Claudin-Targeted Suicide Gene Therapy for Claudin-Overexpressing Tumor Cells by Using Modified Clostridium perfringens Enterotoxin (CPE).

Cancer Carcinoma targeting Claudin Clostridium perfringens enterotoxin Nonviral gene transfer Suicide gene therapy Tight junction proteins

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2022
Historique:
entrez: 22 6 2022
pubmed: 23 6 2022
medline: 25 6 2022
Statut: ppublish

Résumé

Bacterial toxins gain growing attention as potential cancer treatment due to their potent cytotoxic effects. Among the very different toxins with diverse modes of action, the Clostridium perfringens enterotoxin (CPE) is in focus to treat solid cancers. This toxin targets the tight junction proteins claudin-3 and -4 (Cldn-3/4), which are frequently overexpressed in solid cancers. Binding to these claudins induces pore formation in the host cell plasma membrane leading to rapid oncoleaking cell death of tumor cells. Based on this, extending the targeting of CPE beyond Cldn-3/4 is of interest, since other claudins, such as claudin-1 or -5 are often overexpressed in various cancer entities such as non-small-cell lung cancer (NSCLC) or papillary thyroid carcinoma. In this chapter we describe the modification of a CPE-encoding vector by structure-directed mutagenesis to either preferentially target Cldn-1 and -5 or to expand targeting to Cldn1-9 for improved broadened cytotoxic targeting of claudin-overexpressing tumors such as but not limited to lung cancer via CPE gene transfer.

Identifiants

pubmed: 35732998
doi: 10.1007/978-1-0716-2441-8_9
doi:

Substances chimiques

Claudins 0
Enterotoxins 0
enterotoxin, Clostridium 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

