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免疫佐剂肽聚糖单体PGM对荷MCa乳腺癌小鼠的抗肿瘤和抗转移活性

Antitumor and antimetastatic activity of the immunoadjuvant peptidoglycan monomer PGM in mice bearing MCa mammary carcinoma.

作者信息

Sava G, Tomasic J, Hrsak I

出版信息

Cancer Immunol Immunother. 1984;18(1):49-53. doi: 10.1007/BF00205399.

Abstract

The antitumor and antimetastatic activities of the water-soluble peptidoglycan monomer GlnNAc-Mur-NAc-L-Ala-D-iso-Gln-meso-diamminopimelic acid (omega-NH2)-D-Ala-D-Ala (PGM), which has immunostimulant effects, have been evaluated in CBA mice bearing MCa mammary carcinoma. The antineoplastic effects of PGM depend strictly on the dosage and treatment schedule used. Though a significant inhibition of the primary tumor growth is observed over a wide range of dosage, only the IV administration of daily doses of 50 mg/kg/day on days 1, 5, 10, 15 inhibits spontaneous lung metastasis formation and in parallel prolongs the survival time of the treated mice. The magnitude of the antimetastatic effects of PGM depends on the degree of dissemination of the tumor, and is greater when the number of metastatic foci is low. Examination of the therapeutic potential of PGM in combination with surgery has further indicated that the timing of administration plays an important role in the overall effectiveness of this substance. A 5-day interval is necessary between two consecutive injections for the induction of significant increases of the survival times.

摘要

具有免疫刺激作用的水溶性肽聚糖单体GlnNAc-Mur-NAc-L-Ala-D-异-Gln-内消旋二氨基庚二酸(ω-NH2)-D-Ala-D-Ala(PGM)的抗肿瘤和抗转移活性已在携带MCa乳腺癌的CBA小鼠中进行了评估。PGM的抗肿瘤作用严格取决于所用的剂量和治疗方案。虽然在很宽的剂量范围内都观察到对原发性肿瘤生长有显著抑制作用,但只有在第1、5、10、15天静脉注射每日剂量50mg/kg/天才能抑制自发性肺转移的形成,并同时延长治疗小鼠的存活时间。PGM抗转移作用的大小取决于肿瘤的扩散程度,当转移灶数量较少时作用更强。对PGM与手术联合治疗潜力的研究进一步表明,给药时间对该物质的整体疗效起着重要作用。连续两次注射之间需要间隔5天才能显著延长存活时间。

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