AI Article Synopsis

  • The study investigates the role of proprotein convertase subtilisin/kexin type 9 (PCSK9) in cholesterol regulation as a potential biomarker for breast cancer risk in premenopausal women.
  • A cohort of 235 women was followed for 17 years within a clinical trial comparing tamoxifen, fenretinide, and placebo, while measuring plasma levels of PCSK9 and their associations with breast cancer events.
  • Results showed no significant correlation between high PCSK9 levels and breast cancer risk, but identified a negative correlation between PCSK9 and estradiol levels, alongside various cholesterol metrics.

Article Abstract

Background And Aim: The involvement of cholesterol in cancer development remains a topic of debate, and its association with breast cancer has yet to be consistently demonstrated. Considering that circulating cholesterol levels depend on several concomitant processes, we tested the liability of plasma levels of proprotein convertase subtilisin/kexin type 9 (), one of the key regulators of cholesterol levels, as a prognostic biomarker in the context of breast neoplastic events.

Methods: Within a prospective randomized breast cancer prevention trial we measured baseline plasma levels of . A total of 235 at-risk premenopausal women were randomized and followed up for 17 years. Participants enrolled in this placebo-controlled, phase II, double-blind trial were randomly assigned to receive either tamoxifen 5 mg/d or fenretinide 200 mg/d, both agents, or placebo for 2 years. The associations with breast cancer events were evaluated through competing risk and Cox regression survival models, adjusted for randomization strata (5-year Gail risk ≥ 1.3% vs. intraepithelial neoplasia or small invasive breast cancer of favorable prognosis), age, and treatment allocation. associations with biomarkers linked to breast cancer risk were assessed on blood samples collected at baseline.

Results: The plasmatic median and interquartile range were 207 ng/mL and 170-252 ng/mL, respectively. Over a median follow-up period of 17 years and 89 breast neoplastic events, disease-free survival curves showed a hazard ratio of 1.002 (95% CI: 0.999-1.005, = 0.22) for women with plasma levels ≥ 207 ng/mL compared to women with levels below 207 ng/mL. No differences between randomization strata were observed. We found a negative correlation between and estradiol (r = -0.305), maintained even after partial adjustment for BMI and age (r = -0.287). Cholesterol (r = 0.266), LDL-C (r = 0.207), non-HDL-C (r = 0.246), remnant cholesterol (r = 0.233), and triglycerides (r = 0.233) also correlated with .

Conclusions: In premenopausal women at risk of early-stage breast cancer, did not appear to have a role as a prognostic biomarker of breast neoplastic events. Larger studies are warranted investigating patients in different settings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11011028PMC
http://dx.doi.org/10.3390/cancers16071411DOI Listing

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