Ann Surg Treat Res.  2014 Nov;87(5):232-238. 10.4174/astr.2014.87.5.232.

Comparison of putative circulating cancer stem cell detection between the hepatic portal system and peripheral blood in colorectal cancer patients

Affiliations
  • 1Department of Surgery, Pusan National University Yangsan Hospital, Yangsan, Korea. skm171@empas.com
  • 2Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Korea.
  • 3Department of Physiology, Pusan National University School of Medicine, Yangsan, Korea.
  • 4Department of Biochemistry, Pusan National University School of Medicine, Yangsan, Korea.
  • 5Department of Laboratory Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea.
  • 6Department of Pathology, Pusan National University Yangsan Hospital, Yangsan, Korea.

Abstract

PURPOSE
The present pilot study was conducted to detect putative cancer stem cell (CSC) from the hepatic portal system and peripheral blood in the colorectal cancer patients and to compare them to healthy donor and diverticulitis patients.
METHODS
Laboratory study was performed to identify the expression of cell surface markers, epithelial cell adhesion molecule (EpCAM), cytokeratin (CK) 18, CK20, CD44, and CD133, on several colon cancer cell lines. Clinical pilot study was conducted to detect putative circulating CSC as EpCAM+CD133+ cell in colorectal cancer (n = 10), diverticulitis (n = 5), and four healthy donors, by using flow cytometry. Blood was drawn from the hepatic portal system and peripheral vein.
RESULTS
On laboratory study, EpCAM was expressed in whole colon cancer cell lines, and CD44 and CD133 were simultaneously expressed in 50% of the cell lines with stemness phenotype, but CK18 and CK20 were not expressed in most of the cell lines. On clinical study, the mean EpCAM+CD133+ cell counts of 11.6/105 in the hepatic portal system were somewhat lower than 15.4/105 in peripheral vein (P = 0.241). As for diverticulitis patients, EpCAM+CD133+ cells were also detected to have steeper dropped to near zero, after the surgery.
CONCLUSION
The numbers of putative CSC were not statistically different between the detection sites of the portal vein and peripheral vein in the colon cancer patients. Therefore, we may not have benefitted by getting the cells from the hepatic portal system. In addition, the CD133+EpCAM+ cells in the colon cancer patients might contain normal stem cells from cancer inflammation similar to diverticulitis.

Keyword

Cancer stem cell; Hepatic portal system; Colorectal cancer; CD133; EpCAM

MeSH Terms

Cell Count
Cell Line
Colonic Neoplasms
Colorectal Neoplasms*
Diverticulitis
Epithelial Cells
Flow Cytometry
Humans
Inflammation
Keratins
Neoplastic Stem Cells*
Phenotype
Pilot Projects
Portal System*
Portal Vein
Stem Cells
Tissue Donors
Veins
Keratins

Figure

  • Fig. 1 EpCAM+CD133+ cell count according to the period of colorectal cancer patients (n = 10). EpCAM, epithelial cell adhesion molecule; PBMC, peripheral blood-derived mononuclear cell; POD, postoperative day.

  • Fig. 2 EpCAM+CD133+ cell count according to the period of diverticulitis patients (n = 5). EpCAM, epithelial cell adhesion molecule; PBMC, peripheral blood-derived mononuclear cell; POD, postoperative day.

  • Fig. 3 EpCAM+CD133+ cell count flows of colorectal cancer patients (n = 10) (The dotted line represents the mean value). EpCAM, epithelial cell adhesion molecule; PBMC, peripheral blood-derived mononuclear cell; POD, postoperative day.

  • Fig. 4 EpCAM+CD133+ cell count flows of diverticulitis patients (n = 5) (The dotted line represents the mean value). EpCAM, epithelial cell adhesion molecule; PBMC, peripheral blood-derived mononuclear cell; POD, postoperative day.


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