Zeng An-Qi, Yu Yan, Yao Yu-Qin, Yang Fang-Fang, Liao Mengya, Song Lin-Jiang, Li Ya-Li, Yu Yang, Li Yu-Jue, Deng Yuan-Le, Yang Shu-Ping, Zeng Chen-Juan, Liu Ping, Xie Yong-Mei, Yang Jin-Liang, Zhang Yi-Wen, Ye Ting-Hong, Wei Yu-Quan
Laboratory of Liver Surgery, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.
Sichuan Nursing Vocational College, Chengdu 610100, China.
Oncotarget. 2017 Dec 17;9(3):3794-3804. doi: 10.18632/oncotarget.23376. eCollection 2018 Jan 9.
Breast cancer is the most common female cancer with considerable metastatic potential, explaining the need for new candidates that inhibit tumor metastasis. In our study, betulinic acid (BA), a kind of pentacyclic triterpenoid compound derived from birch trees, was evaluated for its anti-metastasis activity and . BA decreased the viability of three breast cancer cell lines and markedly impaired cell migration and invasion. In addition, BA could inhibit the activation of stat3 and FAK which resulted in a reduction of matrix metalloproteinases (MMPs), and increase of the MMPs inhibitor (TIMP-2) expression. Moreover, in our animal experiment, intraperitoneal administration of 10 mg/kg/day BA suppressed 4T1 tumor growth and blocked formation of pulmonary metastases without obvious side effects. Furthermore, histological and immunohistochemical analyses showed a decrease in MMP-9 positive cells, MMP-2 positive cells and Ki-67 positive cells and an increase in cleaved caspase-3 positive cells upon BA administration. Notably, BA reduced the number of myeloid-derived suppressor cells (MDSCs) in the lungs and tumors. Interestingly, in our caudal vein model, BA also obviously suppressed 4T1 tumor pulmonary metastases. These findings suggested that BA might be a potential agent for inhibiting the growth and metastasis of breast cancer.
乳腺癌是最常见的具有显著转移潜能的女性癌症,这解释了为何需要新的抑制肿瘤转移的候选药物。在我们的研究中,对源自桦树的一种五环三萜类化合物桦木酸(BA)的抗转移活性进行了评估。BA降低了三种乳腺癌细胞系的活力,并显著损害细胞迁移和侵袭能力。此外,BA可抑制stat3和FAK的激活,从而导致基质金属蛋白酶(MMPs)减少,以及MMPs抑制剂(TIMP - 2)表达增加。此外,在我们的动物实验中,每天腹腔注射10 mg/kg的BA可抑制4T1肿瘤生长并阻止肺转移形成,且无明显副作用。此外,组织学和免疫组化分析显示,给予BA后,MMP - 9阳性细胞、MMP - 2阳性细胞和Ki - 67阳性细胞数量减少,而裂解的caspase - 3阳性细胞数量增加。值得注意的是,BA减少了肺和肿瘤中髓源性抑制细胞(MDSCs)的数量。有趣的是,在我们的尾静脉模型中,BA也明显抑制了4T1肿瘤的肺转移。这些发现表明,BA可能是一种抑制乳腺癌生长和转移的潜在药物。