This work was designed to study the clinical relevance of serum VEGF and IL-6 in patients with CRC.

The results of patient’s characteristics showed that CRC patients with metastasis had significantly higher percentage of abdominal discomfort, ESR (P = 0.02, and 0.005, respectively) than CRC patients with localized lesions [Table 1]. Patients with advanced clinical stages had significantly higher levels of VEGF and IL-6 than those with early clinical stage (P < 0.001) [Table 2].

CRC patients with or without metastasis had significantly higher VEGF and IL-6 levels than controls (all P ≤ 0.001). Patients with metastatic disease had significantly higher VEGF and IL-6 levels than those with localized disease (P< 0.001) [Table 3].

Using cutoff values 240 pg/ml for VEGF and 6.7 pg/ml for IL-6, the diagnostic accuracy for invasiveness was found to be 83% and 66% respectively, with sensitivity 79% and 74% and specificity 68% and 59%, respectively [Table 4].

CRC patients had higher VEGF levels than healthy controls. Also, significantly higher serum VEGF was found in CRC patients with advanced clinical stages than in those with an early clinical stage, and in patients with metastasis than those with localized cancer. These findings run in parallel with previous reports where, the metastatic colon cancer expressed significantly more VEGF gene than localized tumors.[^{8, 17}] The occasional discrepancies in the results of the different studies could be explained by certain factors, e.g. inflammation, tumor infiltrating cells, and number of platelets in the serum sample.[¹⁸] Patients with high serum VEGF had high pathological tumor stage and regional lymph node metastasis. VEGF could modulate lymph vessel density and microvessel density that correlate with the malignant potential of tumors, patient survival and could be a useful tool for the selection of postoperative management and treatment strategies in patients with CRC.[¹⁹] Therefore, high serum VEGF could be considered as an usher for advanced disease state and tumor metastasis in CRC patients. Similar to the findings of Ueda et al., who reported that an increase in the serum level of VEGF was shown to be a predictor of metastasis in gastrointestinal tumors.[²⁰]

There is a dynamic relationship among tumor cells, inflammatory cells, cytokines, and chemokines.[²¹] Cytokines and chemokines within tumors can contribute to the progression of tumors to a more aggressive metastatic phenotype or play a role in tumor therapy.[^{17, 22}] IL-6 is most often classified as a proinflammatory cytokine, although IL-6 and IL-6 -regulated acute phase proteins were previously suggested as anti-inflammatory and immunosuppressive, and may negatively regulate the acute -phase response.²³

Our results proved higher levels of IL-6 in patients with CRC than healthy controls. Similarly, higher levels of IL-6 were found in metastatic than non -metastatic CRC patients. Our results are in agreement with the previous studies that reported increased circulating levels of IL-6 in patients with advanced pathological stages of CRC.[¹⁰] Previous correlation between tumor tissue expression of IL-6 and serum concentration in CRC implies that increased systemic IL-6 might be a result of local tumor production.[²⁴] These findings have encouraged us to suggest the possible role of IL-6 as a trigger for the disseminated cells to develop into metastatic tumors. We ask for more clinical trials addressing the investigation of the novel genetic and pharmacologic agents including anti -angiogenic agents giving hope for future therapies which could be suitable for advanced CRC patients.

IL-6 can be released from tumor infiltrating leukocytes,[²⁵] but is produced to a large extent by tumor cells themselves. In human colon cancer, IL-6 expression parallels tumor progression, reaching a maximum in high grade cancerous lesions.[⁹] In addition, IL-6 increases invasiveness of colon cancer cells and likely promotes secondary tumor formation through its angiogenic potency. The role of IL-6 in promoting progression and metastatic spread of colon cancer depends not only on the extent of basal but also, importantly, on the extent of inducible IL-6 expression at certain stages of tumor development.[¹⁰] Thus, IL-6 could serve as autocrine and paracrine growth factor for CRC, and high serum level of this cytokine might correlate with the poor prognosis and the increased production of angiogenic factors.

IL-6 has been shown to correlate with platelet count and platelet VEGF content. As circulating VEGF is mostly transported by platelet, IL-6 could be regarded as an indirect angiogenic factor that facilitates the production and distribution of VEGF to the metastatic sites. The importance of IL-6 on VEGF metabolism has been confirmed.[⁴] Both VEGF and IL-6 possibly have a role in stimulation of CRC growth and metastasis. An association between VEGF and IL-6 has been previously reported in carcinomas of the breast.[²⁶] Although the biological mechanisms linking metastatic CRC with the increase in the serum levels of IL-6 and VEGF are not clearly understood, the findings of this study support a possible link between the advanced clinical disease and these cytokines.

In conclusion, in the CRC patients, raised serum VEGF and IL-6 may prove valuable non-invasive diagnostic indicators associated with advanced clinical stage and tumor metastasis that warrants further investigations.

Source of Support: Nil

Conflict of Interest: None declared.