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Biography

Wei Wu received her PhD from the National University of òòò½Íøin 2014 with dual-training in cancer biology and mass spectrometry (MS). In this period, she was supported by the President’s Graduate Fellowship and was the recipient of three international Young Investigator Awards in Berlin, Yokohama and Beijing, each time showcasing her ability to combine MS technologies with the pursuit of mechanisms in cancer biology. During her postdoc in the Netherlands with world renowned protein scientist Albert Heck, Wei developed diverse and sensitive affinity tools to measure signaling in the tumor micro-environment (TME), and became interested in paracrine impacts mediated through secretion and cell-cell contact. In 2017, she started her group in Utrecht University with a niche in cancer antigen discovery and TME crosstalk, focusing on the extracellular factors needed for immunosurveillance and T cell function. In this period, her extensive collaborations with Dutch scientists in tumor immunology only intensified her interest, in providing mechanistic resolution and technological solutions, towards better immunotherapy and pre-emptive intervention. Since 2021, Wei served as a nominated representative from central Europe in the world Human Proteome Organisation (HUPO) council, and was appointed to the international executive committee of the HUPO Human Immuno-Peptidome Project (HUPO-HIPP). In 2022, she moved back to òòò½Íøto join A*STAR-SIgN, focusing on cancer antigen targeting and understanding tissue microenvironmental crosstalk.

Affiliations

• Associate Professor, Department of Pharmacy, National University of òòò½Íø(joint appointment)
• Associate Professor, Department of Pharmaceutical Sciences, Utrecht University, The Netherlands (visiting)

Research Focus

Cancer antigen targeting
The lab focuses on identification of novel tumor-surface signatures that may be exploited for immunotherapy.

In a three-pronged approach, the goal is to target tumor vulnerabilities and dependencies in antigen presentation, membrane proteins and cell-surface protein-protein interactions, to engineer novel immuno-therapeutic routes.



By applying hypothesis-free mass spectrometry discovery in novel model systems, recent findings include:

• ,  and  in antigen presentation (JPR, 2021; MCP, 2021; JPR, 2019)
• and  (Nat Comm, 2020; Front Immunol, 2021)
• (Comm Biol, 2021)
• and  (Nature, 2017; Cell reports 2021)
• (Mol Immunol, 2021)

Tissue microenvironmental crosstalk
Crosstalk between different cell types in the tissue microenvironment is critical in health and disease. The complexity in inter-cellular signaling depends on a myriad of long- and short-range communication channels that may be contact dependent or independent.

By coupling novel affinity tools with ultra-sensitive innovations in mass spectrometry, the goal is to dissect the paracrine influence of different cell types during normal tissue homeostasis, and sustenance of a malignant tumor niche.

Through hypothesis-free screening of secreted cytokines, extracellular vesicles and extracellular matrix components, recent tools and findings in physiology and crosstalk include:

• (Nat Comm, 2020)
• and enzyme specificities (Cell, 2020)
• (MCP, 2018)
• (Comm Biol, 2019)
• Immuno-suppressive TME in neuroblastoma

Lab Members

Publications

Publications_Wei Wu (last updated 26 February 2025)