Author

S. L. Pickard

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

Biology Disciplines

Click to filter author papers

Cancer Biology· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:host-pathogen & immune response· 1 Assay:proteomics· 1

Frequent Co-Authors

F. R. Hirsch· 2 shared H. Yu· 2 shared B. Dome· 1 shared C. J. Rivard· 1 shared C. Rivard· 1 shared D. Dora· 1 shared G. A. Brooks· 1 shared I. San-Millan· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersCancer Biology

F. R. Hirsch

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Role of Lactate in the Regulation of Transcriptional Activity of Breast Cancer-Related Genes and Epithelial-to-Mesenchymal Transition Proteins: A Comparison of MCF7 and MDA-MB-231 Cancer Cell Lines

I. San-Millan, J. L. Martinez, S. L. Pickard, H. Yu, F. R. Hirsch, C. J. Rivard, G. A. Brooks

This study shows that endogenous lactate, not glucose, alters gene and protein expression in breast cancer cell lines, affecting carcinogenesis-related genes and EMT markers.

bioRxiv · Mar 23, 2023 · PreprintCancer Biology

Small Cell Lung Cancer Neuroendocrine Subtypes are Associated with Different Immune Microenvironment and Checkpoint Molecule Distribution

D. Dora, C. Rivard, H. Yu, P. Bunn, K. Suda, S. Ren, S. L. Pickard, V. Laszlo, T. Harko, Z. Megyesfalvi, J. Moldvay, F. R. Hirsch, B. Dome, Z. Lohinai

This study shows that NE-low SCLC tumors have more immune cell infiltration and higher expression of IDO and PVR compared to NE-high tumors, suggesting these as potential immunotherapy targets.

bioRxiv · Feb 2, 2020Cancer Biology