Expression of ASAP1 and FAK in gastric cancer and its clinicopathological significance

Abstract

The present study aimed to analyze the expression levels of adenosine diphosphate ribosylation factor guanylate kinase 1 (ASAP1) and focal adhesion kinase (FAK) in gastric cancer (GC) tissues in order to explore their association with clinicopathological features and prognosis. A total of 32 patients with GC were enrolled in the present study. All patients had complete clinical follow-up data and paraffin-embedded normal gastric mucosal tissues. The expression levels of ASAP1 and FAK in these tissues were measured by immunohistochemistry. The associations of ASAP1 and FAK expression with clinicopathological factors and the survival of patients with GC were subsequently analyzed. The expression levels of ASAP1 (59.4%) and FAK (68.8%) in GC tissues were significantly higher than those in normal gastric mucosal tissues (28.1 and 40.6%, P<0.05). The expression levels of ASAP1 and FAK were associated with depth of invasion, lymph node metastasis and pathological stage (P<0.05). ASAP1 expression was positively associated with FAK expression (P<0.001). In addition, ASAP1 and FAK expression levels were negatively associated with disease-free survival time and overall survival time (P<0.05). The 5-year overall survival rate was significantly higher in patients with negative ASAP1 or FAK expression compared with that in patients with positive ASAP1 or FAK expression (P<0.05). In conclusion, ASAP1 and FAK were highly expressed in human GC tissues and may serve a synergistic role in promoting tumorigenesis, progression, invasion and metastasis in patients with GC. ASAP1 and FAK expression in GC were associated with patient's survival. Therefore, ASAP1 and FAK may represent novel molecular markers for the pathophysiology and prognosis of GC.

Introduction

Gastric cancer (GC) is the fifth most common malignancy in the world with 951,600 new cases (6.8% of total) and 723,100 deaths (8.8% of total) in 2012 (1,2). Due to the non-specific symptoms of early-stage GC, and patients with advanced GC exhibit poor prognosis. Therefore, it is necessary to identify novel specific and sensitive biomarkers for GC that can assist in early diagnosis and improve its prognosis (3,4).

Adenosine diphosphate ribosylation factor guanylate kinase 1 (ASAP1) influences tumor cell migration and invasion, and therefore promotes the metastasis of tumor cells in the body. ASAP1 expression is significantly upregulated in various tumors and is closely associated with the malignant biological behavior and prognosis of these tumors (5–9). However, to the best of our knowledge, ASAP1 expression in GC and its association with GC prognosis have not been previously reported. Focal adhesion kinase (FAK) is an important non-receptor tyrosine kinase that influences cell proliferation, adhesion, invasion and migration, and is associated with tumor growth, anti-apoptotic mechanisms and tumor recurrence (10–12). Previous studies have demonstrated that FAK expression is upregulated in thyroid, esophageal, breast, gastric and intestinal cancer, and its expression is associated with a poor tumor prognosis (13,14). The present study used immunohistochemistry to detect the expression levels of ASAP1 and FAK in GC tissues, and analyzed their associations with multiple clinicopathological factors and with GC prognosis.

Materials and methods

Patients and tissue samples

All clinical GC tissue samples were isolated from 32 patients who had received a subtotal gastrectomy or radical total gastrectomy between December 2011 and February 2012 at the Union Hospital of Fujian Medical University (Fuzhou, China). The patients enrolled in the present study had not received radiotherapy or chemotherapy before surgery. In addition, all patients had complete follow-up data and available paraffin-embedded normal gastric mucosal tissues. The follow-up rate was 100%.

The clinical staging was evaluated based on the International Union Against Cancer (UICC) Tumor-Node-Metastasis (TNM) Classification of Malignant Tumors (15). Ethical approval for the present study was obtained from the Union Hospital of Fujian Medical University Ethics Committee. All patients or their guardians provided written informed consent.

