Bacterial Expression of Promelittin for Safe and Effective Tumor Therapy
Source abstract
Abstract
Bacteria-based tumor therapy has attracted much attention due to its unique mechanism and abundant application. With the rapid development of synthetic biology, utilizing gene technology to make bacteria express therapeutic agents has greatly innovated bacterial therapy paradigms. Herein, we constructed an Escherichia coli expressing promelittin protein system based on the Trojan horse strategy, which limited the toxicity of melittin through the fusion protein during melittin expression. After targeted colonization of bacteria in tumor tissues, promelittin was activated by matrix metalloproteinase, followed by causing tumor cell death through a membrane-lytic mechanism. Additionally, the released cytolytic melittin in turn killed the maternal bacteria, eliminating safety hazards and triggering host immunity. Detailed experiments revealed that the bacteria expressing the promelittin system could significantly inhibit the proliferation and metastasis of primitive tumors in a CT26-bearing mice model. This study sheds insights into the development of bacteria-based synergistic tumor therapy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Cancer Research and Treatments · Virus-based gene therapy research · Nanoplatforms for cancer theranostics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan 430062, P. R. China
Funding
National Key Research and Development Program of China · Department of Science and Technology of Hubei Province · National Natural Science Foundation of China
References (38)
Show source-provided references
1. 10.1021/acsnano.2c0350910.1021/acsnano.2c03509 ↗
2. 10.1021/acsami.2c1108910.1021/acsami.2c11089 ↗
3. 10.1002/smll.20220577210.1002/smll.202205772 ↗
4. 10.1002/adma.20210393610.1002/adma.202103936 ↗
5. 10.1016/j.nantod.2020.10096010.1016/j.nantod.2020.100960 ↗
6. 10.1016/j.addr.2015.12.00210.1016/j.addr.2015.12.002 ↗
7. 10.1038/s41467-021-26367-910.1038/s41467-021-26367-9 ↗
8. 10.1038/s41587-022-01456-210.1038/s41587-022-01456-2 ↗
9. 10.1002/adma.20210651610.1002/adma.202106516 ↗
10. 10.1073/pnas.202060611810.1073/pnas.2020606118 ↗
11. 10.1097/00000658-189112000-0001510.1097/00000658-189112000-00015 ↗
12. 10.1126/science.aay918910.1126/science.aay9189 ↗
13. 10.1021/acsami.2c0149310.1021/acsami.2c01493 ↗
14. 10.1002/advs.20210508610.1002/advs.202105086 ↗
15. 10.1126/sciadv.aba354610.1126/sciadv.aba3546 ↗
16. 10.1126/science.add966710.1126/science.add9667 ↗
17. 10.1038/s41586-023-05870-710.1038/s41586-023-05870-7 ↗
18. 10.1002/advs.20200357210.1002/advs.202003572 ↗
19. 10.1038/s41551-017-0181-y10.1038/s41551-017-0181-y ↗
20. 10.1038/s41568-018-0070-z10.1038/s41568-018-0070-z ↗
21. 10.1038/s41586-021-04003-210.1038/s41586-021-04003-2 ↗
22. 10.1126/scitranslmed.aak953710.1126/scitranslmed.aak9537 ↗
23. 10.1038/s41467-020-16602-010.1038/s41467-020-16602-0 ↗
24. 10.1002/adfm.20200974410.1002/adfm.202009744 ↗
25. 10.1038/s41551-022-00886-210.1038/s41551-022-00886-2 ↗
26. 10.1038/s41591-019-0498-z10.1038/s41591-019-0498-z ↗
27. 10.1039/D0CS01571G10.1039/D0CS01571G ↗
28. 10.1021/acsami.1c1761810.1021/acsami.1c17618 ↗
29. 10.1038/cr.2017.13310.1038/cr.2017.133 ↗
30. 10.1186/s12967-016-0910-010.1186/s12967-016-0910-0 ↗
31. 10.1002/advs.20190186610.1002/advs.201901866 ↗
32. 10.1073/pnas.040819110110.1073/pnas.0408191101 ↗
33. 10.1038/s41586-021-03368-810.1038/s41586-021-03368-8 ↗
34. 10.1158/0008-5472.CAN-04-300210.1158/0008-5472.CAN-04-3002 ↗
35. 10.1002/smll.20210293210.1002/smll.202102932 ↗
36. 10.1126/science.aan423610.1126/science.aan4236 ↗
37. 10.1126/science.abp956310.1126/science.abp9563 ↗
38. 10.1002/adma.20200208510.1002/adma.202002085 ↗