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Masakazu Toi

Researcher at Kyoto University

Publications -  658
Citations -  28522

Masakazu Toi is an academic researcher from Kyoto University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 69, co-authored 578 publications receiving 23200 citations. Previous affiliations of Masakazu Toi include The Breast Cancer Research Foundation & Tokyo Metropolitan Komagome Hospital.

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Increased estrogen sulfatase (STS) and 17β-hydroxysteroid dehydrogenase type 1(17β-HSD1) following neoadjuvant aromatase inhibitor therapy in breast cancer patients

TL;DR: Significant alterations of intratumoral enzymes, especially 17β-HSD1 and STS, were correlated with Ki67 reduction after neoadjuvant EXE therapy and may represent the compensatory response of breast carcinoma tissues to estrogen depletion.
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Plasma Nucleosome Levels in Node-Negative Breast Cancer Patients.

TL;DR: Increased PNLs were found in breast cancer patients, andPNLs seem promising as a new prognostic factor for both node-negative and node-positive breast cancer.
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Health-Related Quality of Life in MONARCH 2: Abemaciclib plus Fulvestrant in Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer After Endocrine Therapy.

TL;DR: Results support treatment with abemaciclib plus fulvestrant in a population of patients with endocrine-resistant HR+, HER2-negative ABC and impact on health-related quality of life (HRQoL) is important to consider, given the palliative nature of ABC treatment.
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Radicol, a microbial cell differentiation modulator, inhibits in vivo angiogenesis

TL;DR: Results indicate that radicicol might be a potential drug for treating different angiogenesis-dependent diseases, such as solid tumors, psoriasis, rheumatoid arthritis, and diabetic retinopathy.
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Anti-Tumor Activity and Immunotherapeutic Potential of a Bisphosphonate Prodrug.

TL;DR: In this paper, the authors synthesize bisphosphonate prodrugs and found that they efficiently limit tumor cell growth, and that they could enhance the effectiveness of adoptive cancer immunotherapy with γδ T cells.