Clinical information of the 32 patients is presented in Table I. There were 23 males and 9 females. The median age of the patients was 63.9 years (range, 40–87 years; patients ≥60 years, n=23; patients <60 years, n=9). Pathological findings indicated that 53.1% (n=17) of the tumors were classified as being moderately or highly differentiated, and 46.9% (n=15) as undifferentiated or poorly differentiated. A total of 22 patients (68.8%) presented with lymph node metastasis (N1-4). The depth of invasion was pT1+2 in 15 patients (46.9%) and pT3+4 in 17 patients (53.1%). A total of 14 patients (43.8%) were allocated to TNM stage I+II and 18 patients (56.3%) to stage III+IV.

Table I.

Clinicopathological characteristics of patients with gastric cancer.

Characteristic	n	%
Age, years
<60	9	28.13
≥60	23	71.88
Sex
Female	9	28.13
Male	23	71.88
Invasion depth
pT1+2	14	43.75
pT3+4	18	56.25
Lymph node metastasis
No	10	31.25
Yes	22	68.75
TNM stage
I+II	15	46.88
III+IV	17	53.12
Degree of differentiation
Moderate/high	17	53.12
Undifferentiated/low	15	46.88

pT1+2, tumor invades the submucosa or the muscularis propria; pT3+4, tumor invades the subserosa, non-peritonealised pericolic or perirectal tissues, or tumor directly invades other organs or structures and/or perforates the visceral peritoneum.

Disease-free survival (DFS) time was defined as the time from surgery to recurrence or mortality from any cause during the 5 years of follow-up. Overall survival (OS) time was defined as the time between initial surgery and the day of the last follow-up or mortality from any cause during the 5 years of follow-up. The mean 5-year DFS time was 77.37±35.08 months and the mean 5-year OS time was 77.57±34.02 months.

Immunohistochemistry

Serial 3-µm thick sections were cut from tissue samples, mounted onto glass slides, dewaxed in xylene and rehydrated in different concentrations (100, 95, 90, 85 and 70%) of ethanol. The sections were autoclaved in in citrate buffer (pH 6.0) at 121°C for 10 min for antigen retrieval. Samples were blocked with 5% normal goat serum (cat. no. KL-D1418; Kalang Biologicals) at 37°C for 30 min and then incubated with primary anti-ASAP1 (1:250; cat. no. 125729; Abcam) and anti-FAK (1:250; cat. no. 40794; Abcam) overnight at 4°C. Subsequently, samples were rinsed in PBS three times and incubated with a horseradish peroxidase-labeled secondary antibody (1:1,000; cat. no. K4003; Dako; Agilent Technologies, Inc.) at 37°C for 30 min. The slides were stained with 3,3′-diaminobenzidine (Dako; Agilent Technologies, Inc.) at room temperature for 2 min. Slides were washed in PBS three times. For color development: DAB color kit (cat. no. C520017; Sangon Biotech), reaction solution (10 ml) reagents A (200 µl) and reagents C (20 µl) were used to form the DAB color development solution. After rinsing with 50 µl extra water, the color development solution was added to each section in a dark place at 37°C for ~10 min. The sections were rinsed with purified water three times to terminate the color development. Hematoxylin (cat. no. E607318; Sangon Biotech) staining was performed at 37°C for 5 min and then counterstained with eosin (cat. no. E607318; Sangon Biotech) at 37°C for 30 sec. Slides were then dehydrated in 95% ethanol twice for 5 min each, and washed in xylene twice for 5 min each. Finally, sections were sealed using neutral balsam and left to dry naturally.

Immunohistochemistry scoring

Immunohistochemistry staining of ASAP1 and FAK was performed and scored by two experienced pathologists using a light microscope at ×200 magnification, according to a previous study published by Hou et al (5). The staining intensity was graded as follows: 0, unstained; 1, low signal (light yellow); 2, moderate signal (yellow brown); and 3, strong signal (brown). In addition, the score associated with the percentage of positive cells was assigned as follows: 0, <5% positive cells; 1, 5–10% positive cells; 2, 11–50% positive cells; 3, 51–80% positive cells; and 4, >80% positive cells. The final score was calculated by multiplying the scores associated with the percentage of positive cells by the score associated with the intensity. The scores were divided into the negative expression (final score, 0–4) and positive expression (final score, 6–12) groups.

