Journal of Cancer Research and Therapeutics, Год журнала: 2024, Номер 20(7), С. 2141 - 2147
Опубликована: Дек. 1, 2024
Язык: Английский
Journal of Cancer Research and Therapeutics, Год журнала: 2024, Номер 20(7), С. 2141 - 2147
Опубликована: Дек. 1, 2024
Язык: Английский
Signal Transduction and Targeted Therapy, Год журнала: 2025, Номер 10(1)
Опубликована: Фев. 18, 2025
Abstract Breast cancer, characterized by unique epidemiological patterns and significant heterogeneity, remains one of the leading causes malignancy-related deaths in women. The increasingly nuanced molecular subtypes breast cancer have enhanced comprehension precision treatment this disease. mechanisms tumorigenesis progression been central to scientific research, with investigations spanning various perspectives such as tumor stemness, intra-tumoral microbiota, circadian rhythms. Technological advancements, particularly those integrated artificial intelligence, significantly improved accuracy detection diagnosis. emergence novel therapeutic concepts drugs represents a paradigm shift towards personalized medicine. Evidence suggests that optimal diagnosis models tailored individual patient risk expected are crucial, supporting era oncology for cancer. Despite rapid advancements increasing emphasis on clinical comprehensive update summary panoramic knowledge related disease needed. In review, we provide thorough overview global status including its epidemiology, factors, pathophysiology, subtyping. Additionally, elaborate latest research into contributing progression, emerging strategies, long-term management. This review offers valuable insights Cancer Research, thereby facilitating future progress both basic application.
Язык: Английский
Процитировано
27Frontiers in Immunology, Год журнала: 2025, Номер 15
Опубликована: Янв. 9, 2025
Despite enormous progress, advanced cancers are still one of the most serious medical problems in current society. Although various agents and therapeutic strategies with anticancer activity known used, they often fail to achieve satisfactory long-term patient outcomes survival. Recently, immunotherapy has shown success patients by harnessing important interactions between immune system cancer. However, many these therapies lead frequent side effects when administered systemically, prompting treatment modifications or discontinuation or, severe cases, fatalities. New approaches like intratumoral immunotherapy, characterized reduced effects, cost, systemic toxicity, offer promising prospects for future applications clinical oncology. In context locally metastatic cancer, combining diverse immunotherapeutic other targeting multiple cancer hallmarks appears crucial. Such combination hold promise improving survival promoting a sustained response. This review aims provide overview approaches, specifically focusing on administration drugs cancers. It also explores integration modalities maximize Additionally, summarizes recent advances discusses novel outlining directions field.
Язык: Английский
Процитировано
3Cell Death Discovery, Год журнала: 2024, Номер 10(1)
Опубликована: Май 18, 2024
Abstract Interactions of tumor cells with immune in the microenvironment play an important role during malignancy progression. We previously identified that GAS5 inhibited development by suppressing proliferation non-small cell lung cancer (NSCLC). Herein, we discovered a tumor-suppressing for cell-derived regulating microenvironment. positively coordinated infiltration macrophages and T NSCLC clinically, overexpression promoted recruitment both vitro vivo. Mechanistically, stabilized p53 directly binding to MYBBP1A facilitating MYBBP1A-p53 interaction, enhanced p53-mediated transcription IRF1, which activated type I interferon signaling increased production downstream CXCL10 CCL5. also found activation was associated better immunotherapy efficacy NSCLC. Furthermore, stability regulated NAT10, key enzyme responsible N4-acetylcytidine (ac4C) modification, bound mediated its ac4C modification. Collectively, could activate via MYBBP1A-p53/IRF1 axis, promoting potentially correlating efficacy, suppressed Our results suggested as promising predictive marker potential therapeutic target combination therapy
Язык: Английский
Процитировано
11Drug Resistance Updates, Год журнала: 2025, Номер 81, С. 101215 - 101215
