Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?

Dipeptidyl peptidase IV (DPP-IV, CD26) is frequently dysregulated in cancer and plays an important role in regulating multiple bioactive peptides with the potential to influence cancer progression and the recruitment of immune cells. Therefore, it represents a potential contributing factor to cancer...

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Main Authors: Petr Busek, Jonathan S. Duke-Cohan, Aleksi Sedo
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/14/9/2072
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author Petr Busek
Jonathan S. Duke-Cohan
Aleksi Sedo
author_facet Petr Busek
Jonathan S. Duke-Cohan
Aleksi Sedo
author_sort Petr Busek
collection DOAJ
description Dipeptidyl peptidase IV (DPP-IV, CD26) is frequently dysregulated in cancer and plays an important role in regulating multiple bioactive peptides with the potential to influence cancer progression and the recruitment of immune cells. Therefore, it represents a potential contributing factor to cancer pathogenesis and an attractive therapeutic target. Specific DPP-IV inhibitors (gliptins) are currently used in patients with type 2 diabetes mellitus to promote insulin secretion by prolonging the activity of the incretins glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). Nevertheless, the modulation of the bioavailability and function of other DPP-IV substrates, including chemokines, raises the possibility that the use of these orally administered drugs with favorable side-effect profiles might be extended beyond the treatment of hyperglycemia. In this review, we critically examine the possible utilization of DPP-IV inhibition in cancer prevention and various aspects of cancer treatment and discuss the potential perils associated with the inhibition of DPP-IV in cancer. The current literature is summarized regarding the possible chemopreventive and cytotoxic effects of gliptins and their potential utility in modulating the anti-tumor immune response, enhancing hematopoietic stem cell transplantation, preventing acute graft-versus-host disease, and alleviating the side-effects of conventional anti-tumor treatments.
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spelling doaj.art-82783598598444559294809af6df6c1b2023-11-23T07:54:27ZengMDPI AGCancers2072-66942022-04-01149207210.3390/cancers14092072Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?Petr Busek0Jonathan S. Duke-Cohan1Aleksi Sedo2Laboratory of Cancer Cell Biology, Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University, 128 53 Prague, Czech RepublicDepartment of Medical Oncology, Dana-Farber Cancer Institute and Department of Medicine, Harvard Medical School, Boston, MA 02115, USALaboratory of Cancer Cell Biology, Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University, 128 53 Prague, Czech RepublicDipeptidyl peptidase IV (DPP-IV, CD26) is frequently dysregulated in cancer and plays an important role in regulating multiple bioactive peptides with the potential to influence cancer progression and the recruitment of immune cells. Therefore, it represents a potential contributing factor to cancer pathogenesis and an attractive therapeutic target. Specific DPP-IV inhibitors (gliptins) are currently used in patients with type 2 diabetes mellitus to promote insulin secretion by prolonging the activity of the incretins glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP). Nevertheless, the modulation of the bioavailability and function of other DPP-IV substrates, including chemokines, raises the possibility that the use of these orally administered drugs with favorable side-effect profiles might be extended beyond the treatment of hyperglycemia. In this review, we critically examine the possible utilization of DPP-IV inhibition in cancer prevention and various aspects of cancer treatment and discuss the potential perils associated with the inhibition of DPP-IV in cancer. The current literature is summarized regarding the possible chemopreventive and cytotoxic effects of gliptins and their potential utility in modulating the anti-tumor immune response, enhancing hematopoietic stem cell transplantation, preventing acute graft-versus-host disease, and alleviating the side-effects of conventional anti-tumor treatments.https://www.mdpi.com/2072-6694/14/9/2072gliptincancertumor microenvironmentimmune responsechemokinestromal cell-derived factor
spellingShingle Petr Busek
Jonathan S. Duke-Cohan
Aleksi Sedo
Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?
Cancers
gliptin
cancer
tumor microenvironment
immune response
chemokine
stromal cell-derived factor
title Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?
title_full Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?
title_fullStr Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?
title_full_unstemmed Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?
title_short Does DPP-IV Inhibition Offer New Avenues for Therapeutic Intervention in Malignant Disease?
title_sort does dpp iv inhibition offer new avenues for therapeutic intervention in malignant disease
topic gliptin
cancer
tumor microenvironment
immune response
chemokine
stromal cell-derived factor
url https://www.mdpi.com/2072-6694/14/9/2072
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