Abstract
Objective
Hyperuricemia is linked to the prognosis of a number of cancers; however, its association with colon cancer survival has not been fully elucidated. To investigate whether hyperuricemia affects the prognosis of colon cancer, we conducted a retrospective study.
Methods
The study included age- and sex-matched colon cancer patients, of whom 60 patients were diagnosed with hyperuricemia, and 120 patients did not have hyperuricemia. The overall survival (OS) and disease-free survival (DFS) of these patients were evaluated by Kaplan–Meier (K-M) analysis. The association between the survival of colon cancer patients and hyperuricemia was analyzed using the Cox regression method after adjusting for tumor stage and grade and vascular infiltration.
Results
The K-M survival analysis supported that patients with hyperuricemia had poor OS (P for the Log rank test = 0.0008) and DFS. As demonstrated by the univariate analysis, the presence of hyperuricemia was correlated with decreased OS (HROS = 2.09, P = 0.002). Tumor grade and tumor stage were also found to be independent predictors for the prognosis of colon cancer patients. In addition, poor OS among patients with hyperuricemia was also confirmed in the adjusted analysis (HROS = 1.94, P = 0.005).
Conclusion
Hyperuricemia has an adverse effect on the prognosis and survival of patients with colon cancer. Further studies evaluating the cellular and molecular mechanisms are needed to validate the prognostic value of hyperuricemia in colon cancer.
Keywords: colon cancer, hyperuricemia, survival, prognosis, uric acid, biomarker
Introduction
Colon cancer poses a major threat to public health and is the leading cause of cancer-related death worldwide.1 Although there has been progress in colon cancer diagnosis, patients with colon cancer still have a low survival rate, especially patients at an advanced stage.2,3 The discovery of factors associated with cancer prognosis might help develop therapies with higher efficiency and improve the prognosis of colorectal cancer patients. Many studies have suggested that metabolism-related factors exert vital effects on the prognosis of colon cancer. Previous studies have shown that colorectal cancer patients with diabetes mellitus have a higher mortality risk and lower disease-free survival rate than those without diabetes mellitus.4 Xiao et al confirmed that Exo70 was an independent prognostic factor in colon cancer.5 And Ren et al found high expression of PLAC1 was related to poor prognosis of colon cancer patients.6 In the last decade, the correlation between hyperuricemia and the incidence and mortality in multiple cancers has drawn much attention.
Uric acid, found in serum, is a molecule possessing antioxidant and pro-oxidant properties.7,8 Hyperuricemia is characterized by elevated levels of uric acid in the serum, which enhances the local or systemic inflammatory response.9 Abnormal metabolism of serum uric acid may cause cardiovascular disease, respiratory disorders, renal disease and metabolic syndrome.10,11 Interestingly, uric acid may prevent cancer due to its antioxidant properties regardless of its pro-inflammatory effect.10–12 Conversely, a high level of uric acid present in the serum is independently correlated with increased mortality in cancer.13 However, the effect of hyperuricemia on the survival rate of colorectal cancer patients remains unclear. Here, we investigated the impact of hyperuricemia on the prognosis of colon cancer patients.
Materials and Methods
Research Design
Patients with histologically diagnosed colon cancer (from July 2002 to June 2014) at our hospital were recruited in this retrospective cohort study. A total of 180 colon cancer patients, including 60 patients with hyperuricemia and 120 patients without hyperuricemia matched by age, gender, tumor location, and treatment methods, and so on. The study was conducted following approval from the local human research ethics committee. Informed consent forms were signed by all participants. All patients have strictly followed the treatment protocol in our hospital, which is comparable between the two groups. Patients were excluded if they had a previous history of diabetes mellitus, coronary artery disease, cerebrovascular diseases, or treatment for hyperuricemia or if they had no information on the levels of uric acid or were not followed up. We recorded the age, sex and race of patients, the date and time of diagnosis, the stage, size and grade of tumors, vascular infiltration, and level of serum uric acid. TNM staging system was adopted in the diagnosis of colorectal cancer, which was divided into I, II, III and IV stages according to the depth of primary tumor invasion, regional lymph node metastasis and distant metastasis. According to the College of American Pathologists and World Health Organization, grade is assessed by calculating the percentage of gland forming in the tumor. Low-grade tumors have over 50% gland forming (well or moderately differentiated) and high-grade tumors have less than 50% gland forming (poorly differentiated).14 Vascular infiltration was defined as tumor within a round or ovoid vessel-like structure containing elastic tissue fibers arranged in an orderly concentric fashion including intramural and extramural blood vessel invasion.15
Uric Acid Assay
Prior to therapy, blood samples were collected by a single peripheral venous puncture. The level of serum uric acid was determined using the EDTA hydrazine method. Patients with serum uric acid levels greater than 420 µmol/L (male) or 360 µmol/L (female) were diagnosed with hyperuricemia.
