2019
DOI: 10.1126/scitranslmed.aat5690
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Autologous tumor cell–derived microparticle-based targeted chemotherapy in lung cancer patients with malignant pleural effusion

Abstract: This study investigated the application of a therapeutic tumor cell–derived microparticle-based nanodelivery platform in malignant pleural effusion.

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Cited by 149 publications
(84 citation statements)
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References 60 publications
(62 reference statements)
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“…Conversely, modified or engineered EVs can be used as vaccines to provide anti-tumor immunity [88]. Previous experiments have shown that UV-exposed lung cancer TDEs are capable of promoting DC maturation and inducing T cell-dependent anti-tumor immunity, compared to normally secreted TDEs [89,90]. The DNA in TDEs was found to engage the cGAS/STING pathway and possibly be involved in the process underlying DC maturation.…”
Section: Cancer Vaccinementioning
confidence: 99%
“…Conversely, modified or engineered EVs can be used as vaccines to provide anti-tumor immunity [88]. Previous experiments have shown that UV-exposed lung cancer TDEs are capable of promoting DC maturation and inducing T cell-dependent anti-tumor immunity, compared to normally secreted TDEs [89,90]. The DNA in TDEs was found to engage the cGAS/STING pathway and possibly be involved in the process underlying DC maturation.…”
Section: Cancer Vaccinementioning
confidence: 99%
“…For CEVs loaded with chemotherapeutic agents, the process of irradiation was able to improve the efficacy in the cancer treatment (51). Another study showed that compared with the PBS group, CEVs of A549 lung cancer promoted the progression of cancer and malignant pleural effusion, while the irradiated CEVs group showed no significant change in the cancer progression (25). Additionally, the irradiated and drug-loaded CEVs of A549 lung cancer inhibited the progression of cancer and malignant pleural effusion in the clinical tests (25,52).…”
Section: Irradiated Cancer Cells-derived Extracellular Vesiclesmentioning
confidence: 99%
“…The injections of cisplatin-loaded CEVs were administered intrathoracically four times, and the results exhibited a 95% reduction in tumor cells in the MPE. In another clinical study with methotrexate-loaded CEVs (25), autologous tumor cells were prepared from patients' MPE and incubated with chemotherapeutic methotrexate after ultraviolet irradiation. The methotrexate-loaded CEVs were collected by ultracentrifugation.…”
Section: Chemotherapeutic Drugs Loaded Cancer Cells-derived Vesiclesmentioning
confidence: 99%
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