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Shintaro Takao

Researcher at Kobe University

Publications -  76
Citations -  2843

Shintaro Takao is an academic researcher from Kobe University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 15, co-authored 68 publications receiving 1916 citations. Previous affiliations of Shintaro Takao include The Breast Cancer Research Foundation.

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Adjuvant Capecitabine for Breast Cancer after Preoperative Chemotherapy.

TL;DR: After standard neoadjuvant chemotherapy containing anthracycline, taxane, or both, the addition of adjuvant capecitabine therapy was safe and effective in prolonging disease‐free survival and overall survival among patients with HER2‐negative breast cancer who had residual invasive disease on pathological testing.
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Comparison of 2D- and 3D-culture models as drug-testing platforms in breast cancer

TL;DR: 3D- Cultured cells forming dense MCSs may be better than 2D-cultured cells in simulating important tumor characteristics in vivo, namely hypoxia, dormancy, anti-apoptotic features and their resulting drug resistance.
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Neratinib after trastuzumab-based adjuvant therapy in HER2-positive breast cancer (ExteNET): 5-year analysis of a randomised, double-blind, placebo-controlled, phase 3 trial

Miguel Martin, +622 more
- 01 Dec 2017 - 
TL;DR: 1 year of extended adjuvant therapy with neratinib, administered after chemotherapy and trastuzumab, significantly reduced the proportion of clinically relevant breast cancer relapses-ie, those that might lead to death, such as distant and locoregional relapses outside the preserved breast-without increasing the risk of long-term toxicity.
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Adipose-derived stem cells enhance human breast cancer growth and cancer stem cell-like properties through adipsin

TL;DR: It is suggested that adipsin is an important adipokine secreted from mammary adipose tissue that functions as a component of tumor microenvironment and a CSC niche in breast cancers.
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Evidence that portal vein decompression improves survival of canine quarter orthotopic liver transplantation.

TL;DR: The results indicate that, in an extreme RLT, portal hypertension is a risk factor predisposing to graft failure, most likely by increasing microvascular injury after recirculation.