Опубликована: Фев. 26, 2025
Язык: Английский
Процитировано
1Diagnostics, Год журнала: 2025, Номер 15(2), С. 201 - 201
Опубликована: Янв. 17, 2025
Background/Objectives: Cryotherapy is used for local tissue destruction through rapid freeze–thaw cycles. It induces cancer cell necrosis followed by inflammation in the treated tumor microenvironment, and it stimulates systemic adaptive immunity. Combining cryotherapy with immunotherapy may provide a sustained immune response preventing T exhaustion. Methods: Fifty-five patients metastatic non-small lung who had received no prior treatment were randomized into two groups 1:1 ratio: bronchoscopic group or control group. Patients up to four cycles of pembrolizumab as monotherapy combination platinum-based chemotherapy. Immune-related adverse events (irAEs), complications, size changes, overall rate (ORR), disease (DCR) evaluated. Results: Lung tumors, cryotherapy, demonstrated continuous reduction from baseline (22.4 cm2 vs. 14.4 10.2 cm2, p < 0.001). Similar changes observed pulmonary tumors (19.0 10.0 The median change between was not significant (−42.9% −27.7%, = 0.175). No differences ORR (28.6% 23.1%, 0.461) target lesion decrease (−24.0% −23.4%, 0.296) groups. However, DCR significantly higher (95.2% 73.1%, 0.049). cases serious bleeding during pneumothorax observed. Six (25.0%) eight (26.7%) experienced irAEs. Conclusions: Our study that combined without chemotherapy reduce progressive while maintaining satisfactory safety profile.
Язык: Английский
Процитировано
0Frontiers in Pharmacology, Год журнала: 2025, Номер 16
Опубликована: Март 17, 2025
Lung cancer, one of the most lethal malignancies, has seen its therapeutic strategies become a focal point significant scientific attention. Intrinsic immune signaling pathways play crucial roles in anti-tumor immunity but face clinical application challenges despite promising preclinical outcomes. Lactylation, an emerging research focus, may influences lung cancer progression by modulating functions histones and non-histone proteins. Recent findings have suggested that lactylation regulates key intrinsic molecules, including cGAS-STING, TLR, RIG-I, thereby impacting interferon expression. However, precise mechanisms which governs remain unclear. This review presents comprehensive systematic analysis relationship between emphasizes innovative perspective linking lactylation-mediated epigenetic modifications with regulation. By thoroughly examining current findings, this uncovers potential regulatory highlights implications targeting cancer. Future investigations into intricate interactions are anticipated to unveil novel targets strategies, potentially improving patient survival
Язык: Английский
Процитировано
0Experimental Hematology and Oncology, Год журнала: 2025, Номер 14(1)
Опубликована: Май 2, 2025
Abstract Hepatocellular carcinoma (HCC) is a primary liver cancer characterized by poor immune cell infiltration and strongly immunosuppressive microenvironment. Traditional treatments have often yielded unsatisfactory outcomes due to the insidious onset of disease. Encouragingly, introduction checkpoint inhibitors (ICIs) has significantly transformed approach HCC treatment. Moreover, combining ICIs with other therapies or novel materials considered most promising opportunity in HCC, some these combinations already being evaluated large-scale clinical trials. Unfortunately, trials fail meet their endpoints, few successful ones also face challenges. This indicates that potential treatment remains underutilized, prompting reevaluation this therapy. Therefore, article provides review role checkpoints treatment, research progress combination application aiming open up avenues for development safer more efficient checkpoint-related strategies Graphical abstract
Язык: Английский
Процитировано
0Journal of Controlled Release, Год журнала: 2025, Номер unknown, С. 113721 - 113721
Опубликована: Май 1, 2025
Язык: Английский
Процитировано
0Bioactive Materials, Год журнала: 2025, Номер 51, С. 634 - 649
Опубликована: Май 31, 2025
Язык: Английский
Процитировано
0Translational Oncology, Год журнала: 2024, Номер 51, С. 102175 - 102175
Опубликована: Ноя. 2, 2024
Язык: Английский
Процитировано
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