Exciting times ahead for my team – to study neuroblastoma – immune cells interaction. This 3 years project is funded by Neuroblastoma UK to support the interdisciplinary collaboration between experts in fields of neuroblastoma biology, immunology and tissue engineering from Royal College of Surgeons in Ireland, Trinity College Dublin and Queen Mary University London.
Catherine will grow different neuroblastoma cells together with immune cells using a 3D printing technology. She will travel to Queen Mary University London and learn how to do 3D tumour bioprinting. This technology allows the generation of reproducible scaffolds that replicate the architecture of tumour tissues as seen in patients. She will use RCSI/AMBER facilities to optimise this model here and to study how immune cells recognise cancer cells, attack and eventually kill them. This experimental model will help us to advance current immunotherapies and develop more effective treatments for neuroblastoma.
Here, we are – the Irish neuroblastoma research team landed at the 5th Neuroblastoma Research Symposium in Cambridge. Four poster presentations by four enthusiastic scientists. The two days crash course in neuroblastoma – vibrant, intense, informative.
I had one of the most enjoyable poster sessions in the last few years! A genuine interest in our 3D in vitro cancer models by both academics and Industry. Hope, to keep the ball rolling and strengthen these new links.
The Symposium programme was an excellent balance of the new transnational outcomes with hardcore developmental cellular programmes. From ‘How neuronal precursors select their fate and how they can escape the developmental constraints? How this knowledge can help to advance our understanding of neuroblastoma aetiology?’ to ‘New drugs that demonstrated great potency in pre-clinical studies’ via ‘how we can work together more efficiently to progress quicker’
Indeed, the success of the research meeting became possible thanks to the strategic vision and leadership of organisers!
13:00 – 13:10 Introduction – Neuroblastoma UK & CRUK Cambridge Centre
Session 1: Neuroblastoma biology & prognosis
Cancer Research UK Cambridge Centre Neuro-oncology Programme Session
Chair: Kate Wheeler (Oxford Children’s Hospital)
13:10 – 13:40 Sandra Ackermann (Cologne): The genetic basis of favourable outcome and fatal tumour progression in neuroblastoma
13:40 – 14:10 Rogier Versteeg (Amsterdam): The dark side of neuroblastoma
14:10 – 14:40 Katleen de Preter (Ghent): Improved diagnosis and risk stratification of paediatric cancers using liquid biopsies
14:40 – 14:55 Sue Burchill (Leeds): Self-renewing neuroblastoma cells isolated from bone marrow aspirates of children with stage M disease share a mesenchymal expression signature: an NCRI CCL CSG Neuroblastoma Group Study
14:55 – 15:15 Combined discussion
15:15 – 15:45 Tea with Posters
Session 2: Targeted & combination therapy I
Cancer Research UK Cambridge Centre Neuro-oncology Programme Session
Chair: Marie Arsenian Henriksson (Karolinska)
15:45 – 16:15 Frank Westermann (Heidelberg): Novel metabolic dependencies of MYCN-driven neuroblastoma
16:15 – 16:45 Gerard Evan (Cambridge): Is Myc really master of the universe?
16:45 – 17:00 Melinda Halasz (University College Dublin): Anti-Cancer Effects of Diphenyleneiodonium Chloride (DPI) In MYCN-Amplified Neuroblastoma
17:00 – 17:15 Evon Poon (ICR, Sutton): Pharmacological blockade of high-risk MYCN driven neuroblastoma using an orally-bioavailable CDK2/9 inhibitor
17:15 – 17:35 Combined discussion
Downing College – Main Hall.jpg
17:35 – 19:15 Poster viewing & Drinks
19:30 Symposium Dinner at Downing College (map for dinner)
FRIDAY 12TH APRIL 08:30 – 08:50 Coffee & pastries
Session 3: Neural crest & differentiation therapy I
Chair: Margareta Wilhelm (Karolinska)
08:50 – 09:20 Igor Adameyko (Karolinska): Normal development of sympathoadrenal system resolved with lineage tracing and single cell transcriptomics
09:20 – 09:50 Quenten Schwarz (Adelaide): Guiding sympathoadrenal neural crest cells to the adrenal primordia
09:50 – 10:05 Claudia Linker (King’s College London): Notch coordinates cell cycle progression and migratory behaviour leading to collective cell migration
10:05 – 10:20 Combined discussion
10:20 – 10:50 Coffee with Posters
Session 4: Neural crest & differentiation therapy II
Chair: Gareth Evans (York)
10:50 – 11:20 Karen Liu (King’s College London): ALK and GSK3 – shared features of neuroblastoma and neural crest
11:20 – 11:35 Anestis Tsakiridis (Sheffield): Efficient generation of trunk neural crest and sympathetic neurons from human pluripotent stem cells via a neuromesodermal progenitor intermediate
11:35 – 12:05 Anna Philpott (Cambridge): Using developmental mechanisms to drive differentiation of neuroblastoma
12:05 – 12:20 Combined discussion
12:20 – 13:20 Lunch with Posters
Session 5: Targeted & combination therapy II
Chair: Bengt Hallberg (Gothenburg)
Cancer Research UK Cambridge Centre Paediatrics Programme Lecture:
13:20 – 13:50 Sharon Diskin (Philadelphia): A multi-omic surfaceome study identifies DLK1 as a candidate oncoprotein and immunotherapeutic target in neuroblastoma
13:50 – 14:05 Donne Nile (Glasgow): Manipulation of cancer cell metabolism for neuroblastoma combination therapy with targeted radiotherapy
