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1.
Drug Resist Updat ; 74: 101082, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38569225

RESUMO

Molecular targeted drugs and chimeric antigen receptor (CAR) T cell therapy represent specific biological treatments that have significantly improved the efficacy of treating hematologic malignancies. However, they face challenges such as drug resistance and recurrence after treatment. Combining molecular targeted drugs and CAR-T cells could regulate immunity, improve tumor microenvironment (TME), promote cell apoptosis, and enhance sensitivity to tumor cell killing. This approach might provide a dual coordinated attack on cancer cells, effectively eliminating minimal residual disease and overcoming therapy resistance. Moreover, molecular targeted drugs can directly or indirectly enhance the anti-tumor effect of CAR-T cells by inducing tumor target antigen expression, reversing CAR-T cell exhaustion, and reducing CAR-T cell associated toxic side effects. Therefore, combining molecular targeted drugs with CAR-T cells is a promising and novel tactic for treating hematologic malignancies. In this review article, we focus on analyzing the mechanism of therapy resistance and its reversal of CAR-T cell therapy resistance, as well as the synergistic mechanism, safety, and future challenges in CAR-T cell therapy in combination with molecular targeted drugs. We aim to explore the benefits of this combination therapy for patients with hematologic malignancies and provide a rationale for subsequent clinical studies.


Assuntos
Neoplasias Hematológicas , Imunoterapia Adotiva , Terapia de Alvo Molecular , Microambiente Tumoral , Humanos , Neoplasias Hematológicas/terapia , Neoplasias Hematológicas/imunologia , Neoplasias Hematológicas/tratamento farmacológico , Imunoterapia Adotiva/métodos , Imunoterapia Adotiva/tendências , Microambiente Tumoral/efeitos dos fármacos , Microambiente Tumoral/imunologia , Terapia de Alvo Molecular/métodos , Resistencia a Medicamentos Antineoplásicos/efeitos dos fármacos , Terapia Combinada/métodos , Receptores de Antígenos Quiméricos/imunologia , Antineoplásicos/uso terapêutico , Antineoplásicos/administração & dosagem , Antineoplásicos/farmacologia , Animais
2.
RSC Adv ; 13(19): 12663-12669, 2023 Apr 24.
Artigo em Inglês | MEDLINE | ID: mdl-37101527

RESUMO

As the global consumption of plastics keeps increasing, the accumulated plastics in the natural environment have threatened the survival of human beings. Photoreforming, as a simple and low-energy way, could transform wasted plastic into fuel and small organic chemicals at ambient temperature. However, the previously reported photocatalysts have some drawbacks, such as low efficiency, containing precious or toxic metal. Herein, a noble-free, non-toxic, and easy prepared mesoporous ZnIn2S4 photocatalyst has been applied in photoreforming of polylactic acid (PLA), polyethylene terephthalate (PET) and polyurethane (PU), generating small organic chemicals and H2 fuel under simulated sunlight. Plastic was degraded into small organic molecules after the pretreatment, which futher acted as the substrate for photoreforming. Mesoporous ZnIn2S4 exhibits high H2 production efficiency, strong redox ability, and long-term photostability. Furthermore, mesoporous ZnIn2S4 could overcome the hindrances of dyes and additives of realistic wasted plastic bags and bottles with high decomposition efficiency, providing an efficient and sustainable strategy for the upcycling of wasted plastics.

3.
Org Lett ; 24(22): 3944-3949, 2022 06 10.
Artigo em Inglês | MEDLINE | ID: mdl-35617159

RESUMO

Sulfonamides exhibit the advantages of wide prevalence, excellent prefunctionalization capability, and broad functional group compatibility. We report here utilizing sulfonyl imines as sulfonyl radical precursors for hydrosulfonylation of activated alkenes via visible-light irradiation. By preinstallation of functional groups into the sulfonamides and subsequent hydrosulfonylation, a variety of complex sulfones were synthesized with good efficiency under Ir/Cu dual photoredox catalysis. Additionally, this protocol expands the research in late-stage N-S bond modification in sulfonamides.


Assuntos
Alcenos , Iminas , Alcenos/química , Catálise , Iminas/química , Sulfonamidas/química , Sulfonas/química
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