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Evaluation of Antitumor Activity of Platelet Microbicidal Protein on the Model of Transplanted Breast Cancer in CBRB-Rb(8.17)1Iem Mice

机译:CBRB-Rb(8.17)1Iem小鼠移植性乳腺癌模型中血小板杀微生物蛋白的抗肿瘤活性评估

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摘要

Breast cancer is the most common women's cancer in the world. There is considerable current interest in developing anticancer agents with a new mode of action because of the development of resistance by cancer cells towards current anticancer drugs. Mamalian cells have been shown to contain small, cationic, microbicidal peptides. Antimicrobial peptides have drawn attention as a promising alternative to current antitumor agents. Such peptides have been isolated both from animal and human platelets and have been termed platelets microbicidal proteins (PMP). The aim of this work was to study antitumor activity of PMP in vivo on the model of mouse breast cancer in comparison with antitumor hexapeptide Arg-alpha-Asp-Lys-Val-Tyr-Arg (Immunofan). We demonstrated that the tumors treated with PMP were significant smaller than the control groups (P < 0.05). In experiments in vivo using CBRB-Rb(8.17)1Iem mice with transplanted tumors PMP inhibited tumor growth during the treatments and after its discontinuation. These findings indicate that PMP can exert antitumor effects. Therefore, PMP may be used for the development of therapy for the intervention of breast cancer.
机译:乳腺癌是世界上最常见的女性癌症。由于癌细胞对当前的抗癌药产生了抗药性,因此目前人们对开发具有新作用方式的抗癌药具有相当大的兴趣。哺乳动物细胞已显示含有小的阳离子,杀微生物肽。抗菌肽作为当前抗肿瘤药的一种有前途的替代品已引起关注。这样的肽已经从动物和人血小板中分离出来,并且被称为血小板杀微生物蛋白(PMP)。这项工作的目的是与抗肿瘤六肽Arg-α-Asp-Lys-Val-Tyr-Arg(Immunofan)相比,研究PMP在小鼠乳腺癌模型上的体内抗肿瘤活性。我们证明了用PMP治疗的肿瘤明显小于对照组(P <0.05)。在体内实验中,使用CBRB-Rb(8.17)1Iem小鼠移植了肿瘤,PMP在治疗过程中和停药后均抑制了肿瘤的生长。这些发现表明PMP可以发挥抗肿瘤作用。因此,PMP可用于开发治疗乳腺癌的疗法。

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