Tag: #neuroblastoma

I’m Ronja

I’m Ronja, I’m from Germany, but have spent my entire adult life in the English-speaking parts of this world. Right after school, I interned with a PhD student working on cystic fibrosis for a couple of months. Having the chance to culture airway epithelial cells myself made me certain I was on the right track with biomedical sciences. So, I studied Biomedical Sciences (Anatomy) in Aberdeen. The best part of that degree was my introduction to dissections. I enjoyed them so much that I even considered becoming a full-time prosector. But that does not count as essential work, so I found a remote master’s degree in Health Research instead. Studying remotely gave me the fabulous opportunity to structure my own time. I could go and explore Scotland during the day and work in the evenings. But after 5 years of studying, I was finally ready to start a PhD and was ever so delighted when I heard I could weave in some dissections at RCSI. Now, I’m looking forward to discovering what Dublin has to offer and to getting stuck in my research project!

While I didn’t know much about the particulars of my PhD before starting, I had an idea about the project from the application and I knew accommodation was sorted out for me, but I had never seen the place or my future flatmates. The one thing that I was made aware of far in advance of moving to Dublin was that September was Child Cancer Awareness Month, for which the team was going to do a charity event. Based on past years I was expecting it to be a 10km run, which was pretty daunting to me. So, I prepared. I started running and cycling over the summer until 10km weren’t an issue anymore. But in the first lab meeting plans shifted. We were going to do the Dublin Mountains Way in a day. The 10km were tripled and depending on donations maybe even quadrupled. Quite a different challenge! But I believe my summer prepared me well for that too. Alongside running I started cycling a little as well. And because there was a free bike in Aberdeen for me, I cycled it down to Stirling. Let’s hope that the endurance needed to cycle 200km translate to hiking 30-42km!

Ronja Struck

Dublin Mountain Way in A Day, September 25th 2021

Here are our plans. This year we have upped the challenge, taking on the Dublin Mountain’s Way in a Day ⛰ We will hike through the Dublin Mountains from Tallaght to Glencullen, and maybe even all the way to Shankill on September 25th! Our challenge is not only to do #DMW in a Day & support three wonderful charities CMRF Crumlin/National Children’s Research Centre, Neuroblastoma UK and the Conor Foley Neuroblastoma Cancer Research Foundation but also beat our past fundraising records! If we raise 2K+, we’ll do 30km in a day. If 3K+ then 42km! Can u challenge us?  All funds raised will go to the 3 selected charities. Every donation big or small is hugely appreciated!

Please support us by donating to our Gofundme

https://gofund.me/ec59f131

Childhood Cancer Awareness Month 2021

Every 100th cancer patient is a child. Cancer is the 2nd most common cause of death among children after accidents. 

Childhood cancer is an umbrella term for many other types of this disease. Every September, many charities, researchers and parents of children with cancer work hard to raise awareness of this cancer. You may learn more about kids with cancer, their loving families, the doctors and caregivers who looking after them and treating them, the young survivors of cancer and those kids and teens who lost their battle, and the scientists who working hard to find a way to stop childhood cancer.

This year our research team will hike Dublin Mountain Way in One Day on the 25th of September 2021 whatever the weather in honour of Childhood Cancer Awareness Month. For every one euro donated to research only 1 cent of this goes to ALL childhood health conditions including cancer. Therefore, the donations we receive will be split equally among some wonderful children’s charities. These charities include the Conor Foley Neuroblastoma Research Foundation (CFNRF), Neuroblastoma UK (NBUK), Children’s Research & Medical Foundation (CRMF) Crumlin.

If you would like to get involved in this amazing challenge and help us raise vital funds for childhood cancers, you can contribute to our fundraising page:

A warm welcome to our new PhD students!

A warm welcome to our new PhD students Ronja and Erin! Both received the prestigious Irish Research Council – Enterprise Partnership Scheme Award. Indeed, I am a proud PI. This competitive scheme brings the most promising researchers to advance our knowledge across many disciplines, e.g. Law, Astronomy, Sociology, Biomedical Sciences and many more. A key element of this scheme is to work together with an Enterprise Partner.

We will work closely with the Conor Foley Neuroblastoma Cancer Research Foundation – a research charity led by the family who lost their child to neuroblastoma. An inspirational example of never giving up.

We will continue to dissect neuroblastoma biology using innovative platforms such as tumour-on-chip and 3D scaffold-based models in collaboration with our colleagues in the Tissue Engineering Research Group at RCSI and the Fraunhofer Project Centre at DCU.

This announcement is timely to celebrate Childhood Cancer Awareness Month in September.

Two talented and dedicated young scientists are joining our team. In 4 years time, we will have another pic of their graduation on the same stairs.

Upwards and onwards!!

