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Yoshiya Horimoto

Researcher at Juntendo University

Publications -  91
Citations -  1095

Yoshiya Horimoto is an academic researcher from Juntendo University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 16, co-authored 71 publications receiving 828 citations. Previous affiliations of Yoshiya Horimoto include Imperial College London.

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ATM and p53 regulate FOXM1 expression via E2F in breast cancer epirubicin treatment and resistance

TL;DR: The data show that ATM and p53 coordinately regulate FOXM1 via E2F to modulate epirubicin response and resistance in breast cancer.
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Carcinoma-Associated Fibroblasts Are a Promising Therapeutic Target

TL;DR: The therapeutic feasibility of targeting tumour-promoting CAFs as well as disrupting heterotypic interactions with other cell types in tumours that may improve the efficacy of current anti-tumour therapies are discussed.
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Emerging roles of the tumor-associated stroma in promoting tumor metastasis

TL;DR: The stroma in human carcinomas consists of extracellular matrix and various types of non-carcinoma cells, mainly leukocytes, endothelial cells, fibroblasts, myofibroblast and bone marrow-derived progenitors, which actively supports tumor growth by stimulating neo-angiogenesis, as well as proliferation and invasion of apposed carcinoma cells.
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Combination of Cancer Stem Cell Markers CD44 and CD24 Is Superior to ALDH1 as a Prognostic Indicator in Breast Cancer Patients with Distant Metastases.

TL;DR: The results raise the possibility of CD44+/24- being a good prognostic marker, one which would allow treatment effects and outcomes to be predicted in patients with recurrent breast cancer.
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Expression profiling and significance of VEGF-A, VEGFR2, VEGFR3 and related proteins in endometrial carcinoma.

TL;DR: Evaluated VEGFR3 expression in tumors may provide prognostic data, and help identify patients who would best benefit from anti-angiogenic therapeutic agents, in the first report showing correlations between the expressions levels of the different receptors.