Expression of deleted in liver cancer 2 in colorectal cancer and its correlation with clinicopathological parameters

Abstract

Deleted in liver cancer 2 (DLC2) has been identified as a tumor suppressor gene. DLC2 is closely related to deleted in liver cancer 1 (DLC1) and is located at chromosome 13q12.3. The expression of DLC2 mRNA has been found in a wide range of cancers, including colorectal cancer (CRC). However, there are no available data on the expression status of DLC2 in Chinese patients with CRC and its correlation with clinicopathological parameters. The aim of this study was to investigate the expression levels of DLC2 mRNA and protein in Chinese patients with CRC and the correlation between DLC2 expression and clinicopathological parameters. To this end, real-time PCR, western blotting and immunohistochemistry were employed to detect DLC2 mRNA and protein expression in CRC and pericarcinomatous intestinal tissue (PCIT) specimens, which were obtained from 102 Chinese CRC patients who underwent surgical resection between October 2010 and February 2012. We also analyzed the correlations between DLC2 expression and the clinicopathological parameters of CRC patients. Our results showed that CRC tissues had significantly lower levels of DLC2 mRNA compared with PCITs (P<0.05); however, the protein expression levels were not significantly different between CRCs and PCITs. The expression levels of DLC2 mRNA and protein were significantly correlated with lymph node metastasis and tumor TNM stage. Additionally, DLC2 mRNA expression levels were also correlated with tumor histopathological degree (P<0.05). Collectively, our results suggest that the downregulated expression of DLC2 participates in CRC carcinogenesis, invasion and lymph node metastasis. Furthermore, our results imply that DLC2 is be a potential prognostic marker for CRC patients.

Introduction

Colorectal cancer (CRC) is one of the most common malignant tumors, with 1,200,000 new cases and 608,700 mortalities worldwide annually (1); furthermore, it is the fourth leading cause of cancer-related mortality in China. In recent decades, the incidence of CRC has increased. Despite surgical resection coupled with systemic chemotherapy, approximately half of newly diagnosed CRC patients are likely to succumb to the disease due to tumor recurrence and metastasis (2). The molecular mechanism leading to the development, local invasion and distal metastasis of CRC remains unclear. Thus, the delineation of the mechanisms for colorectal carcinogenesis is of importance, as it may provide novel strategies for diagnosis and prognosis.

Deleted in liver cancer 2 (DLC2), also called STARD 13, has been identified as a tumor suppressor gene and is closely related to deleted in liver cancer 1 (DLC1). DLC2 is located at chromosome 13q12.3 (3). DLC1 and DLC2 proteins share 51% identity and 64% similarity at the level of their amino acid sequences. DLC2 protein contains multiple domains, including a sterile α motif (SAM), a RhoGAP and a lipid-binding StAR-related lipid-transfer (START) domain. Previous studies have shown that DLC2 suppressed cytoskeleton reorganization, cell growth, cell migration and transformation in hepatocellular carcinoma (HCC) (4); the START domain of DLC2 has been reported to be involved in mitochondrial localization in hepatoma cells (5) and our previous study indicated that patients with DLC2 underexpression showed a significantly poorer prognosis than those with high DLC2 expression in HCC (6). To date, all studies examining DLC2 expression and its suppressed function have been conducted on HCC. However, DLC2 mRNA has been found to be downregulated in a wide range of cancers, including CRC (7), but there have been no available data on the expression levels of DLC2 mRNA and protein in clinical CRC, especially in Chinese patients.

Therefore, in this study we examined the DLC2 mRNA and protein expression in Chinese patients with CRC and evaluated the correlations between DLC2 expression levels and clinicopathological parameters of CRC.

Materials and methods

Tissue specimens

The study protocol was approved by the Ethics Committee of the Central South University (CSU). Fresh samples of CRC tissues and pericarcinomatous intestine tissues (PCITs, 2.0 cm away from the carcinoma) were obtained from 102 (66 males and 36 females) Chinese patients with primary cancer who underwent surgery at The Third Affiliated Hospital of Central South University between Octorber 2010 and February 2012. Each specimen was divided into two parts; one was immediately frozen in liquid nitrogen and stored at −80°C for real-time PCR and western blot analysis, the other was fixed in 4% paraformaldehyde for immunohistochemistry. The median age of the patients was 55.43 years, ranging from 26 to 78 years. All specimens obtained from surgical resection were confirmed by pathological examination. Written informed consent was obtained from each patient prior to the study.

