Author

A. Baggiolini

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· 4

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:human· 4 Organism:zebrafish· 4 Assay:bulk RNA-seq· 3 Research Focus:cell type annotation· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:differential expression· 2 Assay:DNA methylation· 2

Frequent Co-Authors

R. M. White· 4 shared E. Montal· 3 shared L. Studer· 3 shared N. R. Campbell· 3 shared T.-H. Huang· 3 shared Y. Ma· 3 shared B. S. Taylor· 2 shared D. Lumaquin· 2 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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4 shared papersCancer Biology

R. M. White

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4 papers

Recent·Most cited

Epigenetic reprogramming of melanoma cell state through fatty acid β-oxidation and Toll like receptor 4 signaling

T.-H. Huang, Y. Ma, E. Montal, S. Suresh, M. M. Tagore, A. Corbin, D. Lumaquin, N. R. Campbell, A. Baggiolini, R. P. Koche, R. M. White

This study shows that fatty acid β-oxidation and TLR4 signaling drive melanoma progression by altering histone acetylation and inflammatory gene expression.

bioRxiv · Jun 16, 2022 · PreprintCancer Biology

Lipid droplets are a metabolic vulnerability in melanoma

D. Lumaquin, E. Montal, A. Baggiolini, Y. Ma, C. LaPlante, T.-H. Huang, S. Suresh, L. Studer, R. M. White

This study identifies lipid droplets as a metabolic vulnerability in melanoma by linking the pigmented cell state to increased fatty acid uptake and oxidative metabolism.

bioRxiv · May 4, 2022 · PreprintCancer Biology

Anatomic position determines oncogenic specificity in melanoma

J. M. Weiss, M. V. Hunter, N. M. Cruz, A. Baggiolini, M. Tagore, Y. Ma, S. Misale, M. Marasco, T. Simon-Vermot, N. R. Campbell, F. Newell, J. S. Wilmott, P. A. Johansson, J. F. Thompson, G. V. Long, , R. M. White

The paper shows that anatomic position influences oncogenic specificity in melanoma by identifying position-specific gene programs that interact with oncogenes like CRKL.

bioRxiv · Nov 14, 2020Cancer Biology

Developmental chromatin programs determine oncogenic competence in melanoma

A. Baggiolini, S. J. Callahan, T. Trieu, M. M. Tagore, E. Montal, J. M. Weiss, S. E. Tischfield, Y. Fan, N. R. Campbell, N. Saurat, T. Hollmann, T. Simon-Vermot, S. K. Tickoo, B. S. Taylor, R. Koche, , R. M. White

The paper shows that BRAFV600E transforming ability depends on the cell of origin's transcriptional program, with neural crest and melanoblasts being more susceptible due to higher chromatin modifying enzyme expression and ATAD2-SOX10 complex formation.

bioRxiv · May 9, 2020Cancer Biology