MACC1 expression levels as a novel prognostic marker for colorectal cancer
- Authors:
- Published online on: August 19, 2014 https://doi.org/10.3892/ol.2014.2460
- Pages: 2305-2309
Abstract
Introduction
In developed countries where the aging population is increasing, cancer is one of the most prominent diseases with regard to public welfare and health measures. One in four mortalities in the USA, for example, is due to cancer (1). In the USA, the incidence of colorectal cancer (CRC) has increased significantly in recent years due to the changing lifestyle of the population and is currently one of the most frequently exhibited malignancies and leading causes of cancer-related mortality. The metastatic dissemination of primary tumors is directly associated with patient survival, and distant metastases, such as of the liver or lungs, are the major cause of mortality in CRC patients. Furthermore, metastatic disease is the most frequent reason for treatment failure (2). Therefore, the identification of genes that are responsible for the development and progression of CRC, and comprehension of the clinical significance of these genes is critical for the diagnosis and adequate treatment of CRC. The characterization of these key molecules is promising for the development of novel treatment strategies for CRC.
The hepatocyte growth factor (HGF)/mesenchymal-epithelial transition factor (MET) signaling pathway was reported to have a key role in cellular growth, invasiveness and metastasis (3–5). The metastasis-associated in colon cancer-1 (MACC1) induces MET expression and promotes HGF-induced scattering, which the mitogen-activated protein kinase (MAPK) signaling pathway prevents (6). This indicates that MACC1 expression in primary tumors is associated with metastasis and results in a poor prognosis.
The aim of the present study was to analyze the correlation between MACC1 expression levels, in tissue obtained from CRC patients, with their clinicopathological factors, and to investigate the possible functions of MACC1 in the metastasis of CRC.
Materials and methods
Clinical tissue samples
One hundred and seventy-four patients (99 males and 75 females) with CRC underwent curative surgery of CRC and distant metastases (if present) at the Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine and Medical Institute of Bioregulation at Kyusyu University (Osaka, Japan) between 1994 and 2003. No patients had received chemotherapy or radiotherapy prior to surgery. Primary CRC specimens and adjacent normal colorectal mucosa were obtained from patients following receipt of written informed consent, which was in accordance with the institutional ethical guidelines. The surgical specimens were fixed in formalin, processed through graded ethanol, and embedded in paraffin. The sections were stained with hematoxylin and eosin and Elastica van Gieson stain (Merck Millipore, Billerica, MA, USA), and the degree of histological differentiation, lymphatic invasion, and venous invasion was examined. Additionally, samples of each specimen were frozen in liquid nitrogen immediately after resection and stored at −80°C until RNA extraction. Following surgery, the patients underwent follow-up blood examinations to assess the tumor markers, serum carcinoembryonic antigen and cancer antigen 19–9 and imaging, such as abdominal ultrasonography, computed tomography and chest X-rays were conducted every 3–6 months. Postoperatively, stage III and IV patients received 5-fluorouracil-based chemotherapy [mFOLFOX6; 85 mg/m2 oxaliplatin and 2800 mg/m2 5-fluorouracil, for two weeks for a total of 12 courses of treatment; 300 mg/m2/day UFT, for 28 days for five weeks for five courses of treatment; 2500 mg/m2/day capecitabine for 14 days for three weeks for 8 courses of treatment, and/or 80 mg/m2/day TS-1 (tegafur, gimestat and otastat potassium) for 28 days for six weeks and four courses of treatment]. Adjuvant therapeutic strategies were performed, except for stage I and II patients who received no chemotherapy, according to the guidelines laid out by the Japanese Society for Cancer of the Colon and Rectum (7). Clinicopathological factors were assessed according to the tumor node metastasis (TNM) classification system of the International Union Against Cancer (8). This study was approved by the ethics committee of Osaka University Graduate School of Medicine (Osaka, Japan).
