TY - JOUR
T1 - Use of an optimised enzyme/prodrug combination for Clostridia directed enzyme prodrug therapy induces a significant growth delay in necrotic tumours
AU - Mowday, Alexandra M.
AU - Dubois, Ludwig J.
AU - Kubiak, Aleksandra M.
AU - Chan-Hyams, Jasmine V. E.
AU - Guise, Christopher P.
AU - Ashoorzadeh, Amir
AU - Lambin, Philippe
AU - Ackerley, David F.
AU - Smaill, Jeff B.
AU - Minton, Nigel P.
AU - Theys, Jan
AU - Patterson, Adam V.
N1 - Funding Information:
Acknowledgements This work was funded by the Health Research Council of New Zealand (Grant 14/289), the ZonMW TGO program (Grant 43400009), the Dutch Cancer Society (KWF Alpe d’HuZes Unieke Kansen #8025), the UK Biotechnology and Biological Sciences Research Council (BBSRC; grant number BB/L013940/1) and by a scholarship from the University of Auckland (awarded to AMM).
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature America, Inc. part of Springer Nature.
PY - 2022/2
Y1 - 2022/2
N2 - Necrosis is a typical histological feature of solid tumours that provides a selective environment for growth of the non-pathogenic anaerobic bacterium Clostridium sporogenes. Modest anti-tumour activity as a single agent encouraged the use of C. sporogenes as a vector to express therapeutic genes selectively in tumour tissue, a concept termed Clostridium Directed Enzyme Prodrug Therapy (CDEPT). Here, we examine the ability of a recently identified Neisseria meningitidis type I nitroreductase (NmeNTR) to metabolise the prodrug PR-104A in an in vivo model of CDEPT. Human HCT116 colon cancer cells stably over-expressing NmeNTR demonstrated significant sensitivity to PR-104A, the imaging agent EF5, and several nitro(hetero)cyclic anti-infective compounds. Chemical induction of necrosis in human H1299 xenografts by the vascular disrupting agent vadimezan promoted colonisation by NmeNTR-expressing C. sporogenes, and efficacy studies demonstrated moderate but significant anti-tumour activity of spores when compared to untreated controls. Inclusion of the pre-prodrug PR-104 into the treatment schedule provided significant additional activity, indicating proof-of-principle. Successful preclinical evaluation of a transferable gene that enables metabolism of both PET imaging agents (for vector visualisation) and prodrugs (for conditional enhancement of efficacy) is an important step towards the prospect of CDEPT entering clinical evaluation.
AB - Necrosis is a typical histological feature of solid tumours that provides a selective environment for growth of the non-pathogenic anaerobic bacterium Clostridium sporogenes. Modest anti-tumour activity as a single agent encouraged the use of C. sporogenes as a vector to express therapeutic genes selectively in tumour tissue, a concept termed Clostridium Directed Enzyme Prodrug Therapy (CDEPT). Here, we examine the ability of a recently identified Neisseria meningitidis type I nitroreductase (NmeNTR) to metabolise the prodrug PR-104A in an in vivo model of CDEPT. Human HCT116 colon cancer cells stably over-expressing NmeNTR demonstrated significant sensitivity to PR-104A, the imaging agent EF5, and several nitro(hetero)cyclic anti-infective compounds. Chemical induction of necrosis in human H1299 xenografts by the vascular disrupting agent vadimezan promoted colonisation by NmeNTR-expressing C. sporogenes, and efficacy studies demonstrated moderate but significant anti-tumour activity of spores when compared to untreated controls. Inclusion of the pre-prodrug PR-104 into the treatment schedule provided significant additional activity, indicating proof-of-principle. Successful preclinical evaluation of a transferable gene that enables metabolism of both PET imaging agents (for vector visualisation) and prodrugs (for conditional enhancement of efficacy) is an important step towards the prospect of CDEPT entering clinical evaluation.
U2 - 10.1038/s41417-021-00296-7
DO - 10.1038/s41417-021-00296-7
M3 - Article
C2 - 33558701
SN - 0929-1903
VL - 29
SP - 178
EP - 188
JO - Cancer Gene Therapy
JF - Cancer Gene Therapy
IS - 2
ER -