TY - JOUR
T1 - Cancer proteogenomics
T2 - current impact and future prospects
AU - Mani, D. R.
AU - Krug, Karsten
AU - Zhang, Bing
AU - Satpathy, Shankha
AU - Clauser, Karl R.
AU - Ding, Li
AU - Ellis, Matthew
AU - Gillette, Michael A.
AU - Carr, Steven A.
N1 - Publisher Copyright:
© 2022, Springer Nature Limited.
PY - 2022/5
Y1 - 2022/5
N2 - Genomic analyses in cancer have been enormously impactful, leading to the identification of driver mutations and development of targeted therapies. But the functions of the vast majority of somatic mutations and copy number variants in tumours remain unknown, and the causes of resistance to targeted therapies and methods to overcome them are poorly defined. Recent improvements in mass spectrometry-based proteomics now enable direct examination of the consequences of genomic aberrations, providing deep and quantitative characterization of tumour tissues. Integration of proteins and their post-translational modifications with genomic, epigenomic and transcriptomic data constitutes the new field of proteogenomics, and is already leading to new biological and diagnostic knowledge with the potential to improve our understanding of malignant transformation and therapeutic outcomes. In this Review we describe recent developments in proteogenomics and key findings from the proteogenomic analysis of a wide range of cancers. Considerations relevant to the selection and use of samples for proteogenomics and the current technologies used to generate, analyse and integrate proteomic with genomic data are described. Applications of proteogenomics in translational studies and immuno-oncology are rapidly emerging, and the prospect for their full integration into therapeutic trials and clinical care seems bright.
AB - Genomic analyses in cancer have been enormously impactful, leading to the identification of driver mutations and development of targeted therapies. But the functions of the vast majority of somatic mutations and copy number variants in tumours remain unknown, and the causes of resistance to targeted therapies and methods to overcome them are poorly defined. Recent improvements in mass spectrometry-based proteomics now enable direct examination of the consequences of genomic aberrations, providing deep and quantitative characterization of tumour tissues. Integration of proteins and their post-translational modifications with genomic, epigenomic and transcriptomic data constitutes the new field of proteogenomics, and is already leading to new biological and diagnostic knowledge with the potential to improve our understanding of malignant transformation and therapeutic outcomes. In this Review we describe recent developments in proteogenomics and key findings from the proteogenomic analysis of a wide range of cancers. Considerations relevant to the selection and use of samples for proteogenomics and the current technologies used to generate, analyse and integrate proteomic with genomic data are described. Applications of proteogenomics in translational studies and immuno-oncology are rapidly emerging, and the prospect for their full integration into therapeutic trials and clinical care seems bright.
UR - http://www.scopus.com/inward/record.url?scp=85125538569&partnerID=8YFLogxK
U2 - 10.1038/s41568-022-00446-5
DO - 10.1038/s41568-022-00446-5
M3 - Review article
C2 - 35236940
AN - SCOPUS:85125538569
SN - 1474-175X
VL - 22
SP - 298
EP - 313
JO - Nature Reviews Cancer
JF - Nature Reviews Cancer
IS - 5
ER -