High expression of substance P and its receptor neurokinin-1 receptor in colorectal cancer is associated with tumor progression and prognosis
Received 11 December 2015
Accepted for publication 31 March 2016
Published 16 June 2016 Volume 2016:9 Pages 3595—3602
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 2
Editor who approved publication: Dr William Cho
Xiao-Yi Chen,1,* Guo-Qing Ru,2,* Ying-Yu Ma,1 Jun Xie,3 Wan-Yuan Chen,2 Hui-Ju Wang,1 Shi-Bing Wang,1 Li Li,1 Ke-Tao Jin,4 Xiang-Lei He,2 Xiao-Zhou Mou1
1Clinical Research Institute, 2Department of Pathology, Zhejiang Provincial People’s Hospital, Hangzhou, 3Department of Anus-Intestines, Affiliated Hospital of Shaoxing University, 4Department of Gastrointestinal Surgery, Shaoxing People’s Hospital, Shaoxing Hospital of Zhejiang University, Shaoxing, People’s Republic of China
*These authors contributed equally to this work
Background: Epidemiologic evidence suggests that chronic inflammation and/or chronic infection is associated with cancer development, and the inflammatory process may play a crucial role in the carcinogenesis and prognosis of colorectal cancer (CRC). Substance P (SP) belongs to the family of tachykinins and acts as an immunomodulator, binding to the neurokinin-1 receptor (NK1R) to initiate tumor cell proliferation, angiogenesis, and migration, steps that are critical for tumor cell invasion and metastasis. It is suggested that SP/NK1R signaling may play an important role in cancer progression and metastasis. However, the exact involvement and significance of SP and NK1R in CRC pathologies remain to be adequately deciphered.
Patients and methods: We performed immunohistochemistry staining on tissue microarrays containing 267 pairs of CRC and adjacent normal tissues to evaluate the clinical significance of SP or NK1R in the progression and prognosis of CRC. We also explored the potential correlation between SP and NK1R in CRC development.
Results: Expression levels of SP and NK1R were upregulated in CRC compared with their expressions in adjacent normal tissues (P<0.001). High expression of SP in CRC was significantly associated with lymph node metastasis (P<0.001). We also found that high expression of NK1R in CRC was significantly related to TNM (tumor node metastasis) stage (P=0.010) and lymph node metastasis (P=0.019). A high correlation between SP and NK1R expression was also observed (r=0.419, P<0.001). Survival analysis showed that CRC patients with high expression of SP or NK1R have a poor prognosis when compared to patients with low SP or NK1R expression (log rank test, P<0.05). Multivariate analysis using Cox regression model showed that survival was independently correlated with lymph node metastasis, distant metastasis, and SP expression (P<0.05).
Conclusion: Upregulation of SP-NK1R may play a crucial role in CRC progression. Moreover, SP-NK1R expression may also be used as a predictor for CRC prognosis.
Keywords: SP, NK1R, CRC, progression, prognosis
Colorectal cancer (CRC) is the fourth leading cause of cancer-related deaths in the world, with increasing mortality observed in recent years.1,2 In the People’s Republic of China, CRC is one of the eight most common forms of malignancy.3 Despite advances in clinical research and care, as well as knowledge regarding molecular mechanisms involved in CRC, relatively poor prognosis and high death rates are major challenges for CRC treatment. Moreover, the mechanisms associated with the pathogenesis of CRC are still not completely defined. Development of CRC is thought to begin with accumulated genetic changes in a cell such as point mutations, deletions and amplification, and methylation of DNA, leading to irreversible genetic damage.4 Recently, many studies have demonstrated that mediators of inflammation can induce DNA damage and lead to initiation and progression of cancer.5 Evidence also suggests that chronic inflammation and/or chronic infection is associated with cancer development in various types of tumor, including the development of CRC.5
Tachykinins include an evolutionary conserved family of peptide hormones that are potent immunomodulators and have been shown to have implications in the process of carcinogenesis. It is known that substance P (SP), neurokinin A (NKA), and neurokinin B (NKB) belong to the tachykinin family as proinflammatory neuropeptides.6,7 SP and NKA are derived from the preprotachykinin A gene, whereas NKB is derived from the preprotachykinin B gene. The biological actions of SP, NKA, and NKB are mediated by receptors named neurokinin-1 receptor (NK1R), neurokinin-2 receptor, and neurokinin-3 receptor. SP is synthesized by various cells, regulating biological processes such as exocrine and endocrine secretion, connective tissue proliferation, and blood pressure regulation.8,9 Most importantly, SP plays a role in regulating neurogenic inflammation and immune responses in peripheral tissues and the central nervous system.10,11 The receptor subtype NK1R has the highest activity for SP and has been identified in many cancer subtypes and can mediate various physiologic and pathophysiologic responses, including cell proliferation, migration, and inflammation.12–17 Studies have demonstrated that expression levels of functional NK1R in tumor are associated with the degree of malignancy of those tumors.16,18 Binding of SP to NK1R initiates tumor cell proliferation, angiogenesis, and migration, which are critical for tumor cell invasion and metastasis, implicating an important role of SP/NK1R signaling in cancer progression and metastasis.19–22 Researchers found that in tumor tissues the NK-induced signaling is altered when compared to normal cells so as to support proliferation and survival of cancer cells. Our previous study suggested that NK1R polymorphism alone or in combination with NK2R is a promising prognostic marker of lymph node metastasis in CRC patients.23 However, the exact signaling cascades involved and the role of SP and NK1R in CRC pathologies remain to be elucidated.
