Abstract

BackgroundThe presence of peripheral circulating tumor cells indicates the possible existence of a tumor in vivo; however, low numbers of circulating tumor cells (CTCs) can be detected in peripheral blood of healthy individuals as well as patients with benign tumors. It is not known whether peripheral CTC counts differ between patients with benign colorectal disease and those with colorectal cancer.MethodsComparative analysis of preoperative peripheral circulating tumor cells counts was completed in patients with benign colorectal disease (colorectal polyps) and non-metastatic cancer of the colon and rectum.ResultsThe results of this analysis showed that patients with colorectal cancer had higher CTC counts than patients with colorectal polyps (3.47 ± 0.32/3.2 ml vs 1.49 ± 0.2/3.2 ml, P < 0.001). Colorectal cancer patients with tumors of the sigmoid colon displayed the highest CTC counts (4.87 ± 0.95/3.2 ml), followed by those with tumors of the rectum (3.73 ± 0.54/3.2 ml), ascending colon (3.5 ± 0.63/3.2 ml), transverse colon (2.4 ± 0.68/3.2 ml), and descending colon (2.08 ± 0.46/3.2 ml). Colorectal polyp patients with polyps in the rectum showed the highest CTC counts (2.2 ± 0.77/3.2 ml), followed by those with polyps in the ascending colon (1.82 ± 0.54/3.2 ml), sigmoid colon (1.38 ± 0.25/3.2 ml), transverse colon (0.75 ± 0.25/3.2 ml), and descending colon (0.33 ± 0.21/3.2 ml). The differences in CTC counts suggest that anatomical location of colorectal tumors may affect blood vessel metastasis. Meanwhile, patients with moderately differentiated and poorly differentiated tumors displayed higher peripheral blood CTC counts compared to those with well-differentiated tumors (P < 0.001). This result suggests that the type of tissue differentiation of colorectal tumors may act as another factor that affects blood vessel metastasis.ConclusionsCirculating tumor cells can be detected in the peripheral blood of colorectal cancer patients as well as patients with colorectal polyps. The differences in CTC counts suggest that anatomical location and the type of tissue differentiation of colorectal tumors may affect blood vessel metastasis.

Highlights

  • The presence of peripheral circulating tumor cells indicates the possible existence of a tumor in vivo; low numbers of circulating tumor cells (CTCs) can be detected in peripheral blood of healthy individuals as well as patients with benign tumors

  • Tissue differentiation of colonic and rectal polyps was primarily classified as high-grade intraepithelial neoplasia (72.13%), whereas tissue differentiation of colonic and rectal carcinoma was mainly classified as moderately differentiated adenocarcinoma (69.72%)

  • Comparison of CTC counts between colorectal polyps and colorectal carcinoma According to previous reports [14] and the CTC counts in Table 1, CTC counts were divided into two groups: > 1/3.2 ml and ≤ 1/3.2 ml

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Summary

Introduction

The presence of peripheral circulating tumor cells indicates the possible existence of a tumor in vivo; low numbers of circulating tumor cells (CTCs) can be detected in peripheral blood of healthy individuals as well as patients with benign tumors. Further studies are required to determine whether peripheral CTCs are differentially expressed in benign colorectal disease and non-metastatic colorectal cancer and whether detection of CTCs accurately reflects the pathological characteristics of the primary tumor in benign and malignant colorectal diseases To address these questions, we completed a comparative analysis of peripheral CTC counts in patients with colorectal polyps and colorectal cancer

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