Grant Details
| Grant Number: |
1OT2CA321158-01 Interpret this number |
| Primary Investigator: |
Weissman, Jonathan |
| Organization: |
Whitehead Institute For Biomedical Res |
| Project Title: |
Project Illumine - Exploiting the Dark Proteome to Fight Cancer |
| Fiscal Year: |
2026 |
Abstract
ABSTRACT
Cells produce a previously under-appreciated class of non-standard proteins collectively termed the
dark proteome that are not encoded by known open reading frames or explained by DNA mutations.
The biological origins, regulation and functional role of the dark proteome in normal tissues and
cancer remains largely unknown. This challenge aims to uncover the mechanisms that give rise to
dark proteome products and to define their connection to the oncogenic state. Team ILLUMINE led
by Reuven Agami (Netherlands Cancer Institute) brings together interdisciplinary researchers with
expertise in cancer biology, proteomics, genomics, chemistry, technology development and clinical
translation. The program will address four central questions: who the dark proteome players are,
whether and how they are (dys)regulated in cancer, how they function, and how they can be
therapeutically exploited. In addressing these questions, ILLUMINE will address major gaps in
knowledge. Aim 1 will create a comprehensive map of dark proteome entities across several major
cancer types and dissect potential stress-related mechanisms for their production. Aim 2 will codify a
bench-to-bedside pre-clinical therapeutic development pipeline for immunotherapies from the dark
proteome. Aim 3 will profile cell-based mechanisms of individual dark proteins in cancer biology,
focusing on cell autonomous and non-cell autonomous mechanisms. Aim 4 will explore non-
immunotherapy opportunities for targeting the dark proteome. Capitalizing on its unique expertise the
team plans to use and combine cutting-edge experimental approaches to uncover hidden layers of
cancer cell biology. ILLUMINE aims to ultimately identify new tumor biology and treatment paradigms
for patients based on the dark proteome.
Publications
None