Real-time PCR

Total RNA was extracted from specimens using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. Aliquots of 5 μg RNA from each sample were reverse transcribed. Quantitative analysis of DLC2 mRNA expression using the SYBR Green method was performed using the ABI 7300 real-time PCR system. The sequences of the primers were as follows: DLC2 5′-GTCAATGGGCTCCAAGAGGTAG-3′ (forward) and 5′-TGATTAGGAGATGGAAAGGTGGA-3′ (reverse); GAPDH (endogenous control): 5′-CTGCACCACCAACTG CTTAG-3′ (forward); 5′-AGGTCCACCACTGACACGTT-3′ (reverse). A 25-μl reaction mixture containing 1 μl cDNA template, 12.5 μl SYBR Master mix and 0.20 μl of each primer was amplified using the following thermal parameters: denaturing at 95˚C for 10 min and 45 cycles of the amplification step (denaturation at 95˚C for 15 sec, annealing and extension at 60˚C for 1 min). All amplification reactions were performed in triplicate and the averages of the threshold cycles (Cts) were used to interpolate curves using 7300 System SDS software. The results were expressed as the ratio of DLC2 mRNA to GAPDH mRNA, and the results of each sample was compared against one control sample to eliminate the differences between the PCR plates.

Western blot analysis

Protein was extracted from the specimens using the fierce RIPA lysis buffer (Beyotime Biotech, Jiangsu, China) following the manufacturer's instructions. Briefly, an equal amount (35 μg) of the total protein was separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE; Beyotime Biotech) and then transferred onto a polyvinylidene difluoride (PVDF; Pall, NY, USA) membrane using standard procedures. The membranes were immunoblotted with antibodies against DLC2 (rabbit polyclonal antibody; Sigma, St. Louis, MO, USA), followed by a horseradish peroxidase-conjugated secondary antibody. The washes were repeated before the membranes were detected using ECL system (KPL Biosciences, Gaithesburg, MD, USA). Band intensities were analyzed densitometrically using the Image J software.

Immunohistochemistry

All the specimens were immunohistochemically evaluated. In brief, tissue sections of 3-μm thickness were cut and baked at 60˚C, deparaffinized in xylene and rehydrated through graded ethanol. Next, 3% hydrogen peroxide and methanol were applied to block the endogenous peroxidases and sections were subjected to heat-induced antigen retrieval in 0.01 M citrate buffer (pH=6.0). The samples were incubated overnight with primary antibodies against DLC2 at a 1:400 dilution (rabbit polyclonal antibody; Sigma). Then, the samples were treated with MaxVision TM HRP-Polymer anti-Mouse/Rabbit IHC kit (KIT-5020, MaxVision, Shenzen, China) and 3,3′-diaminobenzidine tetrahydrochloride (DAB). Counterstaining was performed with 0.5% hematoxylin.

Statistical analysis

Statistical analysis was performed using SPSS software (version 17.0; SPSS, Inc., Chicago, IL, USA). Data are expressed as mean ± SD and, for clarity, as mean ± SEM in figures. The Student's t-test was used to analyze the correlation betwen the expression of DLC2 in CRC and PCIT. The non-parametric Mann-Whitney U test was used to analyze the correlations between the expression of DLC2 and clinicopathological variables. P<0.05 was considered to indicate a statistically significant result.

Results

Expression of DLC2 mRNA in CRC and PCIT

The expression of DLC2 mRNA was detected in all CRC and PCIT specimens using real-time PCR. The relative expression of DLC2 mRNA in CRC and PCIT was 29.16±5.36 and 65.87±17.05, respectively. The mRNA expression in CRC tissues was significantly lower than that in PCIT (P=0.037; Fig. 1).

Figure 1.

Expression of DLC2 mRNA in CRC and PCIT. The mRNA expression in CRC was significantly lower than that in PCIT (mean ± SEM, n=102), ^*P<0.05 compared with CRC. DLC2, deleted in liver cancer 2; CRC, colorectal cancer; PCIT, pericarcinomatous intestinal tissue.

Expression of DLC2 protein in CRC and PCIT

The protein expression was detected in all CRC and PCIT specimens using western blotting. The relative expression of DLC2 protein in CRC and PCIT was 2.29±0.61 and 1.66±0.65, respectively. There was no significant difference between CRC and PCIT. In addition, to identify the DLC2 protein expression status, immunohistochemical staining was also employed. The result was consistent that of the western blot analysis (Fig. 2).