Outcome Estimation
We investigated the correlation of hyperuricemia with the overall survival (OS) and disease-free survival (DFS) of colon cancer patients. Patients included in this study were followed-up quarterly for three years and then half-yearly. All patients receives follow-up till to death or the end of follow-up or loss of visit. The most recent follow-up record in this study was performed on May 20, 2019.
Statistical Analysis
The Kaplan–Meier method and the Log rank test were used to study the correlation of hyperuricemia with the OS of colon cancer patients. The hazard ratio (HR) with 95% confidence interval (CI) was determined, and Cox regression analysis was also performed. Covariates consisted of age (≥ 59 vs < 59), sex (male vs female), tumor grade (low vs high), TNM stage (III/IV vs I/II), and vascular infiltration (Yes vs No). STATA (version 12.0) was used for estimation.
Results
Table 1 summarizes the characteristics of all colon cancer patients. Patients with hyperuricemia had tumor stages and grades and vascular infiltration results that were similar to those in patients without hyperuricemia. However, colon cancer patients with hyperuricemia had significantly shorter OS and DFS than those without hyperuricemia, as revealed by the Kaplan–Meier analysis (Figures 1 and 2). In addition, the univariate analysis revealed that hyperuricemia was correlated with a decreased OS rate in colon cancer patients (HROS=2.09, 95% CI 1.32–3.31; P = 0.002) (Table 2). Furthermore, the multivariate analysis showed that hyperuricemia remained correlated with poor OS in colon cancer patients after adjustment for factors including age, sex, tumor stage and grade, and vascular infiltration (HROS=1.94, 95% CI 1.22–3.09; P = 0.005) (Table 2). The sensitivity analysis also strongly supported the findings mentioned above (data not shown), and the overall data remains stable and unaffected. In addition, colon cancer patients with low-grade tumors and tumors of advanced TNM stage had poor prognosis (Table 2).Accordingly, hyperuricemia was independently associated with poor prognosis of colon cancer.
Table 1.
Characteristics of Colon Cancer Patients
| Factors | Hyperuricemia (60) | Normouricemia (120) | P |
|---|---|---|---|
| Age, n (%) | 0.670 | ||
| <59 y | 36 (60.0%) | 68 (59.4%) | |
| ≥59 y | 24 (40.0%) | 52 (40.6%) | |
| Sex, n (%) | 0.600 | ||
| Female | 25 (41.7%) | 55 (45.3%) | |
| Male | 35 (58.3%) | 65 (54.7%) | |
| TNM stage, n (%) | 0.768 | ||
| I | 11 (18.3%) | 20 (16.6%) | |
| II | 10 (16.7%) | 24 (20.0%) | |
| III | 29 (48.3%) | 62 (51.7%) | |
| IV | 10 (16.7%) | 14 (11.7%) | |
| Tumor grade, n (%) | 0.483 | ||
| High | 41 (68.3%) | 88 (73.3%) | |
| Low | 19 (31.7%) | 32 (26.7%) | |
| Vascular infiltration, n (%) | 0.764 | ||
| Yes | 8 (13.3%) | 18 (15.0%) | |
| No | 52 (86.7%) | 102 (85.0%) | |
Figure 1.
Kaplan–Meier overall survival (OS) analysis (P for the Log rank test equal to 0.0008).
Figure 2.
Disease-free survival (DFS) analysis.
Table 2.
Cox Regression Analysis
| Univariate Analysis | Multivariate Analysis | |||
|---|---|---|---|---|
| HR (95% CI) | P | HR (95% CI) | P | |
| Age (≥59 years) | 1.40 (0.89–2.20) | 0.149 | 1.30 (0.82–2.07) | 0.268 |
| Sex (male/female) | 1.14 (0.72–1.80) | 0.582 | 1.13 (0.71–1.80) | 0.597 |
| Stage (III/IV) | 2.50 (1.44–4.34) | 0.001 | 3.30 (1.80–6.05) | <0.001 |
| Vascular infiltration | 0.72 (0.31–1.65) | 0.437 | 1.02 (0.42–2.47) | 0.970 |
| Tumor grade (low) | 1.36 (0.85–2.17) | 0.202 | 2.07 (1.25–3.44) | 0.005 |
| Hyperuricemia (with/without) | 2.09 (1.32–3.31) | 0.002 | 1.94 (1.22–3.09) | 0.005 |
Abbreviation: HR, hazard ratio.