RNA preparation and expression analysis
Total RNA was prepared using TRIzol reagent (Invitrogen Life Technologies, Carlsbad, CA, USA) or using DNase and a modified acid guanidinium-phenol-chloroform procedure (9). Reverse transcription (RT) was performed with SuperScript™ II (Invitrogen Life Technologies) or by the methods reported previously (10) and an MACC1 fragment was amplified by polymerase chain reaction (PCR). Two human MACC1 oligonucleotide primers were designed as follows: Forward, 5′-TTCTTTTGATTCCTCCGGTGA-3′ and reverse, 5′-ACTCTGATGGGCATGTGCTG-3′. A PCR kit (Takara Ex Taq; Takara Bio Inc., Shiga, Japan) on a GeneAMP® PCR System 9600 (PE Applied Biosystems, Foster City, CA, USA) was used to perform 35 cycles of PCR with the following parameters: 95°C for 40 sec, 45°C for 40 sec and 72°C for 60 sec. An 8-μl aliquot of each reaction mixture was size-fractionated in a 1.5% agarose gel and visualized with ethidium bromide staining. To ensure the RNA was not degraded, a PCR assay with primers specific for the glyceraldehydes-3-phosphate dehydrogenase (GAPDH) gene was performed for 1 min at 95°C, 1 min at 56°C, and 1 min at 72°C for 30 cycles. The GAPDH primers were as follows: Forward, 5′-TTGGTATCGTGGAAGGACTCA-3′ and reverse, 5′-TGTCATCATATTGGCAGGTT-3′ and produced a 270-bp amplicon. Complementary DNA (cDNA) from Human Reference Total RNA (Clontech Laboratories, Mountain View, CA, USA) was analyzed concurrently and served as a positive control. For quantitative assessment, RT-qPCR was performed using a LightCycler® FastStart DNA Master SYBR Green I kit (Roche Diagnostics, Tokyo, Japan) for cDNA amplification of MACC1 and GAPDH. The amplification protocol consisted of 35 cycles of denaturation at 95°C for 10 sec, annealing at 60°C for 10 sec, and elongation at 72°C for 10 sec. The products were then subjected to a temperature gradient from 55°C to 95°C with continuous fluorescence monitoring to produce a melting curve of the products. The expression ratios of the MACC1 mRNA copies in the tumor and normal tissues were calculated following normalization against the GAPDH mRNA expression.
Statistical analysis
The association between MACC1 expression and patient clinicopathological factors was analyzed using the χ2 test. Kaplan-Meier survival curves were plotted and compared with the generalized log-rank test. Univariate and multivariate analyses were performed to identify prognostic factors using a Cox proportional hazards regression model. The in vitro assay values were analyzed using the Wilcoxon signed-rank test. All tests were analyzed with JMP software (SAS Institute Inc., Cary, NC, USA) and P<0.05 was considered to indicate a statistically significant difference.
Results
Expression levels of MACC1 in clinical tissue specimens
RT-qPCR analysis was performed on tissues from primary CRC and adjacent normal colorectal regions. MACC1 expression was calculated by normalising it to GAPDH expression for each tumor or normal tissue sample (Fig. 1). A significant difference was identified between the tissue types, with the average expression in tumor tissues larger than that of the corresponding normal tissues. In the following analyses, MACC1 expression, normalized to GAPDH expression, in tumor tissue was calculated following division by MACC1/GAPDH expression in the normal tissue.
