Biomedicine & Pharmacotherapy, Год журнала: 2025, Номер 185, С. 117986 - 117986
Опубликована: Март 15, 2025
Язык: Английский
Biomedicine & Pharmacotherapy, Год журнала: 2025, Номер 185, С. 117986 - 117986
Опубликована: Март 15, 2025
Язык: Английский
Toxicology Reports, Год журнала: 2025, Номер 14, С. 101902 - 101902
Опубликована: Янв. 10, 2025
Язык: Английский
Процитировано
0Elsevier eBooks, Год журнала: 2025, Номер unknown, С. 325 - 340
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0Frontiers in Oncology, Год журнала: 2025, Номер 14
Опубликована: Янв. 21, 2025
Gastric cancer remains a leading cause of cancer-related mortality worldwide, with advanced stages presenting significant challenges due to metastasis and drug resistance. Traditional Chinese Medicine (TCM) offers promising complementary approach characterized by holistic treatment principles minimal side effects. This review comprehensively explores the multifaceted mechanisms which TCM addresses gastric cancer. Specifically, we detail how inhibits aerobic glycolysis downregulating key glycolytic enzymes metabolic pathways, thereby reducing energy supply essential for cell proliferation. We examine suppresses angiogenesis targeting vascular endothelial growth factor (VEGF) cyclooxygenase-2 (COX-2) effectively starving tumors nutrients oxygen required metastasis. Furthermore, modulates immune microenvironment enhancing activity effector cells such as CD4 + CD8 T natural killer (NK) while immunosuppressive like regulatory (Tregs) myeloid-derived suppressor (MDSCs). These actions collectively contribute slowing tumor progression, inhibiting metastasis, body’s antitumor response. The insights presented underscore potential an integral component comprehensive strategies, highlighting avenues future research clinical application improve patient outcomes.
Язык: Английский
Процитировано
0Cancer Letters, Год журнала: 2025, Номер unknown, С. 217527 - 217527
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0Journal of Translational Medicine, Год журнала: 2025, Номер 23(1)
Опубликована: Фев. 10, 2025
Resistance to treatment is a critical factor contributing poor prognosis in gastric cancer patients. HSP90 has emerged as promising therapeutic target; however, its role regulating tumor metabolic pathways, particularly glycolysis, remains poorly understood, which limits clinical application. We identified proteins that directly interact with using immunoprecipitation (IP) followed by mass spectrometry. The relationship between and glycolysis was further investigated through transcriptomic analyses vitro experiments. Mechanistic insights were obtained spectrometry, co-immunoprecipitation (Co-IP) assays, drug sensitivity tests, bioinformatics analyses. Additionally, we developed scoring system based on data evaluate prognostic significance association resistance Our multi-omics studies revealed regulates influences the stemness properties of cells. Mechanistically, facilitates assembly glycolytic multi-enzyme complex, termed HGEO enhances metabolism. formation multienzyme complex comprising key enzymes including PGK1, PKM2, ENO1, LDHA, thereby facilitating production final products. refer this "HSP90-Glycolytic Output Complex" (HGEO Complex). quantified phenomenon (HGScore), finding patients high HGScore exhibited more malignant signatures, increased treatment, poorer prognoses. Furthermore, demonstrated localized nucleus, regulated nuclear lamina protein LMNA, contributes adverse outcomes. In experiments indicated inhibiting sensitizes cells chemotherapy. findings suggest LMNA mediated localization enhancing traits mechanisms cancer. Targeting pathway may offer novel strategy improve
Язык: Английский
Процитировано
0Journal of Ethnopharmacology, Год журнала: 2025, Номер unknown, С. 119479 - 119479
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Stem Cell Research & Therapy, Год журнала: 2025, Номер 16(1)
Опубликована: Фев. 23, 2025
Язык: Английский
Процитировано
0Journal of Ethnopharmacology, Год журнала: 2025, Номер 345, С. 119584 - 119584
Опубликована: Март 3, 2025
Язык: Английский
Процитировано
0Cell Death Discovery, Год журнала: 2025, Номер 11(1)
Опубликована: Март 3, 2025
Abstract Transcriptional dysregulation is a hallmark of cancer initiation and progression, driven by genetic epigenetic alterations. Enhancer reprogramming has emerged as pivotal driver carcinogenesis, with cells often relying on aberrant transcriptional programs. The advent high-throughput sequencing technologies provided critical insights into enhancer events their role in malignancy. While targeting enhancers presents promising therapeutic strategy, significant challenges remain. These include the off-target effects enhancer-targeting technologies, complexity redundancy networks, dynamic nature reprogramming, which may contribute to resistance. This review comprehensively encapsulates structural attributes enhancers, delineates mechanisms underlying malignant transformation, evaluates opportunities limitations associated cancer.
Язык: Английский
Процитировано
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