Peter Campbell
彼得·坎贝尔
MB BChir, PhD, FMedSci
Head of Cancer, Ageing and Somatic Mutation Programme癌症、衰老与体细胞突变项目负责人
👥Biography 个人简介
Peter Campbell FMedSci is Head of the Cancer, Ageing and Somatic Mutation Programme at the Wellcome Sanger Institute and a Professor at the University of Cambridge. He is one of the world's leading cancer genomicists, with foundational contributions to the Pan-Cancer Analysis of Whole Genomes (PCAWG) consortium and to the COSMIC database of somatic mutations in cancer. His laboratory pioneered the systematic classification of mutational signatures (SBS, DBS, ID classes) using non-negative matrix factorization, establishing the COSMIC signatures catalogue now used globally in cancer genomics research and clinical diagnostics. Campbell's work on clonal haematopoiesis revealed how somatic mutations accumulate in ageing blood stem cells and predispose to haematological malignancies. His group also performed landmark whole-genome sequencing studies of acute myeloid leukaemia, myeloproliferative neoplasms, and multiple myeloma, uncovering driver mutation landscapes and evolutionary trajectories. He has led major international collaborative studies through ICGC and PCAWG, and his algorithms for driver gene discovery and signature extraction (SigProfiler) are standard tools in the field. Campbell is a Fellow of the Academy of Medical Sciences and recipient of numerous honours including the AACR Award for Outstanding Achievement in Cancer Research.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
Mutational Signatures (COSMIC Catalogue)
Led the systematic extraction and annotation of single-base substitution (SBS), doublet-base substitution (DBS), and indel (ID) mutational signatures from thousands of cancer whole-genome sequences, establishing the COSMIC signatures catalogue that is the international reference for understanding mutagenic processes in cancer.
Pan-Cancer Analysis of Whole Genomes (PCAWG)
Co-led the PCAWG consortium analysis of 2,658 whole cancer genomes across 38 tumour types, producing landmark papers in Nature (2020) that redefined the landscape of non-coding driver mutations, structural variants, and mutational processes in human cancers.
Clonal Haematopoiesis and Ageing
Demonstrated that somatic mutations in haematopoietic stem cells accumulate with age and that clones carrying DNMT3A, TET2, and ASXL1 mutations expand progressively, establishing clonal haematopoiesis of indeterminate potential (CHIP) as a risk factor for haematological malignancy and cardiovascular disease.
Cancer Evolutionary Dynamics
Developed computational frameworks for reconstructing the evolutionary history of tumours from sequencing data, revealing punctuated versus gradual modes of cancer evolution and informing understanding of treatment resistance and metastatic spread.
Representative Works 代表性著作
The repertoire of mutational signatures in human cancer
Nature (2020)
Comprehensive analysis of 84 million somatic mutations from PCAWG cohort defining 49 SBS, 11 DBS, and 17 ID signatures and attributing them to known and novel mutagenic processes.
Pan-cancer analysis of whole genomes
Nature (2020)
Flagship PCAWG paper reporting the landscape of driver mutations, non-coding alterations, and tumour evolutionary patterns across 38 cancer types from 2,658 whole genomes.
Age-related clonal haematopoiesis associated with adverse outcomes
New England Journal of Medicine (2014)
Landmark study linking age-associated somatic mutations in blood stem cells to increased risk of haematological cancer and all-cause mortality.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-01-15 | All information from publicly available academic sources
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