38. Influence of different CO2 pneumoperitoneum pressures on the expression of adhesion molecules on gastric cancer cells
Original Article

38. Influence of different CO2 pneumoperitoneum pressures on the expression of adhesion molecules on gastric cancer cells

Yan Shi, Pei-Wu Yu, Feng Qian, Xiao Lei, Hua-Xing Luo, Yong-Liang Zhao, Bo Tang, Ying-Xue Hao, Peng Yin, Jing Li

Department of General Surgery and Center of Microinvasive Gastrointestinal Surgery, Southwest Hospital, Third Military Medical University, Chongqing 400038, China


Objective: To study the effect of different carbon dioxide pneumoperitoneum pressures on the expression of adhesion molecules on human gastric cancer cells line MNK-45.
Methods: MKN-45 in experimental groups were exposed to simulated CO2 environment maintained at different pressures (9, 12, 15 mmHg) for 4 hours. Control groups were exposed to room air At the 0, 24, 48, 72, 96 hours after treatment, CD44v6, ICAM- 1 and E-cadherin were detected by flow cytometry method.
Results: CD44V6 and ICAM-1 expressions show pattern of elevating and descending to normal under the pressures of 9 mmHg and 12 mmHg. The expressions were different from control group significantly at 24 and 48 hours (P<0.01), while the 72 hours expression showed no difference compared with the control. E-cadherin expression decreased right after treatment compared to the control (P<0.01) but recovered to the level of control at 48 hours (P>0.05). In the 15 mmHg group the changes of CD44V6, ICAM-1 and E-cadherin were more remarkable. CD44V6 and ICAM-1 expressions were increased significantly compared to control right after treatment (P<0.05). E-cadherin expression was decreased even at 48 hours compared to control (P<0.01) but show no significant difference at 72 hours.
Conclussions: In vitro simulated pneumoperitoneum pressures which were usually applied in clinical practices have transient influences on the adhesion molecular expression on gastric cancer cell MKN-45.

Key words

Carbon dioxide pneumoperitoneum; gastric cancer cells; cell adhesion molecule; FACScan

DOI: 10.3978/j.issn.2224-4778.2012.s038