Statistical analysis

All data were analyzed using SPSS v11.5 (SPSS Inc.). Quantitative data are presented as the mean ± SD, and qualitative data are presented as the rate or ratio. The survival time is presented as the median and quartiles. The χ² test or Fisher's exact test were used to analyze the differences among groups. The κ value was used to investigate the association between variables. Kaplan-Meier curves were used to evaluate the 5-year DFS rate or 5-year OS rate, and the log-rank test was used to analyze differences in survival rates. P<0.05 was considered to indicate a statistically significant difference.

Results

Protein expression of ASAP1 and FAK in GC tissues

The expression levels of ASAP1 and FAK were detected in GC tissues, and a brown/yellow signal was identified in the cytoplasm of positive cells by microscopy. Most of the positive cells for ASAP1 (Fig. 1A) and FAK (Fig. 1C) were found in tumor tissues. however, a limited number of cells presenting a low signal for ASAP1 (Fig. 1B) and FAK (Fig. 1D) were found in normal tissues adjacent to cancerous tissues. The positive expression rates of ASAP1 in 32 GC and normal gastric mucosal tissues were 59.4% (19/32) and 28.1% (9/32), respectively, and the difference was statistically significant (χ²=6.349; P=0.012). The positive expression rate of FAK was 68.8% (22/32) and 40.6% (13/32) in GC and normal gastric mucosal tissues, respectively, and the difference was statistically significant (χ²=5.107; P=0.024). As presented in Table II, the expression levels of ASAP1 and FAK in GC tissues were significantly associated with depth of invasion, lymph node metastasis, TNM stage and differentiation (P<0.05).

Figure 1.

Representative images of ASAP1 and FAK protein expression in GC tissues. (A) Positive expression of ASAP1 in GC tissues. ASAP1 expression in GC tissues was positive, with a brown/yellow signal detected in the cytoplasm, as assessed by microscopy. (B) Negative expression of ASAP1 in paraneoplastic tissues. Cytoplasmic signal for ASAP1 was negative in normal tissues adjacent to the cancer. (C) Positive expression of FAK in GC tissues. FAK expression in GC tissues was positive, with a brown/yellow signal detected in the cytoplasm, as assessed by microscopy. (D) Negative expression of FAK in paraneoplastic tissues. Cytoplasmic staining of FAK was negative in normal tissues adjacent to the cancer. Magnification, ×200. GC, gastric cancer; ASAP1, adenosine diphosphate ribosylation factor guanylate kinase 1; FAK, focal adhesion kinase.

Table II.

Association between ASAP1 and FAK expression and clinicopathological features of patients with gastric cancer (n=32).

	ASAP1			FAK
Characteristic	−, n	+, n	P-value	−, n	+, n	P-value
Age, years
<60	6	3	0.109	4	5	0.407
≥60	7	16		6	17
Sex
Female	5	4	0.427	4	5	0.407
Male	8	15		6	17
Invasion depth
pT1+2	11	3	<0.001	9	5	0.001
pT3+4	2	16		1	17
Lymph node metastasis
No	8	2	0.005	7	3	0.003
Yes	5	17		3	19
TNM stage
I+II	11	4	0.001	9	6	0.002
III+IV	2	15		1	16
Degree of differentiation
Moderate/high	13	4	<0.001	10	7	<0.001
Undifferentiated/low	0	15		0	15

Data were analyzed by Fisher's exact probability test. pT1+2, tumor invades the submucosa or the muscularis propria; pT3+4, tumor invades the subserosa, non-peritonealised pericolic or perirectal tissues, or tumor directly invades other organs or structures and/or perforates the visceral peritoneum; -, negative; +, positive; ASAP1, adenosine diphosphate ribosylation factor guanylate kinase 1; FAK, focal adhesion kinase.