Figure 2.

Expression of DLC2 was detected in CRC and PCIT deparaffinized specimens by immunohistochemistry. (A) Positive expression of DLC2 in CRC. (B) Negative expression of DLC2 in CRC. (C) Positive expression of DLC2 in PCIT. (D) Negative expression of DLC2 in PCIT. DLC2, deleted in liver cancer 2; CRC, colorectal cancer; PCIT, pericarcinomatous intestinal tissue.

Correlations between DLC2 expression levels and clinicopathological parameters of CRC

The distribution pattern of DLC2 was determined by dividing the expression levels of DLC2 mRNA and protein in the subgroups by clinicopathological parameters. A significant difference was found between DLC2 expression levels in CRC with or without lymph node metastasis (P= 0.021 and 0.028, respectively); both DLC2 mRNA and protein expression levels in CRC with lymph node metastasis were lower than those in CRC cases without lymph node metastasis (Figs. 3A and 4A). DLC2 mRNA and protein expression levels of CRC of tumor TNM stage III and IV also showed lower expression levels than in CRC cases of stage I and II (P=0.020 and 0.026, respectively; Figs. 3B and 4B). In addition, the expression status of DLC2 mRNA was also correlated with tumor histopathological degree; poorly differentiated CRC cases had a lower expression level of DLC2 than well- and moderately differentiated CRC (P= 0.004; Fig. 5). However, there was no significant association between the expression levels of DLC2 and other clinicopathological parameters, including gender, age, tumor size, tumor site, depth of cancer invasion, distant metastasis and blood levels of carcinoembryonic antigen (CEA; Table I).

Figure 3.

Correlation between DLC2 mRNA expression and lymph node metastasis and between DLC2 mRNA expression and tumor TNM stage. (A) N (−), lymph node metastasis-negative (mean ± SEM, n=50); N (+), lymph node metastasis-positive (mean ± SEM, n=52); ^*P<0.05 compared with N (−). (B) I+II, TNM stage I and II (mean ± SEM, n=49); III+IV, TNM stage III and IV (mean ± SEM, n=53); ^*P<0.05 compared with I +II. DLC2, deleted in liver cancer 2.

Figure 4.

Correlation between DLC2 protein expression and lymph node metastasis and between DLC2 protein expression and tumor TNM stage. (A) N (−), lymph node metastasis-negative (mean ± SEM, n=50); N (+), lymph node metastasis-positive (mean ± SEM, n=52); ^*P<0.05 compared with N (−). (B) I+II, TNM stage I and II (mean ± SEM, n=49); III+IV, TNM stage III and IV (mean ± SEM, n=53); ^*P<0.05 compared with I+II. DLC2, deleted in liver cancer 2.

Figure 5.

Correlation between DLC2 mRNA expression and tumor histopathological degree. Poor, poorly differentiated CRC (mean ± SEM, n=26); Well + moderate, well- and moderately differentiated CRC (mean ± SEM, n=76). ^*P<0.05 compared with well + moderate. DLC2, deleted in liver cancer 2; CRC, colorectal cancer.

Table I.

Correlation between expression levels of DLC2 and clinicopathological parameters.

Variable	No. of patients	P-value
		DLC2 mRNA	DLC2 protein
Gender		0.429	0.288
Male	66
Female	36
Age (years)		0.625	0.420
<60	60
≥60	42
Tumor site		0.528	0.918
Colon	45
Rectum	57
Tumor size (cm)		0.457	0.425
<5.0	52
≥5.0	50
Tumor depth		0.876	0.354
Limited to muscular layer	66
Serosa and adjacent fat	36
Lymph node metastasis		0.021a	0.028a
Negative	50
Positive	52
Distant metastasis		0.338	0.233
Absent	94
Present	8
Tumor TNM stage		0.020a	0.026a
I and II	49
III and IV	53
Tumor differentiation		0.004a	0.080
Well-moderate	76
Poor	26
CEA (ng/ml)		0.903	0.271
≥5	41
<5	61

^aP<0.05. DLC2, deleted in liver cancer 2; CEA, carcinoembryonic antigen.

