Author

Y. Shiio

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 2

Signature Assays, Organisms & Methods

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Research Focus:cancer & tumor microenvironment· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

A. Koehne· 1 shared A. M. Houghton· 1 shared B. Freie· 1 shared D. P. MacPherson· 1 shared E. Babaeva· 1 shared E. Eastwood· 1 shared H. Mathsyaraja· 1 shared J. Catchpole· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperCancer Biology

A. Koehne

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2 papers

Recent·Most cited

Loss of MGA mediated Polycomb repression promotes tumor progression and invasiveness

H. Mathsyaraja, J. Catchpole, E. Eastwood, E. Babaeva, M. J. Geuenich, P.-F. Cheng, B. Freie, J. L. Ayers, M. Yu, N. Wu, K. R. Poudel, A. Koehne, W. Grady, A. M. Houghton, Y. Shiio, , R. N. Eisenman

This study shows that loss of MGA promotes tumor growth and invasiveness by de-repressing Polycomb targets in lung and colon cancers.

eLife · Jul 8, 2021Peer-reviewedCancer Biology

EWS-FLI-1 creates a cell surface microenvironment conducive to IGF signaling by inducing pappalysin-1.

P. Jayabal, P. J. Houghton, Y. Shiio

This study shows EWS-FLI-1 promotes IGF signaling by inducing pappalysin-1, which degrades IGFBPs and enhances IGF bioavailability, making pappalysin-1 a potential therapeutic target in Ewing sarcoma.

bioRxiv · Sep 28, 2017Cancer Biology