Ultrasound-Mediated Antitumor Therapy via Targeted Acoustic Release Carrier of Carbon Monoxide (TARC-CO)
Source abstract
Abstract
As one of the most valuable endogenous gas signaling molecules, carbon monoxide (CO) has been demonstrated in numerous studies to show excellent promise in the treatment of diseases, such as cancer. However, for many years, the inherent high affinity of CO for hemoglobin severely impeded the clinical transformation of CO-based treatments. Therefore, the controlled delivery of CO to target tissues has become a common challenge. Herein, an efficient ultrasonic-triggered and targeted CO release strategy was constructed based on a novel targeted acoustic release carrier of carbon monoxide (TARC-CO) that we synthesized in this study. The designed TARC-COs could afford a safe, stable, and ultrasound-guided delivery of CO in vivo by loading a specified dose of CO inside microbubbles, resulting in breast tumor suppression. Taking advantage of the high loading capacity of microbubbles, the unit volume of TARC-CO suspension could encapsulate up to 337.1 ± 8.0 (×103 ppm) of CO. In addition, the satisfactory ultrasound contrast-enhanced ability of TARC-COs achieved real-time interactive guidance and visual policing of CO delivery. For the in vitro antitumor study, TARC-COs with ultrasonic irradiation were demonstrated to effectively induce mitochondrial dysfunction by reducing mitochondrial membrane potential, leading to the apoptosis of 4T1 cells. In addition, we realized that TARC-CO-based treatment could significantly slow the growth rate of tumors by inducing apoptosis, inhibiting the proliferation of cancer cells, and limiting tumor angiogenesis. In summary, this proof-of-concept study demonstrates the feasibility and tremendous potential of TARC-COs for controlled release of CO, which can be expected to provide new inspirations and a promising perspective for therapy based on active gases.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Heme Oxygenase-1 and Carbon Monoxide · Hemoglobin structure and function · Thermal Regulation in Medicine
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China
State Key Laboratory of Membrane Biology, National Biomedical Imaging Center, Peking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing 100871, China
College of Engineering, Peking University, Beijing 100871, China
National Biomedical Imaging Center, Peking University, Beijing 100871, China
References (46)
Show source-provided references
1. 10.1590/S0100-879X199900010000110.1590/S0100-879X1999000100001 ↗
2. 10.1186/s40635-020-0292-810.1186/s40635-020-0292-8 ↗
3. 10.1002/9783527673438.ch0610.1002/9783527673438.ch06 ↗
4. 10.1073/pnas.61.2.74810.1073/pnas.61.2.748 ↗
5. 10.1002/smll.20190438210.1002/smll.201904382 ↗
6. 10.1016/j.pharmthera.2012.09.00710.1016/j.pharmthera.2012.09.007 ↗
7. 10.1002/iub.101510.1002/iub.1015 ↗
8. 10.1021/acs.inorgchem.6b0051110.1021/acs.inorgchem.6b00511 ↗
9. 10.1016/j.apsb.2020.08.00510.1016/j.apsb.2020.08.005 ↗
10. 10.1155/2017/932645410.1155/2017/9326454 ↗
11. 10.1016/j.jconrel.2015.04.02710.1016/j.jconrel.2015.04.027 ↗
12. 10.1158/0008-5472.CAN-13-107510.1158/0008-5472.CAN-13-1075 ↗
13. 10.1016/j.jinorgbio.2018.11.00310.1016/j.jinorgbio.2018.11.003 ↗
14. 10.1016/j.taap.2011.03.01310.1016/j.taap.2011.03.013 ↗
15. 10.1152/ajprenal.00363.200510.1152/ajprenal.00363.2005 ↗
16. 10.1038/nrd322810.1038/nrd3228 ↗
17. 10.1016/j.biomaterials.2020.12019310.1016/j.biomaterials.2020.120193 ↗
18. 10.1039/C5BM00210A10.1039/C5BM00210A ↗
19. 10.1161/hh0202.10453010.1161/hh0202.104530 ↗
20. 10.1021/ic902147n10.1021/ic902147n ↗
21. 10.1039/c3cc41411f10.1039/c3cc41411f ↗
22. 10.1021/jacs.5b1080010.1021/jacs.5b10800 ↗
23. 10.1002/anie.20100659810.1002/anie.201006598 ↗
24. 10.4049/jimmunol.100243310.4049/jimmunol.1002433 ↗
25. 10.1039/c0ob00099j10.1039/c0ob00099j ↗
26. 10.1021/acsomega.8b0005210.1021/acsomega.8b00052 ↗
27. 10.1021/acs.jmedchem.6b0115310.1021/acs.jmedchem.6b01153 ↗
28. 10.1021/la102943210.1021/la1029432 ↗
29. 10.7150/ntno.4380810.7150/ntno.43808 ↗
30. 10.1016/j.canlet.2015.02.05210.1016/j.canlet.2015.02.052 ↗
31. 10.1016/j.healun.2020.02.00210.1016/j.healun.2020.02.002 ↗
32. 10.1021/acsami.7b0534610.1021/acsami.7b05346 ↗
33. 10.1021/acsami.1c0601410.1021/acsami.1c06014 ↗
34. 10.1039/C8NR08451C10.1039/C8NR08451C ↗
35. 10.1126/scitranslmed.300367910.1126/scitranslmed.3003679 ↗
36. Romão C. C. · 2015 · 165
37. 10.1016/S1076-6332(03)80203-910.1016/S1076-6332(03)80203-9 ↗
38. 10.7150/thno.441010.7150/thno.4410 ↗
39. 10.2174/138920101466613122611461110.2174/1389201014666131226114611 ↗
40. 10.14366/usg.1702110.14366/usg.17021 ↗
41. 10.1016/j.ultrasmedbio.2006.07.01610.1016/j.ultrasmedbio.2006.07.016 ↗
42. 10.1016/j.pbiomolbio.2006.07.02710.1016/j.pbiomolbio.2006.07.027 ↗
43. 10.1016/j.biomaterials.2019.04.00410.1016/j.biomaterials.2019.04.004 ↗
44. 10.3748/wjg.v21.i22.692410.3748/wjg.v21.i22.6924 ↗
45. 10.1196/annals.1413.00110.1196/annals.1413.001 ↗
46. 10.1111/j.1365-2559.2006.02402.x10.1111/j.1365-2559.2006.02402.x ↗