Mohammad R M, al-Katib A, Pettit G R, Sensenbrenner L L
Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan 48202.
Cancer Res. 1994 Jan 1;54(1):165-8.
The immunomodulating effects and antitumor activity of two biological agents, bryostatin 1 (Bryo1) and alpha-interferon, were tested in vitro and in vivo either alone or prior to chemotherapy agents, against a Waldenström's macroglobulinemia tumor line (WSU-WM). Bryol caused a decrease in the expression of CD10, CD19, IgM, Leu10, and CD22 and a temporary growth inhibition as measured by cell cycle analysis. alpha-Interferon did not show any major effects. In vivo, severe combined immunodeficient mice were used to test the activity of the agents against WSU-WM. Bryo1 (i.p.) was given either alone or sequentially with doxorubicin (i.v.), vincristine (i.v.), melphalan (i.v.), and alpha-interferon (i.v.). Bryo1 given 24 h before vincristine or melphalan resulted in the highest tumor growth inhibition, tumor growth delay, and tumor cell kill. Two of five mice receiving Bryo1/vincristine combination were free of tumors > 200 days after treatment and were considered cured. In light of our findings, we recommend that Bryo1 be considered for clinical investigation in human B-cell tumors and might best be given combined with other chemotherapy agents used in the treatment of that disease. Whether Bryo1 is acting as a differentiating agent or as a direct anti-Waldenström's macroglobulinemia tumor agent, remains unclear.
在体外和体内分别单独或在化疗药物之前,测试了两种生物制剂苔藓抑素1(Bryo1)和α干扰素对瓦尔登斯特伦巨球蛋白血症肿瘤细胞系(WSU-WM)的免疫调节作用和抗肿瘤活性。Bryo1导致CD10、CD19、IgM、Leu10和CD22的表达降低,并通过细胞周期分析显示出暂时的生长抑制。α干扰素未显示出任何主要作用。在体内,使用严重联合免疫缺陷小鼠来测试这些制剂对WSU-WM的活性。Bryo1(腹腔注射)单独给药或与阿霉素(静脉注射)、长春新碱(静脉注射)、美法仑(静脉注射)和α干扰素(静脉注射)序贯给药。在长春新碱或美法仑前24小时给予Bryo1导致最高的肿瘤生长抑制、肿瘤生长延迟和肿瘤细胞杀伤。接受Bryo1/长春新碱联合治疗的五只小鼠中有两只在治疗后200多天无肿瘤,被认为治愈。根据我们的研究结果,我们建议考虑将Bryo1用于人类B细胞肿瘤的临床研究,并且最好与用于治疗该疾病的其他化疗药物联合使用。Bryo1是作为分化剂还是直接抗瓦尔登斯特伦巨球蛋白血症肿瘤药物,仍不清楚。