Heuser L S, Taylor S H, Folkman J
J Surg Res. 1984 Mar;36(3):244-50. doi: 10.1016/0022-4804(84)90094-5.
It has previously been shown that protamine sulfate is an angiogenesis inhibitor. Regional infusion of protamine into the peritoneal cavity is now reported to prevent the growth of intraperitoneal vascularized tumor masses in rats. Walker 256 carcinoma was implanted directly into the liver or into the peritoneal cavity of rats. Hepatic implants grew in the liver with metastases to the wound and mesentery. Injected tumor cells grew as solid tumor masses in the mesentery. Bloody ascites developed after 7 days. Animals received an intraperitoneal infusion of protamine or saline. Protamine significantly inhibited growth of solid tumors in the mesentery (P less than 0.001). Histology showed tumor cells growing only in monolayer but without vascularization. Ascites was not bloody. In saline-treated animals large vascularized tumors grew in the peritoneal cavity and ascites became bloody.
先前已表明硫酸鱼精蛋白是一种血管生成抑制剂。据报道,将鱼精蛋白局部注入大鼠腹腔可防止大鼠腹腔内血管化肿瘤块的生长。将Walker 256癌直接植入大鼠肝脏或腹腔。肝脏植入物在肝脏中生长,并转移至伤口和肠系膜。注射的肿瘤细胞在肠系膜中生长为实体瘤块。7天后出现血性腹水。动物接受腹腔内注入鱼精蛋白或生理盐水。鱼精蛋白显著抑制肠系膜中实体瘤的生长(P小于0.001)。组织学显示肿瘤细胞仅单层生长但无血管化。腹水无血性。在接受生理盐水治疗的动物中,腹腔内生长出大的血管化肿瘤,腹水变为血性。