Activation of P21-activated protein kinase 2 is an independent prognostic predictor for patients with gastric cancer

Gastric cancer is one of the most common neoplasms in digestive system with highly malignant and a poor prognosis worldwide, especially in Asia and Africa[1]. It tends to be associated with lymph node metastasis, peritoneal dissemination, and hematogenous metastasis. Despite the advancement of surgical technique and the improvement of anticancer drugs in recent years, gastric cancer is still a leading cause of cancer-related deaths and the 5-year survival rate is approximately 20%[2]. Especially in China, the morbidity of gastric cancer has reached to second with 3,621,000 new cases, whilst the mortality rate ranked third with the proportion of 14.33% annually[3]. It has been demonstrated that the depth of tumor invasion, peritoneal dissemination, hepatic metastasis, and lymph node metastasis are significant factors in determining prognosis[4]. Since tumor invasion and metastasis are very complicated and continuous processes involving multiple steps, regulated at the molecular level by adhesion molecules, protein catabolic enzymes, cellular growth factors, and various angiogenic factors, it is extremely necessary to identify novel and efficient biomarkers for the evaluation of the behavior in tumor development and metastasis in order to predict prognosis and improve therapeutic strategies for patients with gastric cancer.

The p21-activated kinases (PAKs) are a family of serine/threonine protein kinases, which were initially identified as binding partners of the Rho GTPases Cdc42 and Rac1[5]. The PAK family includes six isoforms (PAK1-6) which play a crucial role in a variety of physiological processes such as motility, survival, mitosis, apoptosis, and hormone signaling[6]. The PAKs are divided into two groups, group I (PAKs 1–3) and group II (PAKs 4–6) based on structural and functional similarities: group I PAKs exist in an inactive homodimer maintained by interactions between the autoinhibitory domain (AID) and kinase domain of PAK monomers; group II PAKs also bind Rac and Cdc42, but they lack an AID, exist as active monomers, and have not been reported to have a scaffolding function[7]. Recent studies have demonstrated that PAKs are overexpressed, hyperactivated or amplified in several human cancers and their role in cell transformation make them attractive therapeutic targets[8]. Especially, PAK2, which has an overall 76% homology with PAK1 and 96% homology in the kinase domain, has a dual role in both cell survival and cell death pathways. It is widely distributed throughout the body and is not only activated by binding with the small G protein complex Cdc42/Rac, but it is also cleaved and activated by caspase-3 and similar proteases[9]. Full length PAK2 is autophosphorylated at eight sites including Ser20, Ser139, Ser141, Ser144, Ser192, Thr402, Thr421 and Thr423, and then activated[9]. Accumulating evidence indicates that PAK2 are either up-regulated or hyperactivated in a variety of human cancers, including ovarian cancer[10] and breast cancer[11]. PAK2 plays an important role in tumor aggressiveness, but its involvement in gastric cancer has not yet clear. The aim of this study was to investigate whether PAK2 expression and its phosphorylation status are correlated with tumor progression and prognosis in gastric cancer.

Gastric cancer patients with the same tumor stage present different clinical courses and have different prognosis. This heterogeneity is present at the molecular level and has a genetic predisposition to it. An increasing number of molecular markers identified by several research groups to diagnose patients with gastric cancer at an early stage and to screen the patients with a high risk of developing recurrence or metastases from those patients with a low risk[12‐17]. However, the fundamental molecular mechanism underlying tumorigenesis and tumor progression in gastric cancer is poorly understood and has not been fully elucidated. Thus, it is of great significance to identify effective indicators to better understand the biological basis for the survival of gastric cancer patients in order to provide important clinically relevant insights into disease management. In the current study, we demonstrated that the expression levels of PAK2 and pSer20PAK2 proteins were significantly higher in gastric cancer than in normal gastric mucosa. There were significant associations between PAK2, pSer20PAK2 expression and aggressive clinicopathological features. The overexpression of PAK2 and pSer20PAK2 proteins were both identified as independent prognostic factors in gastric cancer. These findings suggest that the activation of PAK2 may be a valuable diagnostic marker and therapeutic target for gastric cancer. To the best of our knowledge, this is the first report to determine the correlation between PAK2, pSer20PAK2 expression and clinical factors in gastric cancer.

The primary hallmark of cancer is the growth of tumor cells and the ability to form tumors[18]. PAKs were originally shown to be important for transformation in experiments where a kinase dead mutant of PAK was expressed in fibroblasts together with an oncogenic Ras mutant[19]. Subsequently, it has been demonstrated that PAKs are involved in stimulation of cell proliferation (including anchorage-independent growth), stimulation of cell survival (inhibition of apoptosis), and stimulation of cell motility, which are all the most prominent hallmarks of cancer[19]. Each of these three hallmarks has at least one known target in a well-established signaling pathway, which is a direct PAK target. In the PAK family, PAK2 is unique because it is not only activated by binding with the small G protein complex Cdc42/Rac, but it is also cleaved and activated by caspase-3 and similar proteases. After binding to Cdc42/Rac, the autoinhibitory activity of PAK2 is attenuated, leading to the autophosphorylation and activation of PAK2[20‐22]. Recent studies have established the function of PAK2 in cancer and identified it as an invasiveness-associated gene which is implicated with cancer proliferation and survival. For example, Li et al.[11] revealed that PAK2 was highly expressed in breast cancer cell lines and breast invasive ductal carcinoma tissue suggesting that highly expressed PAK2 might promote breast cancer progression and restrain the cell death response induced by chemotherapeutic drugs; Siu et al.[10] indicated that PAk2 and pPAK2 were both overexpressed in ovarian cancer cell lines and clinical samples of ovarian cancers compared with normal cell lines and benign ovarian lesions/inclusion cysts. They also found that knockdown of PAK2 in ovarian cancer cell lines reduced cell migration and invasion but did not affect cell proliferation and apoptosis, suggesting that PAK2 and pPAK2 may play important roles in ovarian carcinogenesis. In line with these previous findings, our data showed the upregulation of PAK2 and pSer20PAK2 in gastric cancer tissues, implying the activation of PAK2 in tumorigenesis of this disease. Then, our statistical analysis found that the overexpression of PAK2 and pSer20PAK2 proteins may be associated with higher tumor depth, greater extent of lymph node metastasis, positive distant metastasis and advanced tumor stage, suggesting that the activation of PAK2 may be involved in the aggressive tumor progression of gastric cancer. More interestingly, the aberrant expressions of PAK2 and pSer20PAK2 proteins were both independent prognostic factors for gastric cancer.

In conclusion, our data suggest for the first time that the activation of PAK2 may be associated with advanced tumor progression of gastric cancer. The overexpression of PAK2 and pSer20PAK2 proteins may be recognized as independent prognostic markers for overall survival, therefore, the detection of these proteins may be helpful for predicting clinical outcome for patients with gastric cancer.