APPENDIX A: WORKSHOP PROGRAMME
Programme Day 1 – Morning |
10:00-10:30 | Registration and welcome coffee |
10:30-10:40 | Welcome and Introduction Alan Poole ECETOC Secretary General |
Session 1: Understanding ncRNAs | |
10:40-11:00
15 minutes + |
What are ncRNAs? Tim Gant PHE, UK - Definitions - Spectrum of ncRNA (sizes, biogenesis) |
11:05-12:00
15 minutes + 5 min Q&A
15 minutes + 5 min Q&A
15 minutes + 5 min Q&A |
What do they do?
- Mechanism of action, Functional Relevance Gunter Meister - Expression of macroscopic phenotypes for miRNA-guided Hervé Seitz
- Cellular adaptation – relevance for risk assessment Emma Marczylo |
12:00-12:20
15 minutes + |
Stability and transport Kenneth Witwer Johns Hopkins University - Cross-kingdom RNA Effect School of Medicine, USA |
Programme Day 1 – Morning (cont’d) |
12:20-12:40
15 minutes + 5 min Q&A |
Cause or Consequence? Jörg Hackermüller UFZ, Germany - What are the links between ncRNA, changes in ncRNA, expression and pathological phenotype |
12:40-13:00
15 minutes + |
Exposure effects? Nigel Gooderham Imperial College London, UK - Relevance of dose level / time / no effect level / adverse effect level |
13:00-14:00 | Lunch |
Programme Day 1 – Afternoon |
Session 2: Understanding possible links between changes in ncRNA and pathology |
|
14:00-14:20
15 minutes + |
ncRNA Therapy Achim Aigner Leipzig University,Germany - Upcoming medical applications - What are the current medical applications of ncRNAs? - How can this help inform toxicology and risk assessment science? - Species differences: do animal models inform about human pathology? |
14:20-14:40
15 minutes + |
Biomarkers Mohamed Benahmed UNICE, France - Technical issues around ncRNAs as biomarkers, (biomonitoring – fluids, and link to pathology – cells/tissues/organs) |
Programme Day 1 – Afternoon (cont’d) |
Session 3: Technical issues around ncRNA in Risk Assessment | |
14:40-15:00
15 minutes + 5 min Q&A |
Data analysis Frank Slack BIDMC Cancer Center Harvard Medical School, USA - What are the key analysis methods currently employed? - Is there a need for harmonisation? - Contamination: is what you are measuring actually what you think you are measuring? |
15:00-15:30 | Coffee |
15:30-16:00
20 minutes discussion + |
Panel Discussion Moderator: Saskia van der Vies VU University Medical Centre, NL Data Interpretation of ncRNAs as biomarkers Panel: - There is an explosion of ncRNA data available, Tim Gant, PHE CRCE |
16:00-16:20
15 minutes + |
Risk Assessment considerations for ncRNA in Jan Verhaert agricultural products/applications Monsanto, Belgium - Current agricultural applications of ncRNA |
16:20-17:00 | Conclusions of Day 1 Alan Poole Details for Networking Cocktail and Day 2 ECETOC SG |
17:00 | Close |
18:00-19:00 | Networking Cocktail |
Programme Day 2 – Morning |
09:30-09:40 | Welcome, Proceedings for Day 2 Alan Poole ECETOC, Belgium |
09:40-10:00 | Summary of Day 1 Saskia van der Vies VU University Medical Center, NL |
10:00-11:00 | Breakout Session 1: Role of ncRNAs in toxicology and risk assessment |
Each breakout group brainstorms both these questions.
Sub-questions are a guide to prompt discussion |
Moderator: Tim Gant / Rapporteur: Madeleine Laffont
Moderator: Roland Buesen / Rapporteur: Achim Aigner Moderator: Helmut Greim / Rapporteur: Alan Poole
1. How to make use of ncRNA technology in toxicology and chemicals risk assessment? - What is relevant and not relevant? - What do ncRNAs really tell us? - How far do ncRNAs really add information to toxicology and risk assessment? - What role for ncRNAs in toxicology and chemicals risk assessment in the next
2. In light of what we know about ncRNas – should we re-evaluate current toxicology and chemicals risk assessment?
- What do changes in ncRNA mean regarding the phenotype? - What is relevant (cross-kingdom RNA effects)? - What are the implications for industry/regulations? - Are the changes in the expression of ncRNA helpful in our |
11:00-11:30 | Coffee |
Programme Day 2 – Morning (cont’d) |
11:30-12:30 | Plenary:
Moderators share findings from breakout sessions, with room for audience discussion |
|
12:30-12:45 | Afternoon session explained | Madeleine Laffont ECETOC |
12:45-13:00 | Cefic LRI Programme explained | Bruno Hubesch Cefic-LRI |
13:00-14:00 | Lunch |
Programme Day 2 – Afternoon |
14:00-15:15 | Breakout Session 2: What don’t we know? Research Priorities for (i) industry (ii) other funders |
Each breakout group brainstorms the same question. Separate Moderators / Rapporteurs for each group.
30 minutes discussion followed by 45 minutes drafting RfP outline(s). |
Moderator: Alan Poole / Rapporteur: Nigel Gooderham
Moderator: Jorg Hackermüller / Rapporteur: Madeleine Laffont Moderator: Reza Rasoulpour / Rapporteur: Saskia van der Vies - Which answers are still needed? How can we provide the answers? - What is currently unsatisfactory about the use of ncRNAs? - What needs to change? - What are the priorities? - Complete outline RfP.
Complete RfP template(s) |
15:15-15:45 | Coffee |
15:45-16:30 | Plenary:
Moderators share RfP proposals & outcomes from Session 2. Room for audience participation. |
16:30 | Conclusions and Close Helmut Greim Munich Technical University, Germany |