Key result
Elevated serum TIMP-1 linked to ~536% greater incident cancer risk and higher cancer mortality.
Why the study?
The tumor microenvironment is regulated by matrix metalloproteinases and tissue inhibitors of metalloproteinases, but their utility as cancer biomarkers remains unclear.
Are serum TIMP-1 and MMP-8 concentrations associated with cancer incidence and mortality in a population-based cohort?
Cohort (n=8,448)
Yes
Are serum TIMP-1 and MMP-8 concentrations associated with cancer incidence and mortality in a population-based cohort?
Effect estimate: HR 6.36 (95% CI 2.50-16.16)
Elevated serum TIMP-1 levels are strongly associated with incident cancer and cancer-related mortality in older adults, suggesting its potential as a cancer biomarker.
Elevated TIMP-1 may flag higher cancer risk; hypothesis-generating in this cohort and requires prospective validation before clinical use.
The tumor microenvironment is regulated by matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs); however, their utility as cancer biomarkers remains unclear. We investigated the associations of serum MMP-8, TIMP-1, and the MMP-8/TIMP-1 ratio with prevalent and incident cancer in 8448 individuals aged 25–74 years from the FINRISK97 cohort. Participants were followed for incident cancer (n = 1618) for 26 years through the Finnish Cancer Registry. Serum MMP-8 and TIMP-1 concentrations were measured at baseline using immunoassays. Serum TIMP-1 levels were significantly higher in individuals with prevalent and incident cancer, including colorectal and lung cancer, whereas lower MMP-8 levels were observed in colorectal and prostate cancer. Accordingly, the MMP-8/TIMP-1 ratio was reduced in individuals with incident cancer. In age-stratified models adjusted for sex, smoking, and BMI, elevated TIMP-1 levels were strongly associated with incident cancer in participants aged 55–64 years (HR, 95% CI 6.36, 2.50–16.16) and ≥ 65 years (6.23, 1.67–23.21), and with cancer mortality (29.7, 8.25–106 and 18.4, 3.64–93.6). MMP-8 and the MMP-8/TIMP-1 ratio showed weaker associations with incident cancer and cancer mortality only in the 45–54-year age group. These findings support TIMP-1 as a potential biomarker for cancer risk and mortality.
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Nieminen et al. (2026) conducted a cohort in Cancer (n=8,448). Elevated serum TIMP-1 concentrations vs. Lower serum TIMP-1 concentrations was evaluated on Incident cancer in participants aged 55-64 years (HR 6.36, 95% CI 2.50-16.16). Elevated serum TIMP-1 levels were strongly associated with incident cancer (HR 6.36) and cancer mortality (HR 29.7) in participants aged 55-64 years.
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