Blood tests could identify early signs of cancer years before diagnosis
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A study of blood samples collected up to nine years before a cancer diagnosis found changes in the DNA that captured the body's response to early traces of cancer development.
The findings, published in Cell Genomics, build on other recent work by researchers at Oxford Population Health and the University of Toronto aimed at identifying the earliest signs of cancer development through highly sensitive blood profiling that captures DNA changes.
Cancer remains the second leading cause of death globally, with deaths often resulting from a late diagnosis. When cancers are detected early, treatment is more likely to succeed, and patients have a better chance of surviving.
Routine screening tests remain limited to a few cancers, such as Pap smears for cervical cancer and stool tests for bowel cancer. For other cancers, early detection through radiological imaging to look for tumors or examination of a tissue sample to look for cellular abnormalities varies in effectiveness. Recent developments in liquid biopsies offer the possibility of detecting cancer in its earliest stages using minimally invasive blood or urine tests.
DNA reveals markers for people at high risk
Currently, liquid biopsies are mainly used after a cancer diagnosis to find and analyze DNA from existing tumors or to track potential recurrence. For this study, the researchers examined blood samples collected from people who were months or years away from a cancer diagnosis to determine whether their DNA would reveal the earliest biological changes associated with cancer development.
They used stored blood samples from 491 participants in the Ontario Health Study who were cancer-free when their blood was collected. Some subsequently developed breast or prostate cancer, while others remained cancer-free. The researchers looked for differences in chemical patterns in the DNA known as methylation. These tiny chemical tags act like switches that control gene activity linked to functions such as cell growth, immune function and inflammation.
They found that prostate cancer produced the strongest early signal through methylation changes in DNA regions called silencers, which normally help switch genes off. Using these markers, the researchers could identify people at high risk of developing prostate cancer 5 to 8 years before a diagnosis. With no current population-wide screening program for prostate cancer, the authors suggest that this type of testing could eventually help identify people who need more proactive screening while reducing unnecessary testing in low-risk individuals.
Breast cancer was more difficult to detect but still showed some early signals through methylation changes in DNA regions called enhancers. Although the test's overall accuracy was lower than for prostate cancer, it could still distinguish women at higher and lower risk of developing breast cancer 1.5 to 8 years before a diagnosis. The authors note that for breast cancer, the test is unlikely to be accurate enough for population-wide screening but could be useful as a complementary risk-assessment tool.
Blood tests could support future cancer screening
Philip Awadalla, professor of molecular genetics at Oxford Population Health and the University of Oxford's Big Data Institute, said the study represents an important next step in a broader research program using cell-free methylated DNA immunoprecipitation sequencing.
Earlier studies established that this approach could detect and classify multiple tumor types, distinguish localized from metastatic prostate cancer, and identify advanced breast cancer and its estrogen-receptor status. Most recently, the team contributed to a resource drawing on nearly 1,300 blood samples from multiple cancer types showing that patterns in DNA methylation can improve detection of a wide range of cancers.
Awadalla said, "Together, these studies chart a progression from detecting established tumors to identifying the earliest systemic signals of cancer development—supporting a future in which minimally invasive blood tests could complement existing screening and help identify people who would benefit most from closer surveillance."
Publication details
Nicholas Cheng et al, Pre-diagnosis plasma cell-free DNA reveals early signatures of prostate and breast cancer risk up to eight years prior to clinical detection, Cell Genomics (2026). DOI: 10.1016/j.xgen.2026.101364
Journal information: Cell Genomics
Key medical concepts
DNA MethylationProstate CancerBreast Cancer
Clinical categories
OncologyCommon illnesses & PreventionLaboratory medicine Provided by University of Oxford Who's behind this story?
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