Remote Research Projects

Regardless COVID19 pandemic, we continue to host undergraduate students from various Universities for their research projects. Two students, Carla and Chris, from the Technical University of Dublin, carried out BSc projects remotely. Having in-house datasets and many more published in open access, their projects were focused on bioinformatics, re-analysing them and giving a second look. Both Carla’s and Chris’ research received the highest score in their classes. Many congratulations – well deserved!! We wish to thank both for their kind words and willingness to share their story.

Chris Sheridan, the final year student in Biomolecular Science at the Technical University of Dublin, 2021

“My project concerned analysing the exosomal miRNA expression of neuroblastoma cells in response to chemotherapy. Though the project was not too large, it certainly was the largest project I have ever taken part in. The work Dr. Piskareva and her team are conducting is so interesting and novel that I felt very fortunate to be participating in such an exciting field. Despite the novel and complex nature of the topic, the project was extremely engaging, allowing for an opportunity to learn new valuable research and data analysis skills. I was able to get very useful and helpful feedback regularly from everyone on the research team, where there was a very welcoming and positive attitude. This made the topic seem less daunting and my goals more achievable. I was really happy with my results, and I am excited to see where they may lead in the future. Some of the miRNAs identified in the analysis may represent potential biomarkers or therapeutic targets for high-risk neuroblastoma patients. As I have yet to experience any lab-based research, it was cool to see the team’s approaches and applications of lab techniques and analysis strategies to see how research is conducted in the “Real World” after seeing these topics before only in lecture notes. Overall, the project was challenging but very rewarding and enjoyable. Throughout the project, the overall experience, the excitement of the results coming together, and the realisation that I may have something to contribute to this field of research cemented the idea in me that this is certainly the path I wish to pursue in science and for that, I would like to thank Dr. Piskareva and her team for such a positive and educational experience during my time with them.“

Carla Tejeda Monné, the final year Technological University of Dublin Biomolecular Science Student, specialising in Biotechnology, Therapeutics, and Drug Development, 2021

“During my final year project, I had the unique and amazing opportunity to work under the supervision of Dr. Olga Piskareva. The purpose of my thesis was to assess the clinical significance of Tumour Necrosis Factor Receptor Superfamily Member 1B and Member 4 (TNFRSF1B and TNFRSF4) in neuroblastoma patients. I accomplished this by analysing the gene profiles of several tumours using bioinformatic tools. In addition, I investigated the potential of microRNAs as therapeutic agents for neuroblastoma treatment. I thoroughly enjoyed carrying out this research project, and I hope the findings from my thesis can aid future research into the pathogenesis of neuroblastoma and the development of effective treatments for these children.“

Best of luck to Chris and Carla in their next endeavour!

In the Spotlight at EACR Virtual Congress

In early April, shortly after attending the Irish Association for Cancer Research (IACR) virtual conference, I was delighted to find out I had been selected for a “Poster in the Spotlight” presentation at the European congress in June. I was invited to give a 10-minute presentation about my research on finding new immuno markers for drug-resistant neuroblastoma. This would be my first time presenting at a conference outside of Ireland (though I remained in my home in Dublin and not in the hoped destination of Turino) and so it was a very exciting experience!

On the morning of my talk, I logged onto zoom to meet the EACR session organisers and the other speakers in my session – a mixture of PhD students and Post-doc researchers from Germany, Spain, Italy and the UK. Each of our talks was then broadcasted to the virtual congress platform where cancer researchers around Europe could tune in.

After the presentations, we joined a “Meet the Speakers” session where we could chat with those who had tuned in, answer questions and open up some research discussions. I was asked one question from a researcher doing similar work to me on how I investigate the relationships between certain genes in cancer, and I was able to refer her onto the software I use – I hope this aids her research, as that’s the real aim of attending these conferences!

Following this, it was time to relax and watch some of the other interesting talks taking place in the congress. The EACR were running a photo competition to show where you were watching from in order to win a place at the 2022 congress in Seville. So, I took this opportunity to take my laptop out to the back garden and watch the congress in the sun, getting a selfie for twitter with #NotQuiteTorinoEACR2021. Fingers crossed by this time next year travelling for international conferences will be a reality for researchers once again!

Catherine Murphy, Neuroblastoma UK funded PhD student

Sparkles of A Researcher Day

Once I mentioned the importance of the publication track record for a career in science. My team has been productive despite the COVID pandemic. Two review articles were published.

The first was a review written by Tom and published in Cancers focusing on the small extracellular vesicles produced by cancer cells that can transfer various growth signals to the tumour microenvironment aka neighbourhood and promote tumour expansion. The signal in focus was a protein called epidermal growth factor receptor (EGFR). It contributes to the healthy fitness of many different cells in the body. However, many cancer cells produce an excess of this protein giving them an advantage of growth over normal cells. Increased EGFR can be seen in breast, lung, glioblastoma and head and neck cancers.