Association between ASAP1 and FAK expression in GC tissues

Among the 19 GC tissues with positive ASAP1 expression, 19 were positive for FAK (100.0%). Among the 13 GC tissues with negative ASAP1 expression, 3 were positive for FAK (23.1%). κ analysis indicated that the expression levels of ASAP1 were associated with FAK expression in GC tissues (κ=0.798; P<0.001; Table III).

Table III.

Association between ASAP1 and FAK expression in gastric cancer tissues.

	FAK expression
ASAP1 expression	positive	negative	Total	κ	P-value
Positive	19	0	19	0.798	<0.001
Negative	3	10	13
Total	22	10	32

ASAP1, adenosine diphosphate ribosylation factor guanylate kinase 1; FAK, focal adhesion kinase.

Association between ASAP1 expression, FAK expression and GC prognosis

The Kaplan-Meier survival curve analysis revealed that ASAP1 and FAK expression levels were negatively associated with 5-year DFS time in patients with GC. The 5-year DFS rate was 57.9% (11/19) in the ASAP1-positive group and 92.3% (12/13) in the negative group. The difference was statistically significant (log-rank χ²=4.721; P=0.030; Fig. 2A). The 5-year DFS rate was 63.6% (14/22) in the FAK-positive group and 90.0% (9/10) in the negative group. The difference was not statistically significant (log-rank χ²=2.472; P=0.116; Fig. 2B).

Figure 2.

Survival curves of gastric carcinoma generated by the Kaplan-Meier method and the log-rank test. (A) Association between ASAP1 expression and 5-year DFS time. The 5-year DFS rate was lower in the ASAP1-positive group compared with that in the ASAP1-negative group (log-rank χ²=4.721, P=0.030). (B) Association between FAK expression and 5-year DFS time. The 5-year DFS rate was lower in the FAK-positive group than that in the FAK-negative group (log-rank χ²=2.472, P=0.116). (C) Association between ASAP1 expression and 5-year OS time. The 5-year OS rate was lower in the ASAP1-positive group than that in ASAP1-negative group (log-rank χ²=7.988, P=0.005). (D) Association between FAK expression and 5-year OS time. The 5-year OS rate was lower in the FAK-positive group than that in the FAK-negative group (log-rank χ²=5.092, P=0.024). OS, overall survival; DFS, disease-free survival; ASAP1, adenosine diphosphate ribosylation factor guanylate kinase 1; FAK, focal adhesion kinase.

The 5-year OS rate of patients with positive and negative ASAP1 expression was 52.8% (10/19) and 100.0% (13/13), respectively, and the difference was statistically significant (log-rank χ²=7.988; P=0.005; Fig. 2C). The 5-year OS rate of patients with positive and negative FAK expression was 59.1% (13/22) and 100.0% (10/10), respectively, and the difference was statistically significant (log-rank χ²=5.092; P=0.024; Fig. 2D).

Discussion

GC is one of the most common malignant tumors that poses a severe threat to human health. Genome-driven targeted cancer therapies may provide novel and promising strategies for cancer prevention and control (16). In 2009, the American Society of Clinical Oncology reported the first targeted therapy for GC in the ‘trastuzumab for gastric cancer trial’, demonstrating that trastuzumab combined with chemotherapy as first-line treatment may improve the survival of human epidermal growth factor receptor 2 (HER2)-positive patients with advanced GC (17). However, the global positive rate of HER2 in advanced GC is only 25%, and half of these patients exhibit a poor response to trastuzumab due to unknown causes (18). To the best of our knowledge, the only first-line targeted drug for GC is trastuzumab, the only second-line drug is ramucirumab and the only third-line drug is apatinib (19). Therefore, the available targeted treatments for GC are limited compared with those for other types of cancer, and further studies are required to develop novel therapeutic strategies to improve GC treatment.

