Current status and future prospects of molecular imaging in targeting the tumor immune microenvironment DOI Creative Commons
Xiang Wang, Wen Shen, Lan Yao

и другие.

Frontiers in Immunology, Год журнала: 2025, Номер 16

Опубликована: Янв. 22, 2025

Molecular imaging technologies have significantly transformed cancer research and clinical practice, offering valuable tools for visualizing understanding the complex tumor immune microenvironment. These allow non-invasive examination of key components within microenvironment, including cells, cytokines, stromal providing crucial insights into biology treatment responses. This paper reviews latest advancements in molecular imaging, with a focus on its applications assessing interactions Additionally, challenges faced by are discussed, such as need highly sensitive specific agents, issues data integration, difficulties translation. The future outlook emphasizes potential to enhance personalized through integration artificial intelligence development novel probes. Addressing these is essential fully realizing improving diagnosis, treatment, patient outcomes.

Язык: Английский

Current and future immunotherapeutic approaches in pancreatic cancer treatment DOI Creative Commons
Pooya Farhangnia, Hossein Khorramdelazad, Hamid Nickho

и другие.

Journal of Hematology & Oncology, Год журнала: 2024, Номер 17(1)

Опубликована: Июнь 4, 2024

Abstract Pancreatic cancer is a major cause of cancer-related death, but despondently, the outlook and prognosis for this resistant type tumor have remained grim long time. Currently, it extremely challenging to prevent or detect early enough effective treatment because patients rarely exhibit symptoms there are no reliable indicators detection. Most advanced spreading that difficult treat, treatments like chemotherapy radiotherapy can only slightly prolong their life by few months. Immunotherapy has revolutionized pancreatic cancer, yet its effectiveness limited tumor's immunosuppressive hard-to-reach microenvironment. First, article explains microenvironment highlights wide range immunotherapy options, including therapies involving oncolytic viruses, modified T cells (T-cell receptor [TCR]-engineered chimeric antigen [CAR] T-cell therapy), CAR natural killer cell therapy, cytokine-induced cells, immune checkpoint inhibitors, immunomodulators, vaccines, strategies targeting myeloid in context contemporary knowledge future trends. Lastly, discusses main challenges ahead immunotherapy.

Язык: Английский

Процитировано

34

Dendritic Polymer‐Based Nanomedicines Remodel the Tumor Stroma: Improve Drug Penetration and Enhance Antitumor Immune Response DOI
Yuxin Zhang,

Zaixiang Fang,

Dayi Pan

и другие.

Advanced Materials, Год журнала: 2024, Номер 36(25)

Опубликована: Март 12, 2024

Abstract The dense extracellular matrix (ECM) in solid tumors, contributed by cancer‐associated fibroblasts (CAFs), hinders penetration of drugs and diminishes their therapeutic outcomes. A sequential treatment strategy remodeling the ECM via a CAF modifier (dasatinib, DAS) is proposed to promote an immunogenic cell death (ICD) inducer (epirubicin, Epi) apoptotic vesicles, ultimately enhancing efficacy against breast cancer. Dendritic poly(oligo(ethylene glycol) methyl ether methacrylate) (POEGMA)‐based nanomedicines (poly[OEGMA‐Dendron(G2)‐Gly‐Phe‐Leu‐Gly‐DAS] (P‐DAS) poly[OEGMA‐Dendron(G2)‐hydrazone‐Epi] (P‐Epi)) are developed for delivery DAS Epi, respectively. P‐DAS reprograms CAFs reduce collagen downregulating anabolism energy metabolism, thereby reducing deposition. regulated can enhance tumor P‐Epi strengthen its ICD effect, leading amplified antitumor immune response. In cancer‐bearing mice, this approach alleviates barrier, resulting reduced burden increased cytotoxic T lymphocyte infiltration, more encouragingly, synergizes effectively with anti‐programmed 1 (PD‐1) therapy, significantly inhibiting growth preventing lung metastasis. Furthermore, systemic toxicity barely detectable after P‐Epi. This opens new avenue treating desmoplastic tumors metabolically targeting overcome barrier.

