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High plasma levels of pro-NT are associated with increased colon cancer risk

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Emerging data supports a potential role of neurotensin (NT) in the development of obesity, obesity-associated comorbidities, and certain cancers. The association of NT with colon cancer risk has not been explicitly explored. We det ermined plasma levels of pro-NT, a stable NT precursor fragment, in 223 incident colo n cancer patients and 223 age-, gender-, BMI-matched population controls participating in a population-based case-control study of colon cancer. On average, the cases have significantly higher levels of pro-NT than the controls (median = 205.6 pmol/L vs 183.1 pmol/L, respectively; P = 0.02). Multivariate logistic regression models, adjusted for age, gender, BMI, family history of colorectal cancer, smoking, diabetes mellitus, alcohol, and non-steroidal antiinflammatory drugs use, show statistically significant risk associations: for continuous measure of pro-NT, the OR estimate was 1.30 (95% CI =1.03-1.64; P = 0.026) for each increment of 175 pmol/L; for dichotomized measure of pro-NT, the OR estimate was 1.75 (95% CI = 1.12-2.74; P = 0.025) for those in the top quartile comparing to the other participants. Our results support circulating levels of pro-NT as a novel risk biomarker for colon cancer.

Original languageEnglish
Pages (from-to)641-646
Number of pages6
JournalEndocrine-Related Cancer
Volume27
Issue number11
DOIs
StatePublished - Nov 2020

Bibliographical note

Publisher Copyright:
© 2020 Society for Endocrinology.

Funding

This study was supported by the National 阀nstitutes of Health (grant numbers R01 DK112034 to B M E; U01 CA181770 and P20 CA233216 to L L). 阀n addition, we acknowledge support from the Biostatistics and Bioinformatics Shared Resource Facility of the University of Kentucky Markey Cancer Center (funded by National Cancer 阀nstitute grant number P30 CA177558 to B M E). This study was supported by the National Institutes of Health (grant numbers R01 DK112034 to B M E; U01 CA181770 and P20 CA233216 to L L). In addition, we acknowledge support from the Biostatistics and Bioinformatics Shared Resource Facility of the University of Kentucky Markey Cancer Center (funded by National Cancer Institute grant number P30 CA177558 to B M E).

FundersFunder number
The Markey Biostatistics and Bioinformatics Shared Resource Facility
National 阀nstitutes of Health
National Institutes of Health (NIH)P20 CA233216, R01 DK112034
National Childhood Cancer Registry – National Cancer InstituteP30 CA177558, U01CA181770
University of Kentucky Markey Comprehensive Cancer Center

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Biomarker
    • Intestinal hormone
    • Kentucky colon cancer genetic epidemiology study
    • Obesity
    • Pro-NT

    ASJC Scopus subject areas

    • Endocrinology, Diabetes and Metabolism
    • Oncology
    • Endocrinology
    • Cancer Research

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