Control of cyclosporine A-induced tumor progression using 15-deoxyspergualin for rat cardiac transplantation.

Abstract:

:Immunosuppressive therapy increases the risk of recurrence of initial cancers in organ transplant patients, and compelling therapeutic protocols are needed to suppress the malignancy and protect the allograft. We examined the potential use of 15-deoxyspergualin (DSG) in relation to organ transplantation and cancer. The effect of DSG on established liver metastatic tumors in recipient rats bearing a heart allograft was evaluated using an in vivo luminescent technique with luciferase-expressing RCN-H4 rat colon cancer cells. The inhibition of cell growth by DSG was correlated with NF-kappa B activity and caspase-3/7 activity in vitro. In the cyclosporine A (CsA)-induced cancer progression model of rats, DSG treatment (3 mg/kg) blocked the increase in tumor-derived luciferase activity, while CsA (15 mg/kg) facilitated luciferase activity up to around day 20 after cardiac transplantation. Our data suggest that DSG may be a therapeutic candidate for the control of tumor growth in transplant patients.

journal_name

Transplantation

journal_title

Transplantation

authors

Ohsawa I,Uemoto S,Kobayashi E,Murakami T

doi

10.1097/01.tp.0000271496.75233.f6

subject

Has Abstract

pub_date

2007-08-15 00:00:00

pages

424-8

issue

3

eissn

0041-1337

issn

1534-6080

pii

00007890-200708150-00021

journal_volume

84

pub_type

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