Toshitaka Nagao

Dr. Toshitaka Nagao

Department of Anatomic Pathology, Tokyo Medical University, Tokyo 1600023, Japan
orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2012 in ACTA HISTOCHEMICA ET CYTOCHEMICA
Verified
Journal Article
Open access
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Toshitaka NagaoToshitaka Nagao
Toshitaka Nagao
ESEiichi Sato
Eiichi Sato
RIRie Inoue
Rie Inoue
HOHisashi Oshiro
Hisashi Oshiro
RTReisuke H. Takahashi
Reisuke H. Takahashi
JMJun Matsubayashi
Jun Matsubayashi
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societies

18 May 2020 in Cancer Cytopathology
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Journal Article
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MNMasato Nakaguro
Masato Nakaguro
YTYuichiro Tada
Yuichiro Tada
WFWilliam Faquin
William Faquin
PSPeter M. Sadow
Peter M. Sadow
LWLori J. Wirth
Lori J. Wirth
Toshitaka NagaoToshitaka Nagao
Toshitaka Nagao

3 July 2013 in Head and Neck Pathology
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Journal Article
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Toshitaka NagaoToshitaka Nagao
Toshitaka Nagao
“Dedifferentiation” and/or high-grade transformation (HGT) has been described in a variety of salivary gland carcinomas, including acinic cell carcinoma, adenoid cystic carcinoma, epithelial-myoepithelial carcinoma, polymorphous low-grade adenocarcinoma, myoepithelial carcinoma, low-grade mucoepidermoid carcinoma and hyalinizing clear cell carcinoma, although the phenomenon is a rare event. Recent authors tend to preferably use the term HGT instead of “dedifferentiation” in these cases. HGT-tumors are composed of conventional carcinomas juxtaposed with areas of HG morphology, usually either poorly differentiated adenocarcinoma or “undifferentiated” carcinoma, in which the original line of differentiation is no longer evident. The HG component is generally composed of solid nests, sometimes occurring in cribriform pattern of anaplastic cells with large vesicular pleomorphic nuclei, prominent nucleoli and abundant cytoplasm. Frequent mitoses and extensive necrosis is evident. The Ki-67 labeling index is consistently higher in the HG component. p53 abnormalities have been demonstrated in the transformed component in a few examples, but the frequency varies by the histologic type. HER-2/neu overexpression and/or gene amplification is considerably exceptional. The molecular-genetic mechanisms responsible for the pathway of HGT in salivary gland carcinomas largely still remain to be elucidated. Salivary gland carcinomas with HGT have been shown to be more aggressive than conventional carcinomas with a poorer prognosis, accompanied by higher local recurrence rate and propensity for cervical lymph node metastasis, suggesting the need for wider resection and neck dissection.

2 August 2017 in Oncotarget
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Journal Article
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STSoichiro Takase
Soichiro Takase
SKSatoshi Kano
Satoshi Kano
YTYuichiro Tada
Yuichiro Tada
DKDaisuke Kawakita
Daisuke Kawakita
TSTomotaka Shimura
Tomotaka Shimura
Toshitaka NagaoToshitaka Nagao
Toshitaka Nagao
Biomarker immunoprofile in salivary duct carcinomas: clinicopathological and prognostic implications with evaluation of the revised classification Biomarker immunoprofile in salivary duct carcinomas: clinicopathological and prognostic implications with evaluation of the revised classification

10 September 2019 in Histopathology
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Journal Article
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MNMasato Nakaguro
Masato Nakaguro
MUMakoto Urano
Makoto Urano
IOIkuko Ogawa
Ikuko Ogawa
HHHideaki Hirai
Hideaki Hirai
YYYoshinari Yamamoto
Yoshinari Yamamoto
Toshitaka NagaoToshitaka Nagao
Toshitaka Nagao

4 December 2017 in Oncotarget
Verified
Journal Article
Open access
PDF file
TSTomotaka Shimura
Tomotaka Shimura
YTYuichiro Tada
Yuichiro Tada
HHHideaki Hirai
Hideaki Hirai
DKDaisuke Kawakita
Daisuke Kawakita
SKSatoshi Kano
Satoshi Kano
Toshitaka NagaoToshitaka Nagao
Toshitaka Nagao
Prognostic and histogenetic roles of gene alteration and the expression of key potentially actionable targets in salivary duct carcinomas Prognostic and histogenetic roles of gene alteration and the expression of key potentially actionable targets in salivary duct carcinomas