14:05 – 14:35 Suzanne Turner (Cambridge): CRISPR-dCas9 screens to identify resistance mechanisms to ALK in neuroblastoma
14:35 – 14:50 Combined discussion
14:50 – 15:20 Tea with Posters
15:20 – 15:30 Poster prizes
Session 6: Targeted & combination therapy III
Chair: John Lunec (Newcastle)
15:30 – 16:00 Per Kogner (Karolinska): The PPM1D encoded WIP1 phosphatase is an oncogene significant for cancer development and tumour progression and a druggable therapy target in neuroblastoma and medulloblastoma. A hint as to how aggressive childhood cancer manages with wild-type p53
16:00 – 16:15 Deb Tweddle (Newcastle): Preclinical assessment of MDM2/p53, ALK and MEK inhibitor combinations in neuroblastoma
16:15 – 16:30 Sally George (ICR, Sutton): A CRISPR-Cas9 genomic editing and compound screening approach identifies therapeutic vulnerabilities in the DNA damage response for the treatment of ATRX mutant neuroblastoma
16:30 – 16:45 Miriam Rosenberg (Jerusalem): Expression- and immune-profiling of neuroblastoma-associated Opsoclonus Myoclonus Ataxia Syndrome (OMAS) to identify features of auto- and tumour-immunity
Our team has expanded. Now, we are 11 – a great mix of cultures and science backgrounds! But it comes at a price – how to agree on even simple activities? Shall we go hiking? Bowling? Karting? Room Escape?
Poll it! Vualá,and the leader is Pizza Making Party!
Across countries and continents, we are celebrating International Childhood Cancer Day (ICCD).We do it to raise awareness tto raise awareness of childhood cancer, its consequences for children and their parents and make it as a priority for Governments and research.
My team research is focused on neuroblastoma biology. This is a solid tumour of undeveloped nerves. Some forms of neuroblastoma spread quickly and become very aggressive and challenging to treat. We are searching for the weaknesses that can be targeted with drugs.
A guessing game was a part of the event. Everyone had a chance to guess how many marshmallows fitted in the cell culture flask T75. The guesses ranged from as low as 95 to as high as 500. Fortunately, one of the participants gave an absolutely correct answer. Micheal Flood put on 173 and won. Her fantastic ability to guess is incredible! Congratulations!!! Well done to all!
We raised 698.91 Euros for childhood cancer research! We thank everyone who came along and supported the Hot Chocolate Morning & the International Childhood Cancer Day 2019!
Many special thanks go to Amorino for delicious Italian hot chocolate & tasty bites contributors!
International Childhood Cancer Day (ICCD) was founded in 2002 by Childhood Cancer International (CCI). Each year on February 15th we unite together to recognise childhood cancer as a national and global child health priority & to raise support, funding and awareness of this devastating desiease.
This year we team up with Amorino to run Hot Chocolate Morning. Please come along! All proceeds go to CMRF/NCRC and CFNCRF.
Coming to live and work for a short period ignites opposite feelings. Should I see all the places recommended by Tripadvisor or do it at my pace as it happens? What if I miss something worthy? Perhaps, your own intuition balances somehow both.
I have discovered and loved two buildings in Baltimore. One is the building of Barnes & Noble bookstore in Inner Harbour and the other is Mount Vernon Place Church. Both have a great history behind and give a very warm feeling when you are inside.
Barnes & Noble bookstore is located in the former Power Plant. The features are easily spotted. From outside, the building looks like a Plant for modern social activities. Ugly slightly, isn’t it? Though, it is a different feeling when you enter the bookstore. The Plant scaffolds, chimneys and pipes are nicely crafted into a warm welcoming environment. Even lights are dimmed as back then. Rambling through the bookshelves and feeling the magic of the place and unread stories on them. You can pick up a book, sit where you are and enjoy the reading. Maybe it is the feeling of my childhood full of books and hours of reading?
Mount Vernon Place Church
Mount Vernon Place Church is next to the Washington Monument and recalls old Catholic Cathedrals in a Victorian Gothic Style. Built in 1872, the Church is actually the United Methodist Church from the very beginning. It is beautiful inside as well as outside. The stained glass and carvings have Nature themes. A big rose window in the rear of the church was inspired by the one in Notre Dame. It has an interesting history which you can read here. I discovered this place by chance and am glad that this chance came from my host family. I saw the interior not only the Church but also Asbury House. The mansion was a home to the first bishop of the Methodist Church in America – Francis Asbury (1745-1816). Have a look at the pictures, the furniture is well preserved, the staircase is similar to the one you can see in Slane Castle. Its light design makes it looks flying. Indeed, not everyone could use it at that times. Servants had a plain version at the back of the house, so none could have seen them moving in and out. Lots of blue and carved wood in the rooms. Incredibly beautiful.
