In1-Ghrelin Splicing Variant as a Key Element in the Pathophysiological Association Between Obesity and Prostate Cancer

Author:

Jiménez-Vacas Juan M1234ORCID,Montero-Hidalgo Antonio J1234,Gómez-Gómez Enrique135,Fuentes-Fayos Antonio C1234,Ruiz-Pino Francisco1234,Guler Ipek6,Camargo Antonio1347,Anglada Francisco J135,Carrasco-Valiente Julia135,Tena-Sempere Manuel1234,Sarmento-Cabral André1234,Castaño Justo P1234,Gahete Manuel D1234ORCID,Luque Raúl M1234ORCID

Affiliation:

1. Maimonides Institute of Biomedical Research of Cordoba (IMIBIC), Cordoba, Spain

2. Department of Cell Biology, Physiology and Immunology, University of Cordoba, Cordoba, Spain

3. Reina Sofia University Hospital (HURS), Cordoba, Spain

4. CIBER Physiopathology of Obesity and Nutrition (CIBERobn), Cordoba, Spain

5. Urology Service, HURS/IMIBIC, Cordoba, Spain

6. Leuven Biostatistics and Statistical Bioinformatics Centre (L-BioStat), Katholiek Universiteit (KU) Leuven, University of Leuven, Leuven, Belgium

7. Lipids and Atherosclerosis Unit, Internal Medicine Unit, Reina Sofia University Hospital, Cordoba, Spain

Abstract

Abstract Context Recent studies emphasize the importance of considering the metabolic status to develop personalized medicine approaches. This is especially relevant in prostate cancer (PCa), wherein the diagnostic capability of prostate-specific antigen (PSA) dramatically drops when considering patients with PSA levels ranging from 3 to 10 ng/mL, the so-called grey zone. Hence, additional noninvasive diagnostic and/or prognostic PCa biomarkers are urgently needed, especially in the metabolic-status context. Objective To assess the potential relation of urine In1-ghrelin (a ghrelin-splicing variant) levels with metabolic-related/pathological conditions (eg, obesity, diabetes, body mass index, insulin and glucose levels) and to define its potential clinical value in PCa (diagnostic/prognostic capacity) and relationship with PCa risk in patients with PSA in the grey zone. Methods Urine In1-ghrelin levels were measured by radioimmunoassay in a clinically, metabolically, pathologically well-characterized cohort of patients without (n = 397) and with (n = 213) PCa with PSA in the grey zone. Results Key obesity-related factors associated with PCa risk (BMI, diabetes, glucose and insulin levels) were strongly correlated to In1-ghrelin levels. Importantly, In1-ghrelin levels were higher in PCa patients compared to control patients with suspect of PCa but negative biopsy). Moreover, high In1-ghrelin levels were associated with increased PCa risk and linked to PCa aggressiveness (eg, tumor stage, lymphovascular invasion). In1-ghrelin levels added significant diagnostic value to a clinical model consisting of age, suspicious digital rectal exam, previous biopsy, and PSA levels. Furthermore, a multivariate model consisting of clinical and metabolic variables, including In1-ghrelin levels, showed high specificity and sensitivity to diagnose PCa (area under the receiver operating characteristic curve = 0.740). Conclusions Urine In1-ghrelin levels are associated with obesity-related factors and PCa risk and aggressiveness and could represent a novel and valuable noninvasive PCa biomarker, as well as a potential link in the pathophysiological relationship between obesity and PCa.

Funder

Ministry of Science and Innovation

Instituto de Salud Carlos III

University of Córdoba

Spanish Ministry of Universities

Marie Skłodowska-Curie

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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