Konno H, Arai T, Tanaka T, Baba M, Matsumoto K, Kanai T, Nakamura S, Baba S, Naito Y, Sugimura H, Yukita A, Asano M, Suzuki H
Second Department of Surgery, Hamamatsu University School of Medicine.
Jpn J Cancer Res. 1998 Sep;89(9):933-9. doi: 10.1111/j.1349-7006.1998.tb00651.x.
Distant metastasis of gastrointestinal endocrine neoplasm is resistant to currently available treatments. Because hematogenic metastasis is dominant, anti-angiogenic drugs are expected to be a novel therapy for this neoplasm. In the present study, the therapeutic effect of vascular endothelial growth factor neutralizing antibody (VEGFAb) on liver metastasis of an endocrine neoplasm was investigated experimentally. Cecal transplantation into nude mice of small pieces of EN-1, a xenotransplanted human intestinal endocrine neoplasm, resulted in liver metastasis. A treated group (n = 19) received 100 micrograms/mouse of VEGFAb intraperitoneally on alternate days from day 10 after tumor transplantation, and the control group (n = 19) received saline. Five of the 19 control mice died of tumor progression, of which 2 could not be evaluated. The cecal tumor weighed 6316 +/- 2333 mg (n = 17) in the control group and 1209 +/- 837 mg (n = 19) in the treated group (P < 0.01) 6 weeks after transplantation. Liver metastasis developed in 16 of 17 control mice and in 2 of 19 treated mice (P < 0.01). The VEGF level of the whole cecal tumor in the control group was significantly higher than that in the treated group (305.1 +/- 174.1 vs. 54.7 +/- 41.2 mg; P < 0.001). VEGFAb did not cause any body weight loss (28.52 +/- 1.63 in the control vs. 28.44 +/- 1.71 g in the treated group). These results indicate that VEGFAb may be a novel therapeutic agent for endocrine neoplasm with distant metastasis.
胃肠道内分泌肿瘤的远处转移对目前可用的治疗方法具有抗性。由于血行转移占主导,抗血管生成药物有望成为治疗这种肿瘤的新疗法。在本研究中,通过实验研究了血管内皮生长因子中和抗体(VEGFAb)对内分泌肿瘤肝转移的治疗效果。将人异种移植肠道内分泌肿瘤EN-1的小块组织移植到裸鼠盲肠中,导致肝转移。治疗组(n = 19)在肿瘤移植后第10天开始每隔一天腹腔注射100微克/只的VEGFAb,对照组(n = 19)注射生理盐水。19只对照小鼠中有5只因肿瘤进展死亡,其中2只无法评估。移植6周后,对照组盲肠肿瘤重6316±2333毫克(n = 17),治疗组为1209±837毫克(n = 19)(P < 0.01)。17只对照小鼠中有16只发生肝转移,19只治疗小鼠中有2只发生肝转移(P < 0.01)。对照组整个盲肠肿瘤的VEGF水平显著高于治疗组(305.1±174.1对54.7±41.2毫克;P < 0.001)。VEGFAb未导致任何体重减轻(对照组为28.52±1.63克,治疗组为28.44±1.71克)。这些结果表明,VEGFAb可能是治疗远处转移内分泌肿瘤的新型治疗药物。