2014 Fiscal Year Final Research Report
Study of immunosuppressive tumor microenvironment and therapeutic strategy in breast cancer
Project/Area Number |
24591925
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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
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Research Institution | Kurume University |
Principal Investigator |
SEKI Naoko 久留米大学, 医学部, 講師 (40226634)
|
Co-Investigator(Kenkyū-buntansha) |
TOH Uhi 久留米大学, 医学部, 講師 (60268901)
FUJII Teruhiko 久留米大学, 医学部, 准教授 (50199288)
KAGE Masayoshi 久留米大学病院, 教授 (80148840)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Keywords | 癌 / 免疫学 |
Outline of Final Research Achievements |
Cancer testis (CT)-antigens were expressed in a large proportion of triple negative (TN)- and ALDH-1 positive breast cancer specimens. NY-ESO-1, MAGE-A10, and MAGE-C1 antigens were immunohistochemically expressed in 6%, 15%, and 12% of patients with primary invasive breast carcinoma, respectively. NY-ESO-1 and MAGE-A10 were preferentially expressed in TN or estrogen receptor negative breast cancers (p<0.05). ALDH-1 expression, which have been reported as predictive marker of cancer stem cells in terms of resistance to chemotherapy, was observed in 22% of tumor specimens, and was most prevalent in the TN breast cancers (p<0.001). Moreover, 41% of ALDH-1 positive specimens were accompanied with expression of any of CT-antigens, some of which showed concomitant expression of CT-antigens and ALDH-1. Because of the limited therapeutic modalities for these phenotypes, significance of CT-antigens expressions should be further studied for beneficial immunotherapy in breast cancer patients.
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Free Research Field |
腫瘍免疫学
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