Thursday, August 28
Welcome address
09:00-09:05 Weng-Onn Lui, John Paoli, Nicole Fischer, Jürgen Becker, Lisa Villabona & Thibault Kervarrec
Session I: Merkel cell polyomavirus and oncogenesis
Chair: Nicole Fischer (Hamburg-Eppendorf, Germany) and Ugo Moens (Tromsø, Norway)
09:05-09:35 Nick Salisbury (Seattle, WA, USA)
LT/E2F and ALTO/NF-κB signaling control the switch between MCPyV replication and latency
09:35-10:05 Étienne Coyaud (Lille, France)
Proximal interactomics approaches to explore MCC oncogenes molecular mechanisms
10:05-10:35 John Charles Rotondo (Genoa, italy)
Epigenetic dysregulation in MCC: a potential therapeutic target
10:35-10:50 Isaac Brownell (Bethesda, MD, USA)
The paranuclear dot as a regulator of extrinsic apoptosis
10:50-11:20 Coffee break
11:20-11:35 Amanda Macamo (Maastricht, The Netherlands)
Restoring the B-cell identity in MCC
11:35-12:00 Flash poster presentations (3 minutes/presentation)
Brendan McCann (Glasgow, Scotland, UK), Candice Church (Seattle, WA, USA), Sara Passerini (Rome, Italy), Xiaohao Wang (Stockholm, Sweden), Büke Celikdemir (Würzburg, Germany), Peter Ch’en (Seattle, WA, USA) and Libuše Janská (Stockholm, Sweden).
12:00-12:45 Poster session
12:45-13:45 Lunch
Session II: Immunobiology and tumor microenvironment
Chairs: Thibault Kervarrec (Tours, France) and John Paoli (Gothenburg, Sweden)
13:45-14:15 Maximilian Haist (Palo Alto, CA, USA)
MCPyV-linked spatial Immunomodulation of the MCC tumor microenvironment and its impact on patient survival
14:15-14:45 Jaehyuk Choi (Dallas, TX, USA)
Immune landscape of MCCs
14:45-15:15 Göran Jönsson (Lund, Sweden)
The role of tertiary lymphoid structures in cancer immunity
15:15-15:45 Coffee break
15:45-16:00 Tomas Bencomo (Seattle, WA, USA)
Spatial transcriptomics analysis of MCC reveals tumor-intrinsic factors involved in T cell exclusion
16:00-16:15 Paul Harms (Ann Arbor, MI, USA)
The Diagnostic Utility of H3K27Me3 Immunohistochemistry for MCC
16:15-16:30 Haroldo Rodríguez (Seattle, WA, USA)
B cells specific for polyomavirus-derived oncoprotein are predictive of MCC progression