What is a must-see in Ireland? Right: visit Guinness brewery at St. James’s Gate and have a pint of right Guinness. It is one of the most recognised and famous beer brands. Rumours say Dublin is the only place where Guinness tastes Guinness. Traditions, traditions and traditions. Though the one we like most Guinness Draught is a relatively new addition – it was introduced almost 200 years after the brewery establishment in 1759 by Arthur Guinness.
So, what if you like tastes ‘outside the box’? Then Guinness brewery in Baltimore is for you. Respecting the Father, they do completely different stuff. Imagine, 16 different tastes, including the one we know! You can have a guided tour of the brewery, hear the great story and do a beer tasting. Have you tried one? Not, the one in the pub or with the friends at BBQ. It is a special way to feel the bouquet of flavours and taste the difference. There is a difference between the beer drunk straight from the bottle and from the glass. Because you can smell it as simple as that.
Taste of Guinness, the Guinness Brewery opened in Baltimore, MD, the USA in 2017
During our guided tour, we rambled inside the experimental brewery, learn the basics of beer production, tasted 4 types of beer: Guinness Blonde, Oatmeal Pale Ale, Guinness Draught and Guinness Milk Stout. Three were absolutely new for me. I liked Oatmeal Pale Ale, found Milk Stout a bit dessert style, Blonde – too citrusy. Do not forget, another 12 you can taste at the bar in a special set! However, to enjoy the most you have to bring your friends. All is much better with the right company!
Can you control the time? I can’t and know none who can. It flies, when things around you work out, and drags on when not. The time flies for me here in Baltimore. It feels so intense sometimes and then slightly slows down. I take pictures almost of everything: the path’s signposts when rambling in the network of Johns Hopkins Buildings, the first frosty morning, joyful deer at the backyard of my host family house, outdated clothes in the shop…
In the past, I had a similar journey to Ireland. It was 3 months research placement during my PhD. Did I like it – oh, yes I did! I travelled a lot, felt romantic and changed my life on my return home. But I did not run a diary or tag my way on Facebook. I have learnt the lesson: do it even more intense as you can’t travel back in time and write down your experience. It may be funny or educational to read in a couple of years! I become addicted to it though not always have time to do it.
I like the people who I am working with. They are a fantastic bunch of self-motivators and open-minded personalities. They are workaholics either naturally like me or because of the exciting projects they do like I do. Who knows, but very likely because of both. Isn’t it a dream to have an exciting project and great people around you? The luck like this gives you wings.
The American enthusiast studying Russian and my Mum
The host family – is my other great luck! This luck was crafted as a parallel story when none knew how the Fulbright application and an American enthusiast learning Russian may intersect. You would not believe, but parallel lines can be non-parallel sometimes! His journey to my home city in Russia paved the way to the opportunity to stay at his aunt’s house.
Every day 50 min drive to and from Hopkins opens up the other side of the local lifestyle and infrastructure. What are the rush hours? How many drivers are signalling before taking a turn? How do they call the shopping trolley? How parking system works?
Experiencing life as an American working in Baltimore.
This is how my journey began. On Tuesday, I received an invite from the Children’s Medical Research Foundation to attend the Annual Summer Gala Dinner at the Water Club in Manhattan on Thursday the same week. Are two days enough to plan your trip? Perhaps it depends on many things, I had no reservations. The only one uncertainty was car parking logistics.
Those, who are familiar with Baltimore history and current life, know that your car is your Castle. After the Internet search and chats with my host family, the plan was to get a bus to NY which provides a designated car park.
Three hours on the bus flew in a flash. Wide roads with trees on both sides did remind me of some motorways in Russia. Gigantic tolls – almost 12 lanes in both directions. An impressive tunnel under the Hudson River connects the mainland with Manhatten. One can see a borderline dividing the tunnel into New Jersey and New York parts on about halfway.
What was my first impression of NY once I got off the bus? Many snapshots instantly jumped in linking with Hollywood movies that pictured NY. Mostly from ‘Sex and the City’. A traffic jam here and there. Crazy Taxi and car drivers. Brainless pedestrians. Everyone on the run. Madness. I did enjoy it as a tourist. Would I cope with it on everyday bases? A very big question!
Unfortunately, thanks to the hurricane Florence, not much sightseeing was on offer. All tall buildings were hidden with clouds. Tourists were queuing for hop-on-off.
I had 2 hours before the bus to Baltimore. My choice was Times Square. A classical picture – huge screens are talking to you offering pleasure and entertainment. Come in, relax and enjoy!
Strolling around Cafe shops, theaters, food vans. Looking at tourists and locals. Feeling and absorbing… Short, but sweet.