Quantitative Imaging in Cancer Evolution and Ecology
Open accessAbstract
Cancer therapy, even when highly targeted, typically fails because of the remarkable capacity of malignant cells to evolve effective adaptations. These evolutionary dynamics are both a cause and a consequence of cancer system heterogeneity at many scales, ranging from genetic properties of individual cells to large-scale imaging features. Tumors of the same organ and cell type can have remarkably diverse appearances in different patients. Furthermore, even within a single tumor, marked variations in imaging features, such as necrosis or contrast enhancement, are common. Similar spatial variations recently have been reported in genetic profiles. Radiologic heterogeneity within tumors is usually governed by variations in blood flow, whereas genetic heterogeneity is typically ascribed to random mutations. However, evolution within tumors, as in all living systems, is subject to Darwinian principles; thus, it is governed by predictable and reproducible interactions between environmental selection forces and cell phenotype (not genotype). This link between regional variations in environmental properties and cellular adaptive strategies may permit clinical imaging to be used to assess and monitor intratumoral evolution in individual patients. This approach is enabled by new methods that extract, report, and analyze quantitative, reproducible, and mineable clinical imaging data. However, most current quantitative metrics lack spatialness, expressing quantitative radiologic features as a single value for a region of interest encompassing the whole tumor. In contrast, spatially explicit image analysis recognizes that tumors are heterogeneous but not well mixed and defines regionally distinct habitats, some of which appear to harbor tumor populations that are more aggressive and less treatable than others. By identifying regional variations in key environmental selection forces and evidence of cellular adaptation, clinical imaging can enable us to define intratumoral Darwinian dynamics before and during therapy. Advances in image analysis will place clinical imaging in an increasingly central role in the development of evolution-based patient-specific cancer therapy.
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Images with different acquisition parameters can be combined to yield regions with specific combinations of quantitative image data.
“In this approach, images with different acquisition parameters (eg, contrast material–enhanced T1-weighted MR imaging, diffusion-weighted, and fluid attenuation sequences) can be combined to yield regions with specific combinations of quantitative image data.”
From Radiomics: Images Are More than Pictures, They Are Data (2016) · cites this paper as [36]
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- Authors
- Gatenby, R. A., Grove, O., & Gillies, R. J.
- Affiliations
- Moffitt Cancer Center (US)
- Venue
- Radiology
- Published
- 2013-10
- Volume
- 269
- Issue
- 1
- Pages
- 8-14
- ISSN
- 0033-8419 (ISSN-L)
- 1527-1315
- PMC
- PMC3781355
- OpenAlex
- W2124735791
- Cited by
- 515
- References
- 51
- Citations by year
- 2026: 40 · 2025: 62 · 2024: 52 · 2023: 33 · 2022: 40 · 2021: 49 · 2020: 42 · 2019: 46 · 2018: 44 · 2017: 33 · 2016: 34 · 2015: 23 · 2014: 13 · 2013: 4
- FWCI
- 3.50
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Radiology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (U54CA143970, R01CA125627, U01CA143062, R01CA170595, R01CA077575)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Radiomics and Machine Learning in Medical Imaging
- Physical Sciences › Mathematics › Modeling and Simulation › Mathematical Biology Tumor Growth
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
- Keywords
- tumor heterogeneity, tumor evolution, Darwinian selection, tumor microenvironment, tumor perfusion, tumor necrosis
- MeSH terms
- Diagnostic Imaging, Ecology, Humans, Models, Genetic, Neoplasms, Genetic Predisposition to Disease, Precision Medicine
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