International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113447 - 113447
Опубликована: Ноя. 7, 2024
Язык: Английский
International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113447 - 113447
Опубликована: Ноя. 7, 2024
Язык: Английский
Biomaterials, Год журнала: 2024, Номер 313, С. 122766 - 122766
Опубликована: Авг. 22, 2024
Язык: Английский
Процитировано
8Research Square (Research Square), Год журнала: 2025, Номер unknown
Опубликована: Янв. 20, 2025
Язык: Английский
Процитировано
0Journal of drug targeting, Год журнала: 2025, Номер unknown, С. 1 - 43
Опубликована: Фев. 19, 2025
In the dynamic arena of cancer therapeutics, chemoimmunotherapy has shown tremendous promise, especially for aggressive forms breast like triple-negative (TNBC). This review delves into significant role liposomes in enhancing effectiveness by leveraging cancer-specific mechanisms such as induction immunogenic cell death (ICD), reprogramming tumor microenvironment (TME), and enabling sequential drug release. We examine innovative dual-targeting that capitalize on heterogeneity, well pH-sensitive formulations offer improved control over delivery. Unlike prior analyses, this directly links advancements preclinical research-such PAMAM dendrimer-based nanoplatforms RGD-decorated liposomes-to clinical trial results, highlighting their potential to revolutionize TNBC treatment strategies. Additionally, we address ongoing challenges related scalability, toxicity, regulatory compliance, propose future directions personalized, immune-focused nanomedicine. work not only synthesizes latest research but also offers a framework translating liposomal from laboratory practice.
Язык: Английский
Процитировано
0Frontiers in Immunology, Год журнала: 2025, Номер 16
Опубликована: Март 19, 2025
Complete surgical resection of advanced breast cancer is highly challenging and often leaves behind microscopic tumor foci, leading to inevitable relapse. Postoperative formation the immunosuppressive microenvironment (TME) reduces efficacy immunotherapies against residual tumors. Although cytotoxic chemotherapeutics exert capacity intensify immunotherapy via immunogenic cell death (ICD) effects, systemically administered chemo agents cannot access sites, fail elicit antitumor immune responses. Herein, we present a novel syringeable immunotherapeutic hydrogel (SiGel@SN38/aOX40) loaded with DNA-targeting chemotherapeutic 7-ethyl-10-hydroxycamptothecin (SN38) anti-OX40 agonist antibody (aOX40). The sustained in-site release SN38 aOX40 activate stimulator interferon genes (STING) pathway, type I interferons expression, synergistically facilitate dendritic (DC) activation, initiate persistent T mediated responses within bed that eliminate tumors no recurrence in 120 days. Collectively, our designed SiGel@SN38/aOX40 induces robust long-lasting tumoricidal immunity following exhibit immense potential for clinical translation.
Язык: Английский
Процитировано
0Acta Biomaterialia, Год журнала: 2025, Номер unknown
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0European Polymer Journal, Год журнала: 2024, Номер 219, С. 113379 - 113379
Опубликована: Авг. 9, 2024
Язык: Английский
Процитировано
3PeerJ, Год журнала: 2024, Номер 12, С. e18559 - e18559
Опубликована: Ноя. 22, 2024
Lung cancer (LC) remains one of the most prevalent and lethal malignancies globally, with a 5-year survival rate for advanced cases persistently below 10%. Despite significant advancements in immunotherapy, substantial proportion patients LC fail to respond effectively these treatments, highlighting an urgent need novel immunotherapeutic targets. The cyclic GMP-AMP synthase (cGAS)-stimulator interferon genes (STING) pathway has gained prominence as potential target improving immunotherapy due its pivotal role enhancing anti-tumor immune responses, augmenting tumor antigen presentation, promoting T cell infiltration. However, emerging evidence also suggests that cGAS-STING may have pro-tumorigenic effects context LC. This review aims provide comprehensive analysis pathway, including biological composition, activation mechanisms, physiological functions, well dual roles current treatment strategies pathway. By addressing aspects, we intend highlight target, while considering challenges future directions clinical application.
Язык: Английский
Процитировано
2EBioMedicine, Год журнала: 2024, Номер 111, С. 105491 - 105491
Опубликована: Дек. 6, 2024
Язык: Английский
Процитировано
2International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(16), С. 8836 - 8836
Опубликована: Авг. 14, 2024
Colorectal cancer (CRC) affects approximately 2 million people worldwide. Obesity is the major risk factor for CRC. In addition, obesity contributes to a chronic inflammatory stage that enhances tumor progression through secretion of proinflammatory cytokines. addition an increased response, obesity-associated presents accrued molecular factors related characteristics, such as genome instability, sustained cell proliferation, telomere dysfunctions, angiogenesis, and microbial alteration, among others. Despite evidence accumulated over last few years, treatments CRC do not differ from in normal-weight individuals. this review, we summarize current knowledge on cancer, including its epidemiology, factors, treatments. Finally, enumerate possible new therapeutic targets may improve conditions obese patients. key development CRC, resulting reversal should be considered strategy improving antineoplastic therapies.
Язык: Английский
Процитировано
2International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113447 - 113447
Опубликована: Ноя. 7, 2024
Язык: Английский
Процитировано
2