Natural product Eriocalyxin B suppressed triple negative breast cancer metastasis both in vitro and in vivo

被引:13
作者
Gou, Leilei [1 ,4 ]
Yue, Grace Gar-Lee [2 ,3 ]
Lee, Julia Kin -Ming [2 ,3 ]
Puno, Pema Tenzin [1 ,5 ]
Lau, Clara Bik-San [2 ,3 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Chi, Kunming 650201, Yunnan, Peoples R China
[2] Chinese Univ Hong Kong, Inst Chinese Med, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, State Key Lab Res Bioact & Clin Applicat Med Plant, Shatin, Hong Kong, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Chinese Acad Sci, Kunming Inst Bot, Kunming 650201, Yunnan, Peoples R China
关键词
Breast cancer; Metastasis; Natural products; Eriocalyxin B; Cancer recurrence; Cancer stem cells; Gut microbiome; NF-KAPPA-B; STEM-CELLS; MOLECULAR-MECHANISMS; EXTRACELLULAR-MATRIX; TUMOR-GROWTH; APOPTOSIS; ANGIOGENESIS; PROGRESSION; CARCINOMA; LEUKEMIA;
D O I
10.1016/j.bcp.2023.115491
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Breast cancer is the most commonly diagnosed cancer among women, and its metastasis to distant organs accounts for the majority of death. Eriocalyxin B (Eri B), an ent-kaurane diterpenoid isolating from Isodon eriocalyx var. laxiflora, has previously been reported to have anti-tumor and anti-angiogenic effects in breast cancer. Here, we investigated the effect of Eri B on cell migration and adhesion in triple negative breast cancer (TNBC) cells, as well as aldehyde dehydrogenases 1 family member A1 (ALDH1A1) expression, colony- and sphere-formation in cancer stem cell (CSC) enriched MDA-MB-231 cells. The in vivo anti-metastatic activities of Eri B were determined in 3 different breast tumor-bearing mouse models. Our results indicated that Eri B inhibited TNBC cell migration and adhesion to extracellular matrix proteins, and also reduced ALDH1A1 expression and colony formation in CSC-enriched MDA-MB-231 cells. The metastasis-related pathways, such as epidermal growth factor receptor/ mitogen-activated protein kinase kinases 1/2/ extracellular regulated protein kinase signaling altered by Eri B was firstly shown in MDA-MB-231 cells. The potent anti-metastatic efficacies of Eri B were demonstrated in breast xenograft-bearing mice and syngeneic breast tumor-bearing mice. Gut microbiome analysis results revealed the change in the diversity and composition of microbiome after Eri B treatment, and the potential pathways that are involved in the anti-cancer efficacy of Eri B. In conclusion, Eri B was shown to inhibit breast cancer metastasis in both in vitro and in vivo models. Our findings further support the development of Eri B as an anti-metastatic agent for breast cancer.
引用
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页数:15
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