Target tumor therapy in human gastric cancer cells through the combination of docetaxel-loaded cationic lipid microbubbles and ultrasound-triggered microbubble destruction
It is well accepted that ultrasound-induced microbubble (USMB) cavitation is a promising method for drug delivery. Ultrasound-targeted destruction of cytotoxic drug-loaded lipid microbubbles (LMs) is used to promote the treatment of cancer. This study aimed to investigate the antitumor effects from...
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Veröffentlicht in: | Functional & integrative genomics 2023-03, Vol.23 (1), p.59-59, Article 59 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | It is well accepted that ultrasound-induced microbubble (USMB) cavitation is a promising method for drug delivery. Ultrasound-targeted destruction of cytotoxic drug-loaded lipid microbubbles (LMs) is used to promote the treatment of cancer. This study aimed to investigate the antitumor effects from a combination of docetaxel-loaded cationic lipid microbubbles (DLLM
+
) and ultrasound (US)-triggered microbubble destruction (UTMD) on gastric cancer (GC). It was found that the functional dose of DOC in this study was 1 × 10
−9
mol/L. We found that DLLM combined with the UTMD group showed greater growth inhibition of the cultured human gastric cancer cells (HGCCs) when compared with the other five groups by arresting the G
2
/M phase in the cell cycle. However, DLLM
+
combined with UTMD showed a higher inhibition rate of tumor growth than DLLM combined with UTMD and that of the RC/CMV-p16 combined with UTMD in vitro and in vivo experiments. DLLM
+
combined with UTMD significantly suppressed proliferation and promoted the apoptosis of HGCCs with more cells arrested in the G
2
/M phase. In addition, DLLM
+
combined with UTMD suppressed the proliferation and induced apoptosis by arresting cells in the G
2
/M phase, which led to a great inhibition of GC progression. Thus, our results indicated that the combination of DLLM
+
and UTMD might represent a novel and promising approach to chemotherapy for GC. |
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ISSN: | 1438-793X 1438-7948 |
DOI: | 10.1007/s10142-022-00952-7 |