Язык: Английский

Процитировано

21

Defining myeloid-derived suppressor cells DOI
Leila Akkari, Ido Amit, Vincenzo Bronte

и другие.

Nature reviews. Immunology, Год журнала: 2024, Номер 24(12), С. 850 - 857

Опубликована: Июль 5, 2024

Процитировано

16

Gut Microbiota-Derived Butyrate Induces Epigenetic and Metabolic Reprogramming in Myeloid-Derived Suppressor Cells to Alleviate Primary Biliary Cholangitis DOI
Rui Wang, Bo Li,

Bingyuan Huang

и другие.

Gastroenterology, Год журнала: 2024, Номер 167(4), С. 733 - 749.e3

Опубликована: Май 27, 2024

Язык: Английский

Процитировано

15

Myeloid‑derived suppressor cells: Key immunosuppressive regulators and therapeutic targets in colorectal cancer (Review) DOI Creative Commons

Wenjuan Zeng,

Haohan Liu,

Yuanhao Mao

и другие.

International Journal of Oncology, Год журнала: 2024, Номер 65(3)

Опубликована: Июль 25, 2024

Globally, colorectal cancer (CRC) is the third most common type of cancer. CRC has no apparent symptoms in early stages disease, and patients receive a confirmed diagnosis middle or late disease stages. The incidence continues to increase, affected population tends be younger. Therefore, determining how achieve an treatment become top priority for prolonging patient survival. Myeloid‑derived suppressor cells (MDSCs) are group bone marrow‑derived immuno‑negative regulatory that divided into two subpopulations, polymorphonuclear‑MDSCs monocytic‑MDSCs, based on their phenotypic similarities neutrophils monocytes, respectively. These can inhibit immune response promote cell metastasis tumour microenvironment (TME). A large aggregation MDSCs TME often marker poor prognosis inflammatory diseases intestine (such as colonic adenoma ulcerative colitis). In present review, classification first discussed. Then, amplification, role metastatic mechanism described, focusing genes, gene modifications, proteins intestinal microenvironment. Finally, progress CRC‑targeted therapies aim modulate quantity, function structure summarized hope identifying potential screening markers improving therapeutic options.

Язык: Английский

Процитировано

10

Targeted modulation of myeloid-derived suppressor cells in the tumor microenvironment: Implications for cancer therapy DOI Open Access

Yafeng Qi,

Liying Zhang,

Y Q Liu

и другие.

Biomedicine & Pharmacotherapy, Год журнала: 2024, Номер 180, С. 117590 - 117590

Опубликована: Окт. 17, 2024

Язык: Английский

Процитировано

9

Targeting lipid metabolism: novel insights and therapeutic advances in pancreatic cancer treatment DOI Creative Commons
Yanyan Zhang, Zhichao Yang, Yuchen Liu

и другие.

Lipids in Health and Disease, Год журнала: 2025, Номер 24(1)

Опубликована: Янв. 13, 2025

Lipid metabolism in cancer is characterized by dysregulated lipid regulation and utilization, critical for promoting tumor growth, survival, resistance to therapy. Pancreatic (PC) a highly aggressive malignancy of the gastrointestinal tract that has dismal 5-year survival rate less than 10%. Given essential function pancreas digestion, progression severely disrupts its function. Standard treatments PC such as surgical resection, chemotherapy, radiotherapy. However, these therapies often face significant challenges, including biochemical recurrence drug resistance. limitations, new therapeutic approaches are being developed target metabolism. Dysregulation cholesterol biosynthesis alterations fatty acids (FAs), palmitate, stearate, omega-3, omega-6, have been observed pancreatic cancer. These lipids serve energy sources, signaling molecules, components cell membranes. Their accumulation fosters an immunosuppressive microenvironment supports proliferation metastasis. Moreover, dysregulation within immune cells, particularly T impairs surveillance weakens body's defenses against Abnormal also contributes PC. Despite targeting may offer promising strategy. By enhancing peroxidation, induction ferroptosis—a form regulated death—could impair cells hinder disease progression.