In order to pin the role of inflammatory processes in CRC, here, we evaluate the expression of SP and NK1R and its clinical significance in CRC patients to explore the potential association between SP and NK1R in CRC progression and prognosis. We expect that understanding the involvement of inflammatory processes in CRC, in combination with any other genetic factors, could be used as a tool to reduce the incidence of CRC and for better clinical management of the disease.
Patients and methods
The present study was approved by the Ethics Committee of Zhejiang Provincial People’s Hospital (Hangzhou, Zhejiang, China). All patients provided written informed consent. The expression levels of SP and NK1R were evaluated by immunohistochemical staining of tissue microarrays (TMAs) (Shanghai Biochip Co., Ltd., Shanghai, People’s Republic of China). The TMAs contain a total of 267 formalin-fixed, paraffin-embedded tumor samples from 267 CRC patients, while 267 adjacent normal tissues were derived as corresponding controls. All patients had follow-up records for >5 years, and the survival time was calculated from the date of surgery to the date of death or follow-up deadline.
TMA sections were then used for the immunohistochemical staining as described previously.24 Briefly, TMA sections were deparaffinized with xylene and then dehydrated through descending grades of ethanol to deionized water according to standard procedures. After antigen retrieval with the appropriate buffer (0.01 M citrate buffer, pH 6.0, high to boiling) for 3 minutes, the sections were cooled at room temperature. Endogenous peroxidase was blocked with 3% (v/v) aqueous hydrogen peroxide for 10 minutes, followed by incubation with normal serum for 20 minutes to reduce nonspecific binding. Then, the sections were incubated with a primary antibody against SP (1:100, SC9758; Santa Cruz Biotechnology Inc., Dallas, TX, USA) or an antibody against NK1R (1:250, SC14116; Santa Cruz Biotechnology Inc) overnight at 4°C. Negative controls were included, and steps were carried out with PBS. Subsequently, TMA sections were incubated with biotin-labeled secondary antibody (Thermo Fisher Scientific, Waltham, MA, USA) for 20 minutes at room temperature, followed by incubation with streptavidin-biotinylated horseradish peroxidase-conjugated antibody (Thermo Fisher Scientific) for another 20 minutes. Finally, the sections were stained with 3,3-diaminobenzidine and lightly counterstained with Mayer’s hematoxylin, dehydrated, and mounted with resinous mounting medium.
Evaluation of immunohistochemical staining
The degree of immunostaining was examined semiquantitatively and scored under a light microscope by two independent expert pathologists without prior knowledge of the clinical data. Expression level of SP and NK1R was based on the Allred 8-unit system using the combination of an intensity staining score and a proportion score of stained tumor cells. The staining intensity was scored as follows: 0 (no staining), 1 (weak staining, light yellow), 2 (moderate staining, yellow brown), and 3 (strong staining, brown). Proportion of stained tumor cells was scored according to the proportion of positively staining tumor cells: 0 for <5% positive tumor cells; 1 for 6%–25% positive tumor cells; 2 for 26%–50% positive tumor cells; and 3 for >51% positive tumor cells. For final evaluation, a total score of ≤4 was regarded as low expression for SP or NK1R, and a score of >5 was used to define tumors with high expression of SP or NK1R.