ASAP1 is a phospholipid-dependent GTPase-activating protein (GAP) located on the long arm of chromosome 8, at 24.1–24.2. As a member of the ARF GAP family, ASAP1 hydrolyzes GTP to regulate actin re-organization and actin cytoskeletal dynamics, in this way controlling motility, regulating the formation of focal adhesions and invasive pseudopods, and contributing to the folding of the plasma membrane (20–24). In addition, ASAP1 binds to the SH3 domain-containing kinase-binding protein 1, the CD2-associated protein, cortactin, the CRK-like proto-oncogene adaptor protein and the SRC proto-oncogene non-receptor tyrosine kinase through its structural domains to exert its biological activities and to regulate cell invasion (25–27). Recent studies have described the association between ASAP1 and the biological features of malignant tumors. Müller et al (20) demonstrated that ASAP1 promotes the invasion of colorectal cancer cells in vitro and stimulates the metastasis of colorectal cancer cells in vivo. Hou et al (5) revealed that ASAP1 expression in ovarian cancer tissues is significantly higher than that in normal ovarian tissues. In-depth analysis has demonstrated that positive ASAP1 expression is an indicator of poor prognosis in ovarian cancer and is an independent prognostic factor for the OS rate of patients with ovarian cancer. In addition, Liu et al (28) demonstrated that downregulation of ASAP1 expression by RNA interference inhibits cell proliferation and migration. However, to the best of our knowledge, no previous studies have investigated ASAP1 expression in GC tissues. In the present study, the expression levels of ASAP1 in GC tissues were significantly higher than those in tumor-adjacent normal gastric mucosal tissues (P=0.012). ASAP1 expression in GC tissues from patients with a T3+T4 infiltration depth was higher compared with that in patients with a T1+T2 infiltration depth (P<0.001). Furthermore, ASAP1 expression in GC tissues from patients with lymph node metastasis was higher than that of patients without lymph node metastasis (P=0.005). ASAP1 expression in GC tissues from patients at stages III and IV was significantly higher than that of patients at stages I and II (P=0.001). Compared with moderate or higher degree of differentiation, patients with undifferentiated or lower degree of differentiation had a higher ASAP1 expression levels (P<0.001). The DFS rates of patients with positive and negative ASAP1 expression were 57.9% (11/19) and 92.3% (12/13), respectively, with a significant difference between the two groups (P=0.030). The OS rates of patients with positive and negative ASAP1 expression were 52.8% (10/19) and 100.0% (13/13), respectively, with a significant difference between the two groups (P=0.005). Therefore, the present results suggested that ASAP1 may serve important roles in the growth, invasion and metastasis of malignant gastric tumors, and may represent a novel molecular marker for evaluating the biological behavior and prognosis of GC.

FAK was first identified and cloned by Schaller et al (29) from v-src-transfected chicken embryo fibroblasts in the 1990s. The human FAK gene is located on the long arm of chromosome 8 (8q24). The FAK protein is a non-receptor tyrosine protein kinase with six tyrosine sites that can be phosphorylated: Tyr397 and Tyr407 are located at the amino terminus, Tyr576 and Tyr577 are located in the activation loop of the kinase domain, and Tyr861 and Tyr925 are located at the carboxyl terminus. Activated FAK participates in tumor proliferation, growth, invasion and metastasis via multiple signaling pathways, such as the FAK-Ras-PK, FAK-PI3K and FAK-STAT pathways (12). A study by Weiner et al (30) published in 1993 revealed that FAK expression is increased in invasive tumors and that positive FAK expression is present in all metastatic tumors, suggesting that it may promote tumor cell invasion and metastasis. A study by Miyazaki et al (31) published in 2003 demonstrated that FAK upregulation is associated with infiltration depth, lymph node metastasis and the number of metastatic lymph nodes in esophageal cancer. In 2010, Park et al (32) used immunohistochemistry to detect FAK expression in 444 surgically resected GC tissues. Additionally, a study by Lai et al (33) revealed that FAK can be autophosphorylated at the 397-tyrosine residue and that after this activation it initiates processes such as the proliferation, invasion and migration of GC cells. A study by Fan et al (11) in 2013 demonstrated that FAK activation increases endogenous A2 protein phosphorylation and leads to changes in epithelial-mesenchymal transition markers, including matrix metalloproteases, thereby inducing tumorigenesis and tumor progression. A study by Wang et al (34) in 2019 revealed that FAK binds directly to microRNA-1224 to inhibit the activation of the STAT3 and NF-κB pathways, thereby suppressing the metastasis of GC. The present results suggested that the expression levels of FAK in GC tissues were significantly upregulated compared with those in tumor-adjacent normal gastric mucosal tissues (P=0.024). Additionally, FAK expression was associated with depth of infiltration, lymph node metastasis, increased tumor stage and decreased differentiation degree. The OS rates of patients with positive and negative FAK expression were 59.1% (13/22) and 100.0% (10/10), respectively, with a significant difference between the two groups (P=0.024). The present results suggested that FAK may serve a role in the tumorigenesis and progression of GC. Abnormal FAK expression may lead to more malignant GC cell proliferation, growth, invasion and metastasis. Therefore, FAK may be useful as a novel molecular marker to evaluate the biological behavior and prognosis of GC.

