Lipoprotein apheresis reduces circulating galectin-3 in humans
- 30 June 2015
- journal article
- research article
- Published by Wiley in Journal of Clinical Apheresis
- Vol. 31 (4), 388-392
- https://doi.org/10.1002/jca.21413
Abstract
Background: Plasma galectin-3 (Gal-3) is elevated in, and drives, diverse systemic inflammatory disorders, including cancer, cardiovascular diseases, and diabetes. Circulating Gal-3 promotes tumorigenesis and metastasis, as well as fibrotic remodeling, and is a promising therapeutic target. Apheresis has proven utility in reducing circulating disease-promoting substances, exemplified by the success of lipoprotein apheresis (LA) in abrogating cardiovascular disease progression in drug-refractory hypercholesterolemia patients. We compared the clinical utility of two FDA-approved LA systems in reducing plasma Gal-3 in humans. Methods: Plasma Gal-3 levels were assessed by ELISA in blinded samples drawn pre- and post-apheresis from hypercholesterolemia patients (n = 10/group) undergoing therapeutic LA using either a heparin-induced extracorporeal LDL precipitation (HELP) or dextran sulfate-adsorption (DSA) system. Results: Mean baseline plasma Gal-3 concentrations (±SD) were 14.3 ± 5.1 (range 6.6–22.8) and 14.5 ± 2.8 (range 10.6–19.8) ng/mL in the HELP and DSA groups, respectively. Post-apheresis Gal-3 levels were respectively reduced by 19.4% and 22.7% in the HELP (P = 0.0094) and DSA (P = 0.0027) systems (paired t-tests); the difference between devices was insignificant (P = 0.5288; Mann–Whitney). Post-treatment Gal-3 levels were 11.3 ± 3.7 (HELP; range 4.5–16.3) and 11.3 ± 3.8 (DSA; range 7.5–20.7) ng/mL. Conclusions: Circulating Gal-3 levels showed a statistically significant decrease in humans undergoing therapeutic LA. Although absolute Gal-3 reduction was ≈19–23%, this effect, combined with reducing atherogenic LDL and other inflammation mediators (e.g., CRP, fibrinogen, Lp-PLA2), may enhance apheresis clinical benefits. Applying new Gal-3-specific extraction technologies to apheresis may be advantageous in treating diverse pathologies that are promoted by elevated plasma Gal-3. J. Clin. Apheresis 31:388–392, 2016.Keywords
Funding Information
- ecoNugenics, Inc.
This publication has 25 references indexed in Scilit:
- Galectins as New Prognostic Markers and Potential Therapeutic Targets for Advanced Prostate CancersProstate Cancer, 2013
- Synergistic and Additive Effects of Modified Citrus Pectin With Two Polybotanical Compounds, in the Suppression of Invasive Behavior of Human Breast and Prostate Cancer CellsIntegrative Cancer Therapies, 2012
- Galectin-3 in Ambulatory Patients With Heart FailureCirculation: Heart Failure, 2012
- Galectin-3 – A jack-of-all-trades in cancerCancer Letters, 2011
- The regulation of inflammation by galectin‐3Immunological Reviews, 2009
- Different inflammatory responses induced by three LDL‐lowering apheresis columnsJournal of Clinical Apheresis, 2009
- Protein adsorption during LDL-apheresis: proteomic analysisNephrology Dialysis Transplantation, 2008
- Galectin-3 in apoptosis, a novel therapeutic targetJournal of Bioenergetics and Biomembranes, 2007
- H.E.L.P. Apheresis Therapy in the Treatment of Severe Hypercholesterolemia: 10 Years of Clinical ExperienceArtificial Organs, 1996
- The HELP-LDL-apheresis multicentre study, an angiographically assessed trial on the role of LDL-apheresis in the secondary prevention of coronary heart disease.European Journal of Clinical Investigation, 1991