Cancers 2020, 12(11), 3200; https://doi.org/10.3390/cancers12113200

The second review has been published in Journal of Personalized Medicine on March, 16th. Originally, it was a small review project for Nadiya, a medicine student, last summer. However, it became a big one with all data systematically collected, analysed and condensed. The focus of this review was on Retinoic Acid (RA), widely known as Vitamin A and its role in neuroblastoma. RA plays a vital role in human development. The main feature of RA is to push neuroblastoma cells to become neuron-like cell stopping their aggressiveness and cancer fate. So, we wanted to know more about the ongoing research both in the labs and the clinic. We reviewed primary research articles reporting basic and translational findings as well as clinical trials. Hopefully, it would help other researchers to get a full picture of this topic and a structured resource of experimental models and drugs tested.

J. Pers. Med. 2021, 11(3), 211; https://doi.org/10.3390/jpm11030211

International Childhood Cancer Awareness Day 2021

Every year, we celebrate Childhood Cancer Awareness Day Internationally. Pre-COVID times, it was straightforward to do a coffee morning, a bake sale, or as we did a Hot Chocholate morning.

To be honest with you, I had almost no presence of childhood cancer in my life until I joined Prof Stallings lab in 2011. When I said ‘almost’, I meant during my adulthood.

My Dad had a younger brother, both started their families at the same time. Our families used to spend a good time together, holidays, birthdays and weekends together. Both I and my cousin Igor were born almost within a year. I remember our play days together but at the level of feelings and stories told by my parents. In the pic, we were held by my nanna.

I do not have a pic where we were 3- or 4-years old. No pic was taken after Igor was diagnosed with blood cancer. He was 1-1.5-year-old. He travelled 800km to the best paediatric oncologists to receive the most progressive treatment back then. It extended his time with the family by four years. But he lost his battle…

How much can remember a 1-, 2-, 4- years old? My last memory – Igor was sleeping in a neat coffin. Adults were muttering. I remember, a tear slowly rolled down from Igor’s closed eyes. I naively asked my nanny why did the dead cousin cry??? He did not want to leave us, – said my nanny softly. 

Back then parents were not much informed on the disease, treatments, odds and alternative options. Igor was suffering, no pain relief options were available… No palliative care… Remember my nanny’s words: “These doctors had no hearts. All this child needed was a sense of peace, quiet time with his parents away from the hospital wards”. 

Many things have changed since then. Eight out of 10 children with blood cancer are responding to treatment well, they reach adulthood, may even have kids of their own. However, there are some types of childhood cancers that do not respond well and can return to being more aggressive. Cancer steals the child’s future. One of the thieves is neuroblastoma, a solid tumour of undeveloped nerves.

Childhood cancer research is essential to return happy days to kids and their families. Many childhood cancer research charities do their best to secure funds and support researchers like me. It is vital to have a continuous investment in research that helps to understand the weakness of childhood cancer and develop new drugs designed exclusively for kids.

Today I want to thank 3 charities for their hard work: Children’s Health Foundation Crumlin, Neuroblastoma UK and the Conor Foley Neuroblastoma Cancer Research Foundation. And ask you, my readers, to donate to a childhood cancer charity of your choice.

How neuroblastoma cells spread?

Since I joined neuroblastoma research, I have been puzzled by the fact that half of the children with neuroblastoma have the disease spread at the time of diagnosis. It is still a puzzle whether cells spread and primary tumour growth happen simultaneously or more adventurous cancer cells escape the primary tumour location later.

At a cancer conference, I met Prof Ewald who studies this process in breast cancer. I was fascinated by the approach and started to look for opportunities to join his lab. To tell the truth, very few exist for mid-stage career scientists! One of them is the Fulbright program.

One day, I opened my email saying that I received a Fulbright-HRB Health Impact Scholar Award to travel to Johns Hopkins University and adapt their 3D models to learn how neuroblastoma spreads. It was a life-changing experience both personally and professionally. The amount of experimental data collected over 4 months of work did not fit a 1TB memory stick! Indeed, this short journey was just a start of a new research inquiry.

On my return home, the greatest task that remained was to make sense of every single experiment. Cian Gavin took over and spent almost a year systematising, characterising it, and placing it into a context. It was meticulous work with very little known about invasion strategies in neuroblastoma. Now, we are happy to share our findings published on Cancers.

Where do we go now? Well, our next step is to understand the cellular players behind neuroblastoma invasion and how we can target them to stop neuroblastoma spread. It won’t be a short and sweet journey, but we are ready for it!

This fantastic and rewarding work was supported by Fulbright Commission Ireland, National Children’s Research Centre, Health Research Board, Science Foundation Ireland, the National Institutes of Health/National Cancer Institute (Prof Ewald), Alex’s Lemonade Stand Foundation for the COG Childhood Cancer Repository (Prof Reynolds) and the National Institutes of Health/National Cancer Institute (Prof Reynolds).