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Kuniko Matsuda

Researcher at Nippon Medical School

Publications -  47
Citations -  1423

Kuniko Matsuda is an academic researcher from Nippon Medical School. The author has contributed to research in topics: Lung cancer & Idiopathic pulmonary fibrosis. The author has an hindex of 18, co-authored 43 publications receiving 1235 citations. Previous affiliations of Kuniko Matsuda include University of Tsukuba.

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MiR-134/487b/655 Cluster Regulates TGF-β–Induced Epithelial–Mesenchymal Transition and Drug Resistance to Gefitinib by Targeting MAGI2 in Lung Adenocarcinoma Cells

TL;DR: This study demonstrated that the miR-134/487b/655 cluster contributed to the TGF-β1–induced EMT phenomenon and affected the resistance to gefitinib by directly targeting MAGI2, in which suppression subsequently caused loss of PTEN stability in lung cancer cells.
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Reduction of PTEN protein and loss of epidermal growth factor receptor gene mutation in lung cancer with natural resistance to gefitinib (IRESSA).

TL;DR: The data suggests that the EGFR gene mutation may be possibly lost in some cancer cells with other additional mechanisms for activating Akt, and reintroduction of PTEN or pharmacological downregulation of the constitutive PI3K–Akt-pathway activity may be an attractive therapeutic strategy in cancers with gefitinib resistance.
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Pirfenidone inhibits fibrocyte accumulation in the lungs in bleomycin-induced murine pulmonary fibrosis

TL;DR: Pirfenidone significantly ameliorated bleomycin-induced pulmonary fibrosis as assessed with quantitative histology and collagen measurement, and fibrocyte inhibition is considered a mechanism of anti-fibrotic action of pirfenid one.
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Antitumor activity of histone deacetylase inhibitors in non-small cell lung cancer cells: development of a molecular predictive model

TL;DR: The results suggested that HDAC inhibitors may be promising anticancer drugs to NSCLC and the nine-gene classifier is useful in predicting drug sensitivity to HDAC inhibitor treatment and may contribute to achieving individualized therapy for NS CLC patients.