All statistical analyses were performed using the SPSS (Version 13.0; SPSS Inc., Chicago, IL, USA). To evaluate the associations between the expression of SP and NK1R and the clinicopathological features of the CRC patients, chi-square (χ2) test or Fisher’s exact test was used. Univariate survival analysis was performed using the Kaplan–Meier method accompanying log rank test. Cox proportional hazards regression model was used to perform multivariate survival analysis to estimate the predictors related to prognosis. Correlation between SP, NK1R protein expression, and clinicopathological parameters was estimated using Spearman correlation method. All P-values were two sided, and a P-value <0.05 was considered statistically significant.
Expression of SP and NK1R in CRC and adjacent normal tissues
The immunostaining for SP was predominant in the cytoplasm (Figure 1). SP was highly expressed in 183 (68.5%) of the 267 patients with CRC, which was significantly higher than the expression observed in the adjacent normal tissues (2.2%, 6/267, P<0.001). The immunostaining for NK1R was also mainly located in the cytoplasm. High expression levels of NK1R were detected in 199 (74.5%) of the 267 patients with CRC, significantly higher than that in the adjacent normal tissues (5.6%, 15/267, P<0.001). The scoring of immunohistochemical staining for SP and NK1R is shown in Figure 2.
Figure 2 The scoring of immunohistochemical staining for SP (A) and NK1R (B).
Patient characteristics and association of SP and NK1R expression with clinicopathological features of CRC
The patient cohort consisted of 142 males and 125 females, with a median age of 67 years (range 24–91) at the time of surgery. High expression of SP in CRC has no significant association with age, sex, distance metastasis, pathology grading, and TNM (tumor node metastasis) stage but was significantly associated with lymph node metastasis (Table 1). In all, 84.9% (90/106) of CRC patients with lymph node metastasis were detected with high expression of SP, which was higher than that without lymph node metastasis (57.8%, 93/161, χ2=21.837, P<0.001). The Spearman correlation coefficient of high SP expression with lymph node metastasis was 0.286 (P<0.001).
Table 1 Relationship of SP expression with clinicopathological features of CRC
High NK1R expression in CRC had no significant association with age, sex, distance metastasis, and pathology grading but was significantly related to lymph node metastasis and TNM stage (Table 2). High NK1R expression was detected in 83.0% (88/106) of CRC cases with lymph node metastasis, which was significantly higher than the expression in patients without lymph node metastasis (68.9%, 111/161, χ2=6.671, P=0.010). High NK1R expression was detected in 77.2% (176/228) of CRC patients with TNM stage III + IV, which was higher than the expression in patients with TNM stage I + II (59.0%, 23/39, χ2=5.823, P=0.019). The Spearman correlation coefficients of high NK1R expression with lymph node metastasis and TNM stage were 0.158 and 0.148 (P<0.05), respectively.
Table 2 Relationship of NK1R expression with clinicopathological features of CRC
Correlation of SP and NK1R expression with prognosis
Kaplan–Meier survival analysis showed that the 3- and 5-year cumulative survival rates for patients with high expression of SP were 43.8% and 22.8%, while for those with low SP expression, the survival rates were 82.5% and 75.0%, respectively (Figure 3). The follow-up time for the patients was in August 2013. The mean survival time for CRC patients with high SP expression was 43.53±2.42 months, and the survival time for patients with low SP expression was 79.98±1.60 months. Clearly, CRC patients with high expression levels of SP have a poorer prognosis (log rank test, χ2=68.010, P<0.001). The 3- and 5-year cumulative survival rates for patients with high expression of NK1R were 51.6% and 31.9%, while for those with a low NK1R expression, the survival rates were 65.5% and 56.4%, respectively. The mean survival time for CRC patients with high NK1R expression was 52.85±2.41 months and that for patients with low NK1R expression was 70.38±3.47 months. CRC patients with high expression of NK1R have a poorer prognosis (log rank test, χ2=11.333, P=0.001). Multivariate analysis using Cox regression model showed that survival rate was independently correlated with lymph node metastasis, distance metastasis, and SP expression (P<0.05; Table 3).
Figure 3 Kaplan–Meier survival analysis for CRC patients with SP (A) and NK1R (B) expression.
Table 3 Cox regression analysis of the clinicopathological parameters in colon cancer patients
Association between SP and NK1R expression levels in CRC
Our results indicate a high correlation between SP and NK1R expression in CRC. Of the 183 patients with high expression of SP, 155 (84.7%) also had a high expression of NK1R. The correlation between the expression of SP and NK1R in patients with CRC was statistically significant (r=0.419, P<0.001, Spearman’s ρ-test).