Discussion

Although DLC2 has been identified as a tumor suppressor gene, the expression levels of DLC2 mRNA and protein, especially in clinical CRC of Chinese patients, have not been studied. The present study indicates that the expression level of DLC2 mRNA was significantly lower in CRC than in PCIT; however, the protein expression level of DLC2 was not significantly different in CRC compared with PCIT in Chinese patients. This difference between mRNA and protein may be due to post-transcriptional control. With regard to human neoplasia, Ullmannova and Popescu reported that the DLC2 mRNA level was downregulated in lung, ovarian, renal, breast, uterine, gastric, colon and rectal tumors and that the expression ratios of DLC2 in colon and rectal cancer were 46 and 61%, respectively (7). Our real-time PCR results showed that DLC2 mRNA was also underexpressed and the expression ratios of DLC2 mRNA were 70 and 62% in colon and rectal cancer, respectively. This result is higher than that reported by Ullmannova and Popescu; the reason for this difference may be differences between ethnicities. Also, the low expression of DLC2 has been confirmed to be involved in the invasion and migration of HCC cells (4). DLC2 protein has been reported to inhibit the activity of Raf-1-ERK1/2-p70S6K via its RhoGAP function, resulting in the suppression of cell growth (8). DLC2 has been found to modulate angiogenic responses in vascular endothelial cells by regulating cell attachment and migration (9). Consistent with previous studies, the present study showed that DLC2 mRNA was downregulated in CRC, which indicates that DLC2 participates in colorectal carcinogenesis and plays an important role in the invasion and metastasis of CRC.

To investigate how DLC2 affects colorectal carcinogenesis, we evaluated the correlations between DLC2 expression levels, including mRNA and protein, and clinicopathological parameters of CRC. Our results revealed that the expression levels of DLC2 mRNA and protein were frequently with lymph node metastasis and the DLC2 expression levels in CRC with lymph node metastasis were lower than those in CRC without lymph node metastasis. This result indicates that DLC2 is a tumor suppressor, whose downregulated expression stimulates the lymph node metastasis of CRC. This implies that DLC2 has a role in suppressing CRC lymph node metastasis. Our previous study showed that a lower expression level of DLC2 was associated with higher expression level of RhoA in HCC (6). In addition, other studies have shown that DLC2 exhibited its tumor suppressor functions by means of the inhibition of RhoA activity (4); a higher level expression of RhoA has been detected in several types of cancer, including bladder, testicular, ovarian, colon, breast and lung cancer (10–13); Takami et al demonstrated that the activity of RhoA was correlated with lymph node metastasis in human CRC (14). Accordingly, we hypothesized that the downregulation of DLC2 and upregulation of RhoA may be essential in CRC progression, especially in the process of CRC lymph node metastasis. To confirm this hypothesis, investigations into the correlation between DLC2 and RhoA are anticipated.

Notably, in the present study, the mRNA and protein expression levels of DLC2 were also correlated with CRC tumor TNM stage. Our results revealed that the DLC2 mRNA and protein expression levels in CRC of TNM stages III and IV were lower than those in CRCs of stage I and II. This result implies that downregulated mRNA and protein expression levels of DLC2 were correlated with advanced stage of CRC. Additionally, the mRNA expression level was correlated with tumor histopathological degree of CRC. It is well known that the TNM staging system of tumors is the gold standard for evaluating prognosis in patients with CRC. It has been reported that the five-year survival rates of CRC patients who underwent surgical resections were 94.1, 80.2, 61.7 and 23.2% with tumors of TNM stages I to IV, respectively (15); additionally, low tumor histopathological differentiation was also associated with poor survival (16). Thus, it is reasonable to assume that the downregulated expression of DLC2 is correlated with a poor prognosis of CRC patients. To test this assumption, we intend to continue the follow-up of these patients in our further research.

To the best of our knowledge, this is the first study to report DLC2 mRNA and protein expression levels in Chinese CRC patients and the downregulated expression levels of DLC2 mRNA and protein are associated with lymph node metastasis and tumor TNM stage in CRC. The DLC2 mRNA expression level is also correlated with tumor histopathological degree. Although a number of diagnostic advances have been made, it remains difficult to accurately diagnose lymph nodes metastasis and assess the prognosis of CRC. In this study, we found that the downregulated expression levels of DLC2 mRNA and protein were correlated with lymph node metastasis and tumor TNM stage. Furthermore, the underexpression of DLC2 mRNA was also associated with tumor histopathological degree of CRC. Therefore, the present study demonstrates that DLC2 may not only participate in CRC carcinogenesis, invasion and lymph node metastasis, but may also be a potential indicator for the presence of lymph nodes metastasis in CRC and a prognostic marker for CRC patients.