共 51 条
Inhibition of breast cancer growth and metastasis by a biomimetic peptide
被引:34
作者:

Lee, Esak
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Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA

Lee, Seung Jae
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Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA

Koskimaki, Jacob E.
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Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA

Han, Zheyi
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Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA

Pandey, Niranjan B.
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Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA

Popel, Aleksander S.
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Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21231 USA
Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
机构:
[1] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
来源:
基金:
美国国家卫生研究院;
关键词:
RECEPTOR TYROSINE KINASE;
LYMPH-NODE METASTASIS;
C-MET;
COLLAGEN-IV;
CELL PROLIFERATION;
LYMPHANGIOGENESIS;
ANGIOGENESIS;
EXPRESSION;
MIGRATION;
ACTIVATION;
D O I:
10.1038/srep07139
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Metastasis is the main cause of mortality in cancer patients. Though there are many anti-cancer drugs targeting primary tumor growth, anti-metastatic agents are rarely developed. Angiogenesis and lymphangiogenesis are crucial for cancer progression, particularly, lymphangiogenesis is pivotal for metastasis in breast cancer. Here we report that a novel collagen IV derived biomimetic peptide inhibits breast cancer growth and metastasis by blocking angiogenesis and lymphangiogenesis. The peptide inhibits blood and lymphatic endothelial cell viability, migration, adhesion, and tube formation by targeting IGF1R and Met signals. The peptide blocks MDA-MB-231 tumor growth by inhibiting tumor angiogenesis in vivo. Moreover, the peptide inhibits lymphangiogenesis in primary tumors. MDA-MB-231 tumor conditioned media (TCM) was employed to accelerate spontaneous metastasis in tumor xenografts, and the anti-metastatic activity of the peptide was tested in this model. The peptide prevents metastasis to the lungs and lymph nodes by inhibiting TCM-induced lymphangiogenesis and angiogenesis in the pre-metastatic organs. In summary, a novel biomimetic peptide inhibits breast cancer growth and metastasis by blocking angiogenesis and lymphangiogenesis in the pre-metastatic organs as well as primary tumors.
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