Expression levels of MACC1 and patient clinicopathological characteristics
For the clinicopathological evaluation, experimental samples were divided into two groups according to the expression status. Patients with values >1 (MACC1 expression level of tumor tissue greater than that of the corresponding normal tissue) were assigned to the high-expression group and patients with values <1 were assigned to the low-expression group. The clinicopathological factors that were associated with the MACC1 expression status of the 174 patients are summarized in Table I. The data indicates that the level of MACC1 expression was not significantly correlated with the clinicopathological factors.
 | Table IClinicopathological factors and MACC1 mRNA expression in 174 colorectal cancer tissue samples. |
Association between MACC1 expression and prognosis
The data showed that the postoperative disease-free survival rate was significantly lower in patients in the high-expression group than that of the low-expression group (P=0.019; Fig. 2). The postoperative overall survival rate was lower in patients in the high-expression group than in the patients in the low-expression group (P=0.054; Fig. 3). The median follow-up was 4.1 years. Table II shows the results of the univariate and multivariate analyses for factors associated with disease-free survival. The univariate analysis showed that age (P=0.035), tumor invasion (P<0.001), lymph node metastasis (P<0.001), lymphatic invasion (P<0.001), venous invasion (P=0.011), distant metastasis (P<0.001) and MACC1 expression (P=0.005) were significantly correlated with disease-free survival. The multivariate regression analysis indicated in the MACC1 high-expression group (hazard ratio [HR], 2.27; 95% confidence interval [CI], 1.01–9.71; P=0.044), lymph node metastasis (HR, 3.15; 95% CI, 1.44–7.48; P=0.003), lymphatic invasion (HR, 2.87; 95% CI, 1.28–6.86; P=0.010) and distant metastasis (HR, 12.83; 95%; CI, 4.62–34.57; P<0.001) were independent predictors of disease-free survival.
| Table IIUnivariate and multivariate analyses for disease-free survival (Cox proportional hazards regression model). |
Discussion
HGF activates the HGF/MET signaling pathway, which is involved in metastasis of CRC. The HGF receptor, the gene for the receptor tyrosine kinase, MET was identified as the first transcriptional target of MACC1 (11). MACC1 is located on chromosome 7 and was identified through genome-wide expression analyses conducted on primary and metastatic colon cancer (12). MACC1 binds to, and promotes, MET gene expression by translocating from the cytoplasm to the nucleus, leading to migration, invasion and metastasis.
The present study demonstrated that MACC1 expression levels are an independent factor of disease-free survival for CRC. Tumor malignancy was identified to correlate with MACC1 expression levels and MACC1 expression may affect the values of other prognostic factors in multivariate analysis, such as distant metastasis, which was found to be significant in univariate analysis. MACC1 expression levels were a significant prognostic factor, reflecting disease-free survival as well as the occurrence of distant metastasis. The present study is considered to be important as it has provided analyses of a large number of samples, which demonstrate that MACC1 expression levels may be used as a statistically significant marker for CRC metastasis following curative resection, along with other reported predictors (13). The present results support recent reports that a MACC1-dependent signaling pathway is involved in the progression of CRC (12,14,15).
It is useful to determine the necessity for intensive follow-up and adjuvant CRC therapy by predicting recurrence and metastases following curative surgical resection (16–18). Certain patients respond well to the treatment of CRC, however others do not. Thus, more precise and personalized predictions and strategies for treating metastases are required (19). In the present study, the clinicopathological analysis of a large number of patients revealed that CRC samples exhibiting a low expression of MACC1 were an improved predictor for disease-free and overall survival when compared with the high-expression group. The data indicates that MACC1 expression levels are an effective predictor of CRC prognosis.
In CRC, various adjuvant chemotherapeutic strategies are facilitative during certain disease stages and indicate the usefulness of less invasive surgery for CRC (13,16–18,20–26). For these cases, an informative prognostic marker, which is independent from the traditional TNM classification and contributes to diagnosis and treatment, is important. In conclusion, the present data indicates MACC1 expression levels as a potential prognostic marker for CRC. Whilst improved preoperative and postoperative treatment strategies for CRC, such as chemo- and radiotherapy combined with surgery, have contributed to the reduction of recurrences, eventually half of the cases metastasize despite the systemic chemotherapy and surgery (27). Adjuvant chemotherapy for CRC is advantageous in cases where recurrence is considered to be likely. In these cases, MACC1 expression level analysis may present as a tool to predict poor prognosis and provide adequate treatment for patients.
