2016 Fiscal Year Final Research Report
HOXB9 expression in breast cancer predicts efficacy of bevacizumab treatment
Project/Area Number |
26461959
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General surgery
|
Research Institution | Keio University |
Principal Investigator |
Tetsu Hayashida 慶應義塾大学, 医学部(信濃町), 講師 (80327543)
|
Project Period (FY) |
2014-04-01 – 2017-03-31
|
Keywords | 乳癌 / ベバシズマブ / 血管新生 / HOXB9 |
Outline of Final Research Achievements |
Homeobox B9 (HOXB9), a transcriptional factor, regulates developmental processes and tumor progression and has recently been recognized as a strong angiogenic factor in breast cancer progresson. This study aimed to investigate the role of HOXB9 in tumorigenesis and angiogenesis. Bevacizumab, an anti-VEGF antibody, remarkably suppressed tumor proliferation by inhibiting angiogenesis in HOXB9-overexpressing xenografts. HOXB9 promotes the secretion of angiogenic factors, including VEGF, to induce tumor proliferation through microenvironmental communication via IL6 signaling; moreover, silencing of VEGF or IL6 terminates microenvironmental crosstalk. Thus, HOXB9 and IL6 may be surrogate markers for bevacizumab treatment in breast cancer.
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Free Research Field |
乳癌
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