Author

Elyse G. Schechter

University of ChicagoORCID 0000-0001-6967-3762Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Organism:human· 2 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:genetic perturbation / CRISPR· 1 Approach:statistical model· 1

Frequent Co-Authors

Alpaslan TasdoganiD· 1 shared Brandon FaubertiD· 1 shared Brianna K. ChangiD· 1 shared Christine M. BestvinaiD· 1 shared Clint A. StalneckeriD· 1 shared Emanuel F Petricoin· 1 shared Hardik ShahiD· 1 shared Jonathan M. DeLibertyiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCancer Biology

Alpaslan TasdoganORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Cancer BiologybioRxivPreprintSep 22, 2026

MCT1 activity defines an aggressive metabolic phenotype and therapeutic target in non-small cell lung cancer

Robert B Cameron, Kristen Erika Shema, Nathan Dubois…·Brandon Faubert

This study shows that MCT1-mediated lactate uptake sustains nucleotide homeostasis in NSCLC, and its inhibition enhances chemotherapy efficacy by exposing a metabolic vulnerability.

DOI 10.64898/2026.09.20.752999

humanbulk RNA-seq

𝕏 PostBluesky

Cancer BiologybioRxivPreprintJun 29, 2026

Vertical inhibition of the autophagy pathway impairs growth and enhances sensitivity to mTORC1 inhibition in pancreatic ductal adenocarcinoma

Mallory K. Roach, Seamus E. Degan, Jonathan M. DeLiberty…·Kirsten L. Bryant

This study identifies that vertical inhibition of the autophagy pathway enhances sensitivity to mTORC1 inhibition in PDAC, improving therapeutic efficacy.

DOI 10.64898/2026.06.28.734981

humanbulk RNA-seq

𝕏 PostBluesky