Discussion
Chemotherapy is the optimal treatment for colon cancer patients after surgery and those with advanced colon cancer. At present, researchers are still searching for prognostic biomarkers that can indicate the efficacy of chemotherapy for colon cancer patients. The development of optimized chemotherapy and personalized treatments for colon cancer will benefit from the identification of prognostic factors for tumor progression.16,17 In particular, currently available data reveal that metabolic disorders of serum uric acid promote the development and progression of malignant tumors.18,19 However, the role of serum uric acid in colon cancer prognosis remains largely unknown. In this retrospective cohort study, we investigated whether hyperuricemia affected the prognosis of colon cancer. Overall, patients suffering from both colon cancer and hyperuricemia had a poor prognosis compared to colon cancer patients without hyperuricemia, regardless of age, sex, TNM stage, tumor grade, and vascular infiltration.
Studies have shown that high levels of serum uric acid can promote inflammation, resulting in hyperuricemia, gout and cardiovascular complications.20–22 Increased proliferation of tumor cells may contribute to elevated levels of serum uric acid, leading to hyperuricemia, suggesting a potential link between tumors and uric acid metabolism.23 However, the role of serum uric acid in carcinogenesis remains obscure due to its antioxidant and pro-inflammatory properties.12 Owing to its antioxidant properties, serum uric acid can reduce oxidation-induced cell damage. A number of studies have shown that hyperuricemia is also correlated with an increased risk of cancer.24,25 Furthermore, an increased level of serum uric acid is related to cancer outcomes, possibly reflecting more serious prognostic indications.24,25 Increased lysis of malignant cells can lead to hyperuricemia, which thus predisposes patients to an increased risk of renal failure and coronary heart disease.26,27 And Kalemkerian et al confirmed that renal insufficiency, elevated serum lactate dehydrogenase (LDH), and hyperuricemia were found in tumor lysis syndrome of solid tumors including colon cancer, which implied that tumor lysis syndrome is an important cause of hyperuricemia.28 Therefore, more data are needed to better interpret the underlying link between hyperuricemia and cancer.
Previous studies have suggested that hyperuricemia is correlated with the prognosis of several cancers. Tanriverdi et al found that non-small-cell lung cancer patients with hyperuricemia had a higher risk of tumor metastasis to the brain and poorer prognosis than patients without hyperuricemia.29 A recent study showed that hyperuricemia negatively impacts the prognosis of patients with osteosarcoma.30 However, increased levels of uric acid are correlated with improved clinical outcomes in patients diagnosed with soft-tissue sarcoma.31 We found that colon cancer patients with hyperuricemia had poor OS and DFS compared with those without hyperuricemia. Given that uric acid has diverse biological activities at different sites, such as serum, soft tissues and joints, an increase in uric acid from different origins might have varying effects on the development of tumors. Therefore, more studies are required to estimate the prognostic roles of uric acid in different malignant tumors.
The findings from this study must be interpreted cautiously due to the limitations of the cohort. The study was based on a retrospective design and employed a relatively small cohort to estimate cancer prognosis. In addition, different levels of serum uric acid might have different effects on the prognosis of patients with colon cancer. Future studies are encouraged to determine the precise prognostic role of different serum levels of uric acid in patients with colon cancer. Moreover, colon cancer patients with hyperuricemia receiving treatments and other comorbidities were excluded in this study, which might cause selection bias.
Conclusion
This study strongly suggests that hyperuricemia confers adverse effects on the prognosis of patients with colon cancer. Future studies are warranted to confirm the prognostic role of hyperuricemia, particularly regarding different levels of uric acid in the serum.
Acknowledgments
We are particularly grateful to all the people who have given us help on our article.
Funding Statement
There is no funding to report.
Ethics Approval and Consent to Participate
All patients in this research were informed of this study and signed consent forms. The study was approved by the ethics committee of Liyang People’s Hospital. All studies were conducted in accordance with the Declaration of Helsinki. There were no unethical experiments performed in this study. And the ethical approval number is 2020042.
Disclosure
The authors declare that they have no competing interests.
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