Yang Liang, Sun Luguo, Wu Xiuli, Wang Li, Wei Hongfei, Wan Min, Zhang Peiyin, Yu Yongli, Wang Liying
Department of Molecular Biology, Norman Bethune College of Medical Sciences, Jilin University, Changchun, China.
Clin Immunol. 2009 Jun;131(3):426-37. doi: 10.1016/j.clim.2009.01.011. Epub 2009 Feb 23.
In order to develop novel CpG ODNs for the treatment of breast cancer, we have designed a series of CpG ODNs and evaluated their anti-tumor activity in a breast cancer mouse model. Interestingly, a C-class CpG ODN, designated as YW002, showed a vigorous activity on the inhibition of tumor growth in mice and completely cured some of the tumor-bearing mice through injection at tumor draining lymph node (TDLN) area. The expansion of immune cells in the TDLN and tumor and the generation of tumor specific immune memory were found associated with YW002-induced anti-tumor activity in mice. These results indicate that C-class CpG ODN could be developed into a medicament in a monotherapeutic regimen for the treatment of breast cancer through injection at TDLN area in clinic.
为了开发用于治疗乳腺癌的新型CpG寡脱氧核苷酸(ODN),我们设计了一系列CpG ODN,并在乳腺癌小鼠模型中评估了它们的抗肿瘤活性。有趣的是,一种被命名为YW002的C类CpG ODN在抑制小鼠肿瘤生长方面表现出强大的活性,并且通过在肿瘤引流淋巴结(TDLN)区域注射,完全治愈了一些荷瘤小鼠。在TDLN和肿瘤中免疫细胞的扩增以及肿瘤特异性免疫记忆的产生与YW002诱导的小鼠抗肿瘤活性相关。这些结果表明,C类CpG ODN可以在临床上通过在TDLN区域注射开发成为一种单药治疗方案用于治疗乳腺癌的药物。