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Isolation of Human Endothelial Cells from Normal Colon and Colorectal Carcinoma - An Improved Protocol
Published on: April 4, 2018
Minimally invasive colorectal resection for cancer is associated with a short-lived decrease in soluble Tie-2
H M C Shantha Kumara1, Michael J Grieco, Xiaohong Yan
1Division of Colon and Rectal Surgery, Department of Surgery, St. Luke's-Roosevelt Hospital Center, Suite 7B, 425 West 59th Street, New York, NY 10019, USA. hmsach_6@yahoo.com
Background:
Angiopoetin- (Ang-) 1 inhibits and Ang-2 promotes VEGF-mediated angiogenesis via binding to endothelial cell-bound Tie-2 receptor (Tie-2). After minimally invasive colorectal resection (MICR), Ang-1 levels decrease and Ang-2 levels increase, which may stimulate angiogenesis in wounds and residual tumor foci. Soluble Tie-2 (sTie-2) modulates the effects of free Ang-1 and Ang-2 by binding to them. This study assessed perioperative MICR plasma sTie-2 levels.
Methods:
Blood samples were taken preoperatively (PreOp) and on postoperative days (POD) 1 and 3 from 50 cancer and 53 benign disease MICR patients. In a subgroup, a fourth sample was taken between POD7 and POD13 and bundled as a single time point. sTie-2 levels (ng/ml) were determined via ELISA. The mean and SD were determined at each time point. The t test used for analysis.
Results:
PreOp plasma sTie-2 levels were significantly higher in the benign group (27.6 ± 10.2) than in the cancer group (22.9 ± 7.9). A significant drop from PreOp occurred in sTie-2 levels in the cancer group on POD1 (20.0 ± 7.4) and POD3 (21.0 ± 6.6) and in the benign group on POD1 (24.8 ± 9.1). The benign group's POD3 and the cancer group's POD7-13 sTie-2 levels were statistically similar to the PreOp levels while the benign group's POD7-13 level was significantly higher.
Conclusion:
PreOp sTie-2 levels were significantly lower in cancer patients. MICR is associated with a significant short-lived decrease in plasma sTie-2 levels in cancer patients on POD1 and 3, which may briefly inhibit VEGF-mediated angiogenesis. The benign group's early results were similar.
Insights
Preoperative plasma soluble Tie-2 (sTie-2) levels were lower in cancer patients undergoing minimally invasive colorectal resection (MICR). Postoperative levels decreased significantly in cancer patients, potentially inhibiting angiogenesis.
Area of Science:
- Vascular biology
- Oncology
- Surgical research
Background:
- Angiopoietin-1 (Ang-1) inhibits and Angiopoietin-2 (Ang-2) promotes VEGF-mediated angiogenesis via Tie-2 receptor binding.
- Minimally invasive colorectal resection (MICR) alters Ang-1 and Ang-2 levels, potentially influencing angiogenesis in surgical sites and tumors.
- Soluble Tie-2 (sTie-2) acts as a decoy receptor, modulating Ang-1 and Ang-2 activity.
Purpose of the Study:
- To assess perioperative plasma levels of soluble Tie-2 (sTie-2) in patients undergoing MICR.
- To compare sTie-2 levels between cancer and benign disease patients.
- To investigate the dynamic changes in sTie-2 levels during the perioperative period.
Main Methods:
- Blood samples collected preoperatively (PreOp) and on postoperative days (POD) 1 and 3 from 50 cancer and 53 benign disease MICR patients.
- A subgroup had a fourth sample taken between POD7 and POD13.
- Plasma sTie-2 levels were quantified using ELISA, with statistical analysis performed using the t-test.
Main Results:
- PreOp sTie-2 levels were significantly lower in the cancer group (22.9 ± 7.9 ng/ml) compared to the benign group (27.6 ± 10.2 ng/ml).
- A significant drop in sTie-2 levels was observed on POD1 and POD3 in the cancer group, and on POD1 in the benign group.
- sTie-2 levels in the benign group on POD7-13 were significantly higher than PreOp levels, while cancer group levels on POD7-13 were similar to PreOp.
Conclusions:
- Preoperative sTie-2 levels are significantly lower in cancer patients undergoing MICR.
- MICR is associated with a transient, significant decrease in plasma sTie-2 levels in cancer patients on POD1 and 3.
- This short-lived reduction in sTie-2 may temporarily inhibit VEGF-mediated angiogenesis following colorectal resection.

