and GAD65 was accompanied by mild, moderate or severe atypical proliferation of the gallbladder mucosal epithelium. As revealed in the present study, the expression levels of ODC and GAD65 in cases with adenoma canceration or well-differentiated carcinoma or without lymph node metastasis or surrounding invasion were significantly lower than those in cases with poorly differentiated carcinoma, lymph node metastasis or surrounding invasion. The expression levels of ODC and GAD65 in cases surviving >one year were significantly lower than those in cases succumbing to the disease within one year. Cox regression analysis revealed that the expression levels of ODC and GAD65 were ideal prognostic markers in gallbladder carcinoma. These results are in accordance with findings reported from previous studies. This suggests that ODC and GAD65 are closely correlated with the development, progression, metastasis and surrounding invasion of gallbladder adenocarcinoma and may be important biological markers for the early screening of gallbladder carcinoma in benign lesions and for the prognosis of gallbladder malignancy.
The authors would like to thank Professor Zhulin Yang for designing the study and examining the specimens.