Excited about when (childhood) #cancer and #developmental #biology converge, tumor initiation and #neuralcrest. Located at @lunduniversity, Sweden

Lund, Sverige
Joined May 2012
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Our new paper is out! 📣 ”Cell types or cell states? An investigation of adrenergic and mesenchymal phenotypes in neuroblastoma” cell.com/iscience/fulltext/S… Excellent work from @evo_eco_onco and @AnderssonStina_ ✨
Officially out in iScience now! Check it out here: cell.com/iscience/fulltext/S… Key take-away: differential proliferation and survival of adrenergic and mesenchymal phenotypes, rather than cell state switching, likely drives therapeutic response in neuroblastoma!
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Awesome science, awesome PI - apply! 🤩
Join our #SystemsImmunology Lab (Lund University, Sweden) as a #Postdoctoral Fellow! 🔬Investigate sex hormone regulation of human immune function using CRISPR, transcriptomics, and immunophenotyping. Fully funded 2-year position (more info attached). 🗓️Apply by Jan 6, 2025
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Join our #SystemsImmunology Lab (Lund University, Sweden) as a #Postdoctoral Fellow! 🔬Investigate sex hormone regulation of human immune function using CRISPR, transcriptomics, and immunophenotyping. Fully funded 2-year position (more info attached). 🗓️Apply by Jan 6, 2025
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The one and only - @adameykolab
🌟Last week, we wrapped up our 2024 #StemCellStars series with a talk by Prof. Igor Adameyko from @karolinskainst & @MedUni_Wien on clonal analysis in embryonic development using single-cell tech. Thanks to Prof. Adameyko, attendees & chair @hammarlund_emma! Stay tuned for 2025!
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Sofie Mohlin retweeted
Here's a chicken embryo after nine days of development. The polka dot pattern shows clusters of cells that will produce feathers 🐣🔬
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Tune in tomorrow!
Attend on Friday 25 October the Nordic #DevBio seminar series: Malin @ParmarLab Single cell omics - bringing better cell therapies to patients  & Sofie @mohlinlab Factors triggering cancer development during embryogenesis @lunduniversity Link: lu-se.zoom.us/j/61935143528
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Runner-up for best article of the year award! @Lund_Stem PhD student @elinafredlund did a fantastic job (as always!) presenting our work ✨ science.org/doi/10.1126/scia…
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Apply, apply, apply. You will join an amazing person and scientist!
PhD position alert 🚨 I am looking for 2 PhD students to join my group on cancer initiation at @StAnna_CCRI. #FWF funded project using human iPSC, origins and transcript omics. We have very supportive and collaborative environment in lively Vienna. Apply! ccri.at/working-at-the-ccri/…
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📰Researchers from the @mohlinlab at @lunduniversity have found that the gene MOXD1 is associated with a poorer prognosis in #neuroblastoma, a rare form of childhood cancer with a low survival rate. Read more about the discovery now in @ScienceAdvances ⤵️ stemcellcenter.lu.se/article…
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Polina is an amazing scientist and person - take the chance to join her road towards producing great science!
I work hard now to set up the lab at @StAnna_CCRI and start the research on #pediatric_cancer #initiation using #iPSC models. I am looking for the first team member - #lab_manager! Please apply and help to spread the word. lnkd.in/d9aqY8pn Job Openings - St. Anna CCRI
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Paper alert! 🔔 ✨ Read all about how trunk neural crest gene MOXD1 is a tumor suppressor in childhood cancer neuroblastoma, a specific marker for MES cells, and restricted to Schwann Cell Precursors during embryonic lineage specification @ScienceAdvances science.org/doi/10.1126/scia…
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It has been a long process (as publication always seems to be nowadays), where we split up our original submission (and bioRxiv version) in two - a cancer part and a development part. We had too much data according to reviewers 🤷🏼‍♀️
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Looking forward to get our part on MOXD1 during embryogenesis out, submission ongoing! Keep an eye out!
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Our findings suggest cell type-specific origin of neuroblastoma subtypes, and understanding the mechanism behind this tumor suppressor could help in identifying and treating this group of tumors.
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At last, MOXD1 is a specific marker of MES phenotype cells in neuroblastoma, and expression is restricted to Schwann Cell Precursors during trunk neural crest cell lineage specification.
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Using CRISPR-mediated knockout models of zebrafish and chorioallantoic membrane assays, as well as overexpression models of patient cells and mouse xenografts, we show that MOXD1 is a tumor suppressor gene in neuroblastoma.
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We show that loss of MOXD1 at 6q23 predicts extremely poor outcome in patients with high-risk disease. The prognostic information of MOXD1 expression is tumor-specific, and restricted to childhood cancer form neuroblastoma.
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