Язык: Английский

Процитировано

1

Fibrinogen: a new player and target on the formation of pre-metastatic niche in tumor metastasis DOI
Yuxin Zhang, Zelin Li,

Jiamao Zhang

и другие.

Critical Reviews in Oncology/Hematology, Год журнала: 2025, Номер 207, С. 104625 - 104625

Опубликована: Янв. 17, 2025

Язык: Английский

Процитировано

1

Reinforcing cancer immunotherapy with engineered porous hollow mycobacterium tuberculosis loaded with tumor neoantigens DOI Creative Commons

Minghui Chen,

Jie Jiang, Hengyu Chen

и другие.

Journal for ImmunoTherapy of Cancer, Год журнала: 2025, Номер 13(2), С. e010150 - e010150

Опубликована: Фев. 1, 2025

Background Enhancing antigen cross-presentation is essential for the development of a tumor neoantigen vaccine. One approach to stimulate antigen-presenting cells (APCs) uptake neoantigens. Mycobacterium tuberculosis (MTb) contains pathogen-associated molecular patterns (PAMPs) recognized by APCs and adhesion molecules that facilitate MTb invasion APCs. Therefore, we suggest using as carrier enhance APC phagocytosis neoantigens, thereby promoting cross-presentation. Methods The successful preparation (phMTb) was confirmed through electron confocal microscopy. Fluorescence microscopy used detect PAMPs on phMTb well observe its role in aiding dendritic (DCs) into endosomes or lysosomes. Flow cytometry assess retention phMTb, investigate DCs, evaluate their activation maturation status, examine presentation analyze immune draining lymph nodes tissues. efficacy vaccine formulations combination with anti-programmed cell death protein 1 (PD-1) antibody therapy assessed MC38 mouse models. Adverse effects were evaluated H&E staining major organs, assessment reproductive capability detection biochemical indices. Results engineered porous hollow successfully encapsulated model without adjuvant CpG. retained surface, similar parental MTb, enhancing DC containing neoantigens Vaccines formulated facilitated maturation, activation, promoted migration phMTb-laden DCs nodes, effector memory CD8 + T lymphocyte function. In murine models, immunization phMTb-formulated vaccines elicited robust tumor-specific cytotoxic response minimal adverse effects. Additionally, vaccination effectively reversed tumor’s immune-suppressive microenvironment. Concurrent administration PD-1 exhibited significant synergistic therapeutic Conclusions results our study highlight potential clinical translation personalized carrier.

Язык: Английский

Процитировано

1

Cancer vaccines: current status and future directions DOI Creative Commons
Yi Zhou, Yuquan Wei, Xiaohe Tian

и другие.

Journal of Hematology & Oncology, Год журнала: 2025, Номер 18(1)

Опубликована: Фев. 17, 2025

Cancer continues to be a major global health burden, with high morbidity and mortality. Building on the success of immune checkpoint inhibitors adoptive cellular therapy, cancer vaccines have garnered significant interest, but their clinical remains modest. Benefiting from advancements in technology, many meticulously designed shown promise, warranting further investigations reach full potential. hold unique benefits, particularly for patients resistant other therapies, they offer ability initiate broad durable T cell responses. In this review, we highlight antigen selection vaccines, introduce responses induced by propose strategies enhance vaccine immunogenicity. Furthermore, summarize key features notable advances various platforms. Lastly, delve into mechanisms tumor resistance explore potential benefits combining standard treatments immunomodulatory approaches improve efficacy.

Язык: Английский

Процитировано

1