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Ken Nakagawa

Researcher at Japanese Foundation for Cancer Research

Publications -  142
Citations -  7934

Ken Nakagawa is an academic researcher from Japanese Foundation for Cancer Research. The author has contributed to research in topics: Lung cancer & Adenocarcinoma. The author has an hindex of 37, co-authored 134 publications receiving 7390 citations. Previous affiliations of Ken Nakagawa include Kitasato University.

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RET, ROS1 and ALK fusions in lung cancer.

TL;DR: A multivariate analysis of 1,116 adenocarcinomas containing 71 kinase-fusion–positive adenokcinomas identified four independent factors that are indicators of poor prognosis: age ≥50 years, male sex, high pathological stage and negative kinase -fusion status.
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KIF5B-ALK, a Novel Fusion Oncokinase Identified by an Immunohistochemistry-based Diagnostic System for ALK-positive Lung Cancer

TL;DR: An intercalated antibody-enhanced polymer (iAEP) method that incorporates an intercalating antibody between the primary antibody to ALK and the dextran polymer-based detection reagents should prove suitable for immunohistochemical screening of tumors positive for ALK or ALK fusion proteins among pathologic archives.
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Multiplex Reverse Transcription-PCR Screening for EML4-ALK Fusion Transcripts

TL;DR: A multiplex reverse transcription-PCR system is developed that captures all in-frame fusions between EML4 to exon 20 of ALK to reinforce the importance of accurate diagnosis of E ML4-ALK–positive tumors for the optimization of treatment strategies.
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EML4-ALK Fusion Is Linked to Histological Characteristics in a Subset of Lung Cancers

TL;DR: In the present first investigation of EML4-ALK fusion in a large study of lung cancers, an interesting histotype-genotype relationship is found and the fusion protein could be detected by immunohistochemistry, pointing to possible clinical applications.
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EML4-ALK lung cancers are characterized by rare other mutations, a TTF-1 cell lineage, an acinar histology, and young onset.

TL;DR: EML4-ALK-positive tumors may form a distinct entity among lung adenocarcinomas, characterized by young onset, acinar histology, no or rare mutations in EGFR, KRAS, and TP53, and a TTF-1 cell lineage, all in agreement with the prevalence in non- or light smokers.