Links between cancer and inflammation were made on the basis of observations that the tumors often arose at the sites of chronic inflammation and the presence of inflammatory cells in the biopsy samples from tumor.5 It is widely accepted that the inflammation mediators and cellular effectors are important constituents of tumor microenvironments.25 Recently, the effects of the inflammatory response on the development of neoplasia were demonstrated in various types of cancers such as breast, endometrial, ovarian, and colon tumors.5 It has been observed that patients with inflammatory bowel diseases are at an increased risk of neoplasia development and progression to CRC. Inflammation is considered to be an important risk factor for the development of CRC.26
SP is secreted by nerve fibers and inflammatory cells such as macrophages, lymphocytes, and eosinophils and has a proinflammatory effect and participates in inflammatory immune responses. The link between inflammation and cancer could be explained through SP-centered models.20 Numerous studies have reported the involvement of the SP/NK1R system in cancer.27 SP can induce mitosis in normal and tumor cells and protects tumor cells from apoptosis.21,28,29 Binding of SP to NK1R triggers the release of secondary messengers (cAMP) triggering a number of effector mechanisms involved in the regulation of cellular functions.30 It has previously been reported that NK1R activation can induce the phosphorylation of Akt and MAPK family members, which subsequently lead to the activation of different transcription factors regulating the expression of respective target genes.30–34 The regulatory mechanisms stimulate DNA synthesis and/or cytokine secretion and mediate the antiapoptotic effect.35 However, the function of SP-NK1R pathway in the regulation of inflammation-induced pathogenesis in CRC is poorly understood.
In this study, we evaluated the expression levels of SP and NK1R in CRC and showed that the expression levels can be implicated in the prediction of CRC prognosis. SP expression was upregulated in CRC as compared with that in adjacent normal tissues, and elevated SP expression was significantly associated with lymph node metastasis. This result is consistent with the findings associating the role of SP in the migration of tumor cells leading to metastasis, which is a major problem in the treatment of tumors. Moreover, it has been recently reported that the cerebral metastases result from SP-mediated process.36 Our results indicate that SP is a proinflammatory modulator, and its expression levels are linked to different stages of CRC development.
It is well known that malignant tissues have high expression levels of NK1R, and a large percentage of malignant tumor cell phenotypes show increased NK1R expression.37 Similarly, we found that the expression of NK1R was upregulated in CRC as compared with that in adjacent normal tissues, and elevated expression was significantly associated with lymph node metastasis and TNM stage. Besides, our results showed that patients with high expression of SP also had a high rate of upregulated expression of NK1R in CRC. Our results strongly indicate that SP/NK1R system can be used as a mark predicting the invasion and metastasis of CRC. The results also indicate the involvement of inflammatory processes in the tumor microenvironment.
A strong tumor-associated inflammatory reaction analogous to a wound-healing response can be initiated by cancer therapy.38 The outcome of therapy-induced inflammatory response can have tumor-promoting functions similar to necrosis, which accompanies rapid tumor growth.39,40 As a result, the inflammation may also play an important role in the prognosis of CRC. Turner et al41 examined the relationship between tachykinin concentrations and survival of tumor patients and indicated that tachykinins in tumor patients could be used as a strong prognostic indicator. Our study also shows that CRC patients with high expression of SP or NK1R have a poor prognosis. However, one of the drawbacks of our study is the use of TMA, where the amount of tissue analyzed using this technique is limited and may not be representative of the whole specimen. This may pose a significant problem in malignant epithelial tumors where there is a high degree of intratumoral heterogeneity. Therefore, further analysis about the association between SP or NK1R and CRC development is still to be studied.
Upregulated expression of SP-NK1R may play a crucial role in CRC progression; moreover, SP-NK1R expression may also be used as a predictor for prognosis of CRC. Based on these findings, regulation of SP and NK1R expression and/or the inhibition of the potential signaling pathways associated with SP and NK1R could be used to develop novel therapeutic strategies for CRC in the future.
This work was supported by the National Science Foundation of China (nos 81201783, 81372463, and 81472210), Zhejiang Provincial Natural Science Foundation of China (nos LY15H160051, LY14H160041, and LY13H080005), Funds of Science Technology Department of Zhejiang Province (no 2014C37101), Zhejiang Province Bureau of Health (no 2015ZA009), and Open Fund of Zhejiang Provincial Top Key Discipline of Biology.
The authors report no conflicts of interest in this work.
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