Author

S. E. Hancock

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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Biochemistry· 1 Cancer Biology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

N. Turner· 3 shared A. E. Brandon· 1 shared A. Pang· 1 shared B. K. Zhang· 1 shared B. Mak· 1 shared B. Yau· 1 shared C. Bruce· 1 shared C. Yassmin· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersPhysiology

N. Turner

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Insulin sensitivity is preserved in mice made obese by feeding a high starch diet

A. E. Brandon, L. Small, T.-V. Nguyen, E. Suryana, H. Gong, C. Yassmin, S. E. Hancock, T. Pulpitel, S. Stonehouse, L. Prescott, M. A. Kebede, B. Yau, L.-E. Quek, G. M. Kowalski, C. Bruce, , G. J. Cooney

This study shows that mice fed a high starch diet become obese but remain insulin sensitive, unlike those on a high fat diet, with differences in ceramide levels and lipogenesis contributing to this effect.

bioRxiv · May 25, 2022Physiology

FACS-assisted single-cell lipidome analysis of phosphatidylcholines and sphingomyelins

S. E. Hancock, E. Ding, E. Johansson Beves, T. W. Mitchell, N. Turner

This paper develops a high-throughput method for single-cell lipidomics that quantifies phosphatidylcholines and sphingomyelins using FACS, nanoESI, and shotgun lipidomics, enabling lineage distinction and subtle lipidome differences detection.

bioRxiv · Feb 15, 2022 · PreprintBiochemistry

Inhibition of guanosine monophosphate synthetase (GMPS) blocks glutamine metabolism and prostate cancer growth in vitro and in vivo

Q. Wang, Y. F. Guan, S. E. Hancock, K. Wahi, M. van Geldermalsen, B. K. Zhang, A. Pang, R. Nagarajah, B. Mak, L. G. Horvath, N. Turner, J. Holst

This study shows that inhibiting GMPS reduces glutamine metabolism and prostate cancer growth in vitro and in vivo.

bioRxiv · Sep 7, 2020Cancer Biology