Naoya Yamashita

发表

The Differential Selectivity of Aryl Hydrocarbon Receptor (AHR) Agonists towards AHR-Dependent Suppression of Mammosphere Formation and Gene Transcription in Human Breast Cancer Cells.

K. Yoshinari, K. Nemoto, Yuichiro Kanno, 2021, Biological & pharmaceutical bulletin.

Camalexin, an indole phytoalexin, inhibits cell proliferation, migration, and mammosphere formation in breast cancer cells via the aryl hydrocarbon receptor

R. Kizu, Yuichiro Kanno, C. Taga, 2021, Journal of Natural Medicines.

Euphorins A–H: bioactive diterpenoids from Euphorbia fischeriana

Wei Li, K. Koike, Shoko Kikkawa, 2016, Journal of Natural Medicines.

Androgen receptor functions as a negative transcriptional regulator of DEPTOR, mTOR inhibitor.

K. Nemoto, Yuichiro Kanno, Y. Inouye, 2015, The Journal of toxicological sciences.

Cell Cycle and Apoptosis Regulator 1, CCAR1, Regulates Enhancer-Dependent Nuclear Receptor CAR Transactivation

K. Nemoto, Yuichiro Kanno, Y. Inouye, 2018, Molecular Pharmacology.

Possible Involvement of the Upregulation of ΔNp63 Expression Mediated by HER2-Activated Aryl Hydrocarbon Receptor in Mammosphere Maintenance

T. Hosaka, K. Yoshinari, K. Nemoto, 2022, International journal of molecular sciences.

FDI-6, a FOXM1 inhibitor, activates the aryl hydrocarbon receptor and suppresses tumorsphere formation.

R. Kizu, Yuichiro Kanno, Noriko Sanada, 2022, Biochemical and biophysical research communications.

Aryl hydrocarbon receptor counteracts pharmacological efficacy of doxorubicin via enhanced AKR1C3 expression in triple negative breast cancer cells.

N. Hiruta, H. Bujo, K. Nemoto, 2019, Biochemical and biophysical research communications.

Euphorins A–H: bioactive diterpenoids from Euphorbia fischeriana

Wei Li, K. Koike, Shoko Kikkawa, 2016, Journal of Natural Medicines.

ent-Atisane diterpenoids from Euphorbia fischeriana inhibit mammosphere formation in MCF-7 cells

Wei Li, K. Koike, K. Nemoto, 2015, Journal of Natural Medicines.

Tripartite Motif Containing 24 Acts as a Novel Coactivator of the Constitutive Active/Androstane Receptor

Saori Kobayashi, K. Nemoto, Yuichiro Kanno, 2018, Drug Metabolism and Disposition.

Picrasidine G decreases viability of MDA-MB 468 EGFR-overexpressing triple-negative breast cancer cells through inhibition of EGFR/STAT3 signaling pathway.

Wei Li, K. Koike, K. Nemoto, 2017, Bioorganic & medicinal chemistry letters.

Identification of 10-dehydrooxyglycyuralin E as a selective human estrogen receptor alpha partial agonist.

Wei Li, K. Koike, Jian Wang, 2019, Bioorganic chemistry.

An androgen-independent mechanism underlying the androgenic effects of 3-methylcholanthrene, a potent aryl hydrocarbon receptor agonist.

R. Kizu, Yuka Gotoh-Kinoshita, Noriko Sanada, 2020, Toxicology research.

Alisol B 23-acetate from the rhizomes of Alisma orientale is a natural agonist of the human pregnane X receptor.

Wei Li, K. Koike, K. Nemoto, 2017, Phytomedicine : international journal of phytotherapy and phytopharmacology.

Activation of the aryl hydrocarbon receptor by 3-methylcholanthrene, but not by indirubin, suppresses mammosphere formation via downregulation of CDC20 expression in breast cancer cells.

K. Nemoto, R. Kizu, Yuichiro Kanno, 2021, Biochemical and Biophysical Research Communications - BBRC.

Camalexin, an indole phytoalexin, inhibits cell proliferation, migration, and mammosphere formation in breast cancer cells via the aryl hydrocarbon receptor

R. Kizu, Yuichiro Kanno, C. Taga, 2021, Journal of Natural Medicines.

Tripartite Motif Containing 24 Acts as a Novel Coactivator of the Constitutive Active/Androstane Receptor

Saori Kobayashi, K. Nemoto, Yuichiro Kanno, 2018, Drug Metabolism and Disposition.