Author

Thais Satie Iijima

Universidade de São PauloORCID 0009-0002-6742-0846Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Sayuri MiyamotoiD· 3 shared Alex InagueiD· 2 shared Larissa Regina DiniziD· 2 shared Lucas Gasparello VivianiiD· 2 shared Luís Eduardo Soares NettoiD· 2 shared Rodrigo Santiago LimaiD· 2 shared Thiago Gerônimo Pires AlegriaiD· 2 shared Adriana MañasiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersBiochemistry

Sayuri MiyamotoORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BiochemistryPhotochemistry and PhotobiologyPeer-reviewedJan 21, 2025

Comparative study of Ergosterol and 7-dehydrocholesterol and their Endoperoxides: Generation, Identification and Impact in Phospholipid Membranes and Melanoma Cells

Megumi Nishitani Yukuyama, Karen Campos Fabiano, Alex Inague…·Sayuri Miyamoto

This study compares the effects of ergosterol, 7-dehydrocholesterol, and cholesterol under oxidative stress in melanoma cells, showing endoperoxides from these sterols are more effective in reducing cell viability.

8 citationstop 5%

humanproteomics

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BiochemistryJournal of Medicinal ChemistryPeer-reviewedDec 19, 2024

Identification of novel human 15-lipoxygenase-2 (h15-LOX-2) inhibitors using a virtual screening approach

Lucas Gasparello Viviani, Thais Satie Iijima, Erika Piccirillo…·Sayuri Miyamoto

This study identifies six novel h15-LOX-2 inhibitors using virtual screening from a curated ZINC database, with two showing micromolar potency and a mixed-type inhibition mechanism.

9 citations

humandeep learning

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Cell BiologyMolecular CellPeer-reviewedNov 14, 2024

PRDX6 contributes to selenocysteine metabolism and ferroptosis resistance

Zhiyi Chen, Alex Inague, Kamini Kaushal…·José Pedro Friedmann Angeli

The paper identifies PRDX6 as an alternative pathway for selenocysteine metabolism that contributes to ferroptosis resistance in cancer cells.

88 citationstop 1%

humanproteomics

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