173-188

Informations de copyright

© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Walther W, Schlag PM (2013) Current status of gene therapy for cancer. Curr Opin Oncol 25:659–664. https://doi.org/10.1097/CCO.0000000000000004
doi: 10.1097/CCO.0000000000000004 pubmed: 24100345
Pahle J, Walther W (2016) Bacterial toxins for oncoleaking suicidal cancer gene therapy. In: Walther W (ed) Current strategies in cancer gene therapy, Recent results in cancer research, vol 209. Springer, Cham, pp 95–110
doi: 10.1007/978-3-319-42934-2_7
Felgner S, Kocijancic D, Frahm M, Weiss S (2016) Bacteria in cancer therapy: renaissance of an old concept. Int J Microbiol 2016:1–14
doi: 10.1155/2016/8451728
Morin PJ (2005) Claudin proteins in human cancer: promising new targets for diagnosis and therapy. Cancer Res 65(21):9603–9606
doi: 10.1158/0008-5472.CAN-05-2782
Kwon MJ (2013) Emerging roles of claudins in human cancer. Int J Mol Sci 14(9):18148–18180. https://doi.org/10.3390/ijms140918148
doi: 10.3390/ijms140918148 pubmed: 24009024 pmcid: 3794774
Michl P, Gress TM (2004) Bacteria and bacterial toxins as therapeutic agents for solid tumors. Curr Cancer Drug Targets 4(8):689–702
doi: 10.2174/1568009043332727
Soini Y, Talvensaari-Mattila A (2006) Expression of claudins 1, 4, 5, and 7 in ovarian tumors of diverse types. Int J Gynecol Pathol 25(4):330–335
doi: 10.1097/01.pgp.0000215298.38114.cc
Kominsky SL, Vali M, Korz D et al (2004) Clostridium perfringens enterotoxin elicits rapid and specific cytolysis of breast carcinoma cells mediated through tight junction proteins claudin 3 and 4. Am J Pathol 164(5):1627–1633
doi: 10.1016/S0002-9440(10)63721-2
Long H, Crean CD, Lee WH et al (2001) Expression of Clostridium perfringens enterotoxin receptors claudin-3 and claudin-4 in prostate cancer epithelium. Cancer Res 61(21):7878–7881
pubmed: 11691807
Neesse A, Hahnenkamp A, Griesmann H et al (2013) Claudin-4-targeted optical imaging detects pancreatic cancer and its precursor lesions. Gut 62(7):1034–1043. https://doi.org/10.1136/gutjnl-2012-302577
doi: 10.1136/gutjnl-2012-302577 pubmed: 22677720
Santin AD, Bellone S, Siegel ER et al (2007) Overexpression of Clostridium perfringens enterotoxin receptors claudin-3 and claudin-4 in uterine carcinosarcomas. Clin Cancer Res 13(11):3339–3346
doi: 10.1158/1078-0432.CCR-06-3037
Lu Z, Ding L, Lu Q et al (2013) Claudins in intestines: distribution and functional significance in health and diseases. Tissue Barriers 1(3):e24978. https://doi.org/10.4161/tisb.24978
doi: 10.4161/tisb.24978 pubmed: 24478939 pmcid: 3879173
Hewitt KJ, Agarwal R, Morin PJ (2006) The claudin gene family: expression in normal and neoplastic tissues. BMC Cancer 6:186. https://doi.org/10.1186/1471-2407-6-186
doi: 10.1186/1471-2407-6-186 pubmed: 16836752 pmcid: 1538620
Briggs DC, Naylor CE, Smedley JG et al (2011) Structure of the food-poisoning Clostridium perfringens enterotoxin reveals similarity to the aerolysin-like pore-forming toxins. J Mol Biol 413(1):138–149
doi: 10.1016/j.jmb.2011.07.066
Kitadokoro K, Nishimura K, Kamitani S et al (2011) Crystal structure of Clostridium perfringens enterotoxin displays features of {beta}-pore-forming toxins. J Biol Chem 286(22):19549–19555
doi: 10.1074/jbc.M111.228478
Veshnyakova A, Protze J, Rossa J et al (2010) On the interaction of Clostridium perfringens enterotoxin with claudins. Toxins 2(6):1336–1356
doi: 10.3390/toxins2061336
Harada M, Kondoh M, Ebihara C et al (2007) Role of tyrosine residues in modulation of claudin-4 by the C-terminal fragment of Clostridium perfringens enterotoxin. Biochem Pharmacol 73(2):206–214
doi: 10.1016/j.bcp.2006.10.002
McClane BA (2001) The complex interactions between Clostridium perfringens enterotoxin and epithelial tight junctions. Toxicon 39(11):1781–1791
doi: 10.1016/S0041-0101(01)00164-7
Chakrabarti G, McClane BA (2005) The importance of calcium influx, calpain and calmodulin for the activation of CaCo-2 cell death pathways by Clostridium perfringens enterotoxin. Cell Microbiol 7(1):129–146
doi: 10.1111/j.1462-5822.2004.00442.x
Eichner M, Augustin C, Fromm A et al (2017) In colon epithelia, Clostridium perfringens enterotoxin causes focal leaks by targeting claudins which are apically accessible due to tight junction derangement. J Infect Dis 217(1):147–157. https://doi.org/10.1093/infdis/jix485
doi: 10.1093/infdis/jix485 pubmed: 28968861
Piontek A, Eichner M, Zwanziger D et al (2020) Targeting claudin-overexpressing thyroid and lung cancer by modified Clostridium perfringens enterotoxin. Mol Oncol 14(2):261–276. https://doi.org/10.1002/1878-0261.12615
doi: 10.1002/1878-0261.12615 pubmed: 31825142 pmcid: 6998413
Jung JH, Jung CK, Choi HJ et al (2009) Diagnostic utility of expression of claudins in non-small cell lung cancer: different expression profiles in squamous cell carcinomas and adenocarcinomas. Pathol Res Pract 205(6):409–416. https://doi.org/10.1016/j.prp.2008.12.015
doi: 10.1016/j.prp.2008.12.015 pubmed: 19231096
Sun BS, Yao YQ, Pei BX et al (2016) Claudin-1 correlates with poor prognosis in lung adenocarcinoma. Thorac Cancer 7(5):556–563. https://doi.org/10.1111/1759-7714.12368
doi: 10.1111/1759-7714.12368 pubmed: 27766775 pmcid: 5130200
Akizuki R, Maruhashi R, Eguchi H et al (2018) Decrease in paracellular permeability and chemosensitivity to doxorubicin by claudin-1 in spheroid culture models of human lung adenocarcinoma A549 cells. Biochim Biophys Acta 1865(5):769–780
doi: 10.1016/j.bbamcr.2018.03.001
Walther W, Petkov S, Kuvardina ON et al (2012) Novel Clostridium perfringens enterotoxin suicide gene therapy for selective treatment of claudin-3 and -4 overexpressing tumors. Gene Ther 19(5):494–503
doi: 10.1038/gt.2011.136
Protze J, Eichner M, Piontek A et al (2015) Directed structural modification of Clostridium perfringens enterotoxin to enhance bind-ing to claudin-5. Cell Mol Life Sci 72(7):1417–1432
doi: 10.1007/s00018-014-1761-6
Berndt P, Winkler L, Cording J et al (2019) Tight junction proteins at the blood-brain barrier: far more than claudin-5. Cell Mol Life Sci 76(10):1987–2002. https://doi.org/10.1007/s00018-019-03030-7
doi: 10.1007/s00018-019-03030-7 pubmed: 30734065
Lacroix M (2008) Persistent use of “false” cell lines. Int J Cancer 122:1–4
doi: 10.1002/ijc.23233
Veshnyakova A, Piontek J, Protze J et al (2012) Mechanism of Clostridium perfringens enterotoxin interaction with claudin-3/-4 protein suggests structural modifications of the toxin to target specific claudin. J Biol Chem 287(3):1698–1708
doi: 10.1074/jbc.M111.312165
Shinoda T, Shinya N, Ito K et al (2016) Structural basis for disruption of claudin assembly in tight junctions by an enterotoxin. Sci Rep 6: 33632–33632

Auteurs

Laura-Sophie Beier (LS)

Division of Gastroenterology, Infectiology, Rheumatology, Clinical Physiology/Nutritional Medicine, Medical Department, Charitè - Universitätsmedizin Berlin, Berlin, Germany.
Division of Cell and Developmental Biology, Institute of Biology, University of Leipzig, Leipzig, Germany.

Jörg Piontek (J)

Division of Gastroenterology, Infectiology, Rheumatology, Clinical Physiology/Nutritional Medicine, Medical Department, Charitè - Universitätsmedizin Berlin, Berlin, Germany.

Anna Piontek (A)

Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.

Jonas Protze (J)

Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.

Dennis Kobelt (D)

Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.

Wolfgang Walther (W)

Max-Delbrück-Center for Molecular Medicine, Berlin, Germany. wowalt@mdc-berlin.de.
Experimental and Clinical Research Center, Charité Universitätsmedizin Berlin, Berlin, Germany. wowalt@mdc-berlin.de.

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