Da Costa M L, Redmond P, Bouchier-Hayes D J
Royal College of Surgeons in Ireland, Department of Surgery, Dublin, Ireland.
Surgery. 1998 Sep;124(3):516-25. doi: 10.1067/msy.1998.89410.
Surgical extirpation of solid tumors may be entirely possible, and the consequence of surgical excision is invariably the release of tumor cells into the systemic circulation. The aim of this study was to determine whether laparotomy affects the establishment of spontaneous pulmonary metastases after excision of the primary tumor in a murine flank tumor model and to determine possible underlying immune abnormalities.
An initial experiment was carried out to compare the development of gross spontaneous pulmonary metastases in the presence of a primary flank tumor and after excision of the tumor in C57/BL6 female mice. Another group of mice had flank tumors excised and were simultaneously randomized to undergo anesthetic only (control), laparoscopy, or laparotomy, after which the subsequent development of pulmonary metastases was determined. Finally, a third experiment entailed determination of natural killer cell (NK) cytotoxicity and the effect of splenic macrophages on NK cytotoxicity at days 1,7, and 14 after tumor excision.
Excision of the primary tumor resulted in a significant increase in the number of pulmonary metastases in mice compared with mice that did not have tumors excised (P = .01). Both laparotomy and laparoscopy significantly increased the number of spontaneous pulmonary metastases after tumor excision compared with controls (P < or = .01), and there was also a significant difference between laparotomy and laparoscopy groups (P = .00). NK cytotoxicity was significantly suppressed at all time points after operation in the laparotomy group compared with both the laparoscopy group and the controls (P < or = .01). Suppression occurred after laparoscopy at 24 hours after the procedure compared with controls (P = .00); by day 7 this difference was not significant, but as day 14 there was again a significant suppression (P < or = .03). Splenic macrophages appeared to be a suppressor to natural killer cell cytotoxicity (NKCC) in the corresponding groups and at the corresponding time points.
The differential establishment of spontaneous metastases after tumor excision and laparotomy and, to a lesser extent, laparoscopy results in lowered host antitumor surveillance and may be mediated at least in part by the generation of splenic suppressor cells in the early postoperative period, causing a more marked and prolonged effect after laparotomy than after laparoscopy.
实体瘤的手术切除或许完全可行,而手术切除的结果必然是肿瘤细胞释放进入体循环。本研究的目的是确定在小鼠侧腹肿瘤模型中,剖腹手术是否会影响原发性肿瘤切除后自发性肺转移的形成,并确定可能潜在的免疫异常情况。
开展了一项初始实验,以比较C57/BL6雌性小鼠存在原发性侧腹肿瘤时以及肿瘤切除后肉眼可见的自发性肺转移的发展情况。另一组小鼠切除侧腹肿瘤后,同时被随机分为仅接受麻醉(对照组)、接受腹腔镜检查或剖腹手术,之后确定肺转移的后续发展情况。最后,第三个实验涉及在肿瘤切除后第1、7和14天测定自然杀伤细胞(NK)的细胞毒性以及脾巨噬细胞对NK细胞毒性的影响。
与未切除肿瘤的小鼠相比,原发性肿瘤切除导致小鼠肺转移数量显著增加(P = 0.01)。与对照组相比,剖腹手术和腹腔镜检查均显著增加了肿瘤切除后自发性肺转移的数量(P≤0.01),并且剖腹手术组和腹腔镜检查组之间也存在显著差异(P = 0.00)。与腹腔镜检查组和对照组相比,剖腹手术组术后所有时间点的NK细胞毒性均受到显著抑制(P≤0.01)。与对照组相比,腹腔镜检查术后24小时出现抑制(P = 0.00);到第7天,这种差异不显著,但到第14天再次出现显著抑制(P≤0.03)。在相应组和相应时间点,脾巨噬细胞似乎是自然杀伤细胞细胞毒性(NKCC)的抑制因子。
肿瘤切除和剖腹手术后自发性转移的不同形成情况,以及在较小程度上腹腔镜检查后自发性转移的不同形成情况,导致宿主抗肿瘤监测降低,并且可能至少部分是由术后早期脾抑制细胞的产生介导的,与腹腔镜检查相比,剖腹手术后产生的影响更显著且持续时间更长。