ASAP1 is a multi-domain protein with rich in proline structural regions which binds to various structural proteins to exert its biological function. ASAP1 interacts with non-muscle myosin II-A to regulate actin cytoskeleton remodeling and the transport of integrin, thereby affecting cell invasion and metastasis (35,36). FAK, as a key molecule in integrin-dependent signal transduction pathways, serves an important role in the binding between integrin and ligands, thus promoting the formation of focal adhesions (37). A study by Liu et al (28) used yeast two-hybrid screening and a co-immunoprecipitation assay to demonstrate a direct interaction between ASAP1 and FAK. In the present study, 29 samples were found to co-express ASAP1 and FAK in GC tissues, which resulted in a κ value of 0.798 (P<0.001), indicating that ASAP1 expression was associated with FAK expression and that ASAP1 and FAK promoted the pathophysiology of malignant GC. The present results suggested an association between ASAP1 and FAK, which affected the pathophysiology of malignant GC. Therefore, ASAP1 may promote the malignant phenotype of GC cells through FAK.

In conclusion, ASAP1 and FAK were highly expressed in GC tissues and were associated with degree of invasion, lymph node metastasis, pathological staging and degree of differentiation in the present study. In addition, positive expression of ASAP1 and FAK may be risk factors for the prognosis of patients with GC. The present findings suggested that ASAP1 and FAK may synergistically promote the tumorigenesis, tumor progression, invasion and metastasis of GC, and are closely associated with the survival of patients with GC. Although the sample size was too small, which was one of the limitations of the present study, it provided a basis for a follow-up study on the association between ASAP1, FAK and GC. ASAP1 and FAK may represent novel molecular markers for the pathophysiology and prognosis of GC. In addition, further in vitro and in vivo studies investigating the molecular mechanisms of ASAP1 and FAK in the tumorigenesis and tumor progression of GC may help to elucidate the pathophysiology of malignant GC. Furthermore, additional studies may provide important information for the early diagnosis, treatment and prognostic assessment of GC, as well as novel molecular targets and therapeutic strategies to develop novel drugs to treat GC.

Funding

The present study was partially supported by the Health- Education Joint Research Project of Fujian Province (grant no. WKJ2016-223), the Science Technology Innovation Joint Project Foundation of Fujian Province (grant no. 2017Y9003), the Startup Fund for Scientific Research, Fujian Medical University (grant no. 2017XQ2037), the Science Technology Innovation Joint Project Foundation of Fujian Province (grant no. 2018Y9038) and the Program for Innovative Research Team in Science and Technology in Fujian Province University.

Availability of data and materials

The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.

Authors' contributions

SY and XC conceived and supervised the project. QL, SZ, DZ and FY performed the experiments and analyzed the data. QL, SZ and DZ wrote the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Ethical approval for the present study was obtained from the Union Hospital of Fujian Medical University Ethics Committee (Fuzhou, China). All patients or their guardians provided written informed consent.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.