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Postdoc - Trace the cellular origin of neuroblastoma relapse

A postdoc position is available at the department of Oncogenomics, Amsterdam UMC, to study mechanisms of therapy resistance and development of relapse in the pediatric tumor neuroblastoma.
Postdoc - Trace the cellular origin of neuroblastoma relapse
Vragen?
Solliciteer direct
  • Aantal uur: 36 uur per week
  • Specialisme: AMC Medical Research B.V.
  • Contractvorm: bepaalde tijd
  • Salaris: € 2.911 - € 4.615
  • Reageer tot en met: 21 december 2021
Solliciteer direct Reageer binnen 17 dag(en)
Wat ga je doen?

We have established that neuroblastoma is composed of two phenotypically divergent types of tumor cells (van Groningen et al., Nat Genet., 2017. PMID 28650485). An undifferentiated, mesenchymal tumor cell-type is resistant to therapy and we hypothesize that these cells are responsible for the outgrowth of relapse tumors. In a KWF-funded project, we aim to rigorously test this model using genetic lineage tracing of the divergent neuroblastoma cell types in relapse models of human neuroblastoma.
You will be responsible for the development and validation of lineage-tracer cell lines, which includes the molecular cloning of targeting vectors and CRISPR/Cas9-mediated targeted integration in neuroblastoma cell lines. These lineage-tracing cell lines will be tested in neuroblastoma xenograft models of relapse development. You will analyze lineage-traced cells using single-cell RNA sequencing to study transcriptional plasticity during the development of relapse.

Vragen over deze functie?
Tanja Hart Tanja Hart +31621603178 Recruitment adviseur
Over het project

Research in our laboratory is focused on the phenotypic heterogeneity and plasticity of cancer cell types to unravel the fundamental principles of neuroblastoma biology. We aim to identify the cell-of-origin of neuroblastoma relapse and understand the plasticity of cellular states in tumor progression and relapse development. The outcome of these studies will guide the development of new combination therapy to combat neuroblastoma.

Wat neem je mee?

Successful candidates have a PhD degree with a strong background in stem cell biology, developmental biology, and/or cancer research. Expertise with molecular cloning, cell culture, CRISPR/Cas9 targeting, and mouse xenograft models is required. Experience with single-cell RNA sequencing is advantageous. We look for an ambitious, independent scientist with a critical and analytical mind-set to develop this research line. Excellent English communication skills, both written and oral, are required.

Wat bieden we jou?
  • A full-time postdoc position is available for 2 years, with an evaluation after 1 year. Starting date is as soon as possible or after agreement.
  • Additional benefits include an 8.3% end-of-year bonus and 8.0% holiday pay.
  • The base salary does not include holiday pay (8%) and a year-end bonus (8.3%).
  • In addition to excellent accessibility by public transport, Amsterdam UMC (location AMC) also has a sufficient number of parking spaces for employees.
  • Pension is accrued at Be Frank.
Waar ga je werken?

You will work at the Department of Oncogenomics (Dr. Johan van Nes, Amsterdam UMC – location AMC). We collaborate with the bio-informatic team of Dr Jan Koster (Amsterdam UMC, r2.amc.nl) for genome-wide epigenetic analysis and transcriptional data at single-cell resolution. Live imaging-, cell sorting- and genome-analysis facilities at the Amsterdam UMC provide state-of-the-art technolgy and support for the in-depth analysis of lineage tracing data.

Wat kun je verwachten?
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For further information about the position, please contact dr. Johan van Nes by e-mail (w.j.vannes@amsterdamumc.nl) or phone (+31 (0)20 5667536).

For more information about the application procedure please contact Tanja Hart, Recruitment Adviser, via T: 06-21603178 or E: t.hart@amsterdamumc.nl

A reference check, screening and hiring test may be part of the procedure. Read hier whether this also applies to you. 

Acquisition in response to this vacancy is not appreciated.