Literature DB >> 17346218

CD26/dipeptidyl peptidase IV as a novel therapeutic target for cancer and immune disorders.

Michael A Thompson1, Kei Ohnuma, Masako Abe, Chikao Morimoto, Nam H Dang.   

Abstract

CD26 is a 110 kDa surface glycoprotein with intrinsic dipeptidyl peptidase IV (DPPIV) activity that is expressed on numerous cell types and has a multitude of biological functions. An important aspect of CD26 biology is its peptidase activity and its functional and physical association with molecules with key roles in various cellular pathways and biological programs. CD26 role in immune regulation has been extensively characterized, with recent findings elucidating its linkage with signaling pathways and structures involved in T-lymphocyte activation as well as antigen presenting cell-T-cell interaction. Recent work also suggests that CD26 has a significant role in tumor biology, being both a marker of disease behavior clinically as well as playing an important role in tumor pathogenesis and development. In this paper, we will review emerging data that suggest CD26 may be an appropriate therapeutic target for the treatment of selected neoplasms and immune disorders. Through the use of various experimental approaches and agents to influence CD26/DPPIV expression and activity, such as anti-CD26 antibodies, CD26/DPPIV chemical inhibitors, siRNAs to inhibit CD26 expression, overexpressing CD26 transfectants and soluble CD26 molecules, our group has shown that CD26 interacts with structures with essential cellular functions. Its association with such key molecules as topoisomerase IIalpha, p38 MAPK, and integrin beta1, has important clinical implications, including its potential ability to regulate tumor sensitivity to selected chemotherapies and to influence tumor migration/metastases and tumorigenesis. Importantly, our recent in vitro and in vivo data support the hypothesis that CD26 may indeed be an appropriate target for therapy for selected cancers and immune disorders.

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Year:  2007        PMID: 17346218     DOI: 10.2174/138955707780059853

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  18 in total

1.  DPP4 deficiency preserves cardiac function via GLP-1 signaling in rats subjected to myocardial ischemia/reperfusion.

Authors:  Hui-Chun Ku; Wen-Pin Chen; Ming-Jai Su
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2011-07-12       Impact factor: 3.000

Review 2.  Lung ischemia reperfusion injury: the therapeutic role of dipeptidyl peptidase 4 inhibition.

Authors:  Paul A J Beckers; Jan F Gielis; Paul E Van Schil; Dirk Adriaensen
Journal:  Ann Transl Med       Date:  2017-03

3.  The dietary flavonoid apigenin enhances the activities of the anti-metastatic protein CD26 on human colon carcinoma cells.

Authors:  Emilie C Lefort; Jonathan Blay
Journal:  Clin Exp Metastasis       Date:  2011-02-05       Impact factor: 5.150

4.  GLP-1 signaling preserves cardiac function in endotoxemic Fischer 344 and DPP4-deficient rats.

Authors:  Hui-Chun Ku; Wen-Pin Chen; Ming-Jai Su
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2010-09-18       Impact factor: 3.000

5.  Sitagliptin (MK0431) inhibition of dipeptidyl peptidase IV decreases nonobese diabetic mouse CD4+ T-cell migration through incretin-dependent and -independent pathways.

Authors:  Su-Jin Kim; Cuilan Nian; Christopher H S McIntosh
Journal:  Diabetes       Date:  2010-04-05       Impact factor: 9.461

Review 6.  Safety of dipeptidyl peptidase 4 inhibitors: a perspective review.

Authors:  Thomas Karagiannis; Panagiota Boura; Apostolos Tsapas
Journal:  Ther Adv Drug Saf       Date:  2014-06

7.  Dipeptidyl peptidase-4 inhibitors in type 2 diabetes may reduce the risk of autoimmune diseases: a population-based cohort study.

Authors:  Seoyoung C Kim; Sebastian Schneeweiss; Robert J Glynn; Michael Doherty; Allison B Goldfine; Daniel H Solomon
Journal:  Ann Rheum Dis       Date:  2014-06-11       Impact factor: 19.103

8.  A global comparison of the human and T. brucei degradomes gives insights about possible parasite drug targets.

Authors:  Susan T Mashiyama; Kyriacos Koupparis; Conor R Caffrey; James H McKerrow; Patricia C Babbitt
Journal:  PLoS Negl Trop Dis       Date:  2012-12-06

9.  DPP4 deficiency exerts protective effect against H2O2 induced oxidative stress in isolated cardiomyocytes.

Authors:  Hui-Chun Ku; Wen-Pin Chen; Ming-Jai Su
Journal:  PLoS One       Date:  2013-01-24       Impact factor: 3.240

10.  Downregulation of Signaling-active IGF-1 by Dipeptidyl Peptidase IV (DPP-IV).

Authors:  Ching-Ting Lin; Hsiang-Yun Tang; Yu-San Han; Hui-Ping Liu; Shiu-Feng Huang; Chia-Hui Chien; John Shyy; Jeng-Jian Chiu; Xin Chen
Journal:  Int J Biomed Sci       Date:  2010-12
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