Biochimica et Biophysica Acta (BBA) - General Subjects, Год журнала: 2024, Номер 1868(6), С. 130599 - 130599
Опубликована: Март 22, 2024
Язык: Английский
Biochimica et Biophysica Acta (BBA) - General Subjects, Год журнала: 2024, Номер 1868(6), С. 130599 - 130599
Опубликована: Март 22, 2024
Язык: Английский
Nutrients, Год журнала: 2024, Номер 16(11), С. 1642 - 1642
Опубликована: Май 27, 2024
Liver cancer ranks third globally among causes of cancer-related deaths, posing a significant public health challenge. However, current treatments are inadequate, prompting growing demand for novel, safe, and effective therapies. Natural products (NPs) have emerged as promising candidates in drug development due to their diverse biological activities, low toxicity, minimal side effects. This paper begins by reviewing existing treatment methods drugs liver cancer. It then summarizes the therapeutic effects NPs sourced from various origins on Finally, we analyze potential mechanisms treating cancer, including inhibition angiogenesis, migration, invasion; regulation cell cycle; induction apoptosis, autophagy, pyroptosis, ferroptosis; influence tumor metabolism; immune regulation; intestinal function; key signaling pathways. systematic review aims provide comprehensive overview research treatment, offering foundation further application pharmaceuticals functional foods.
Язык: Английский
Процитировано
10International Journal of Nanomedicine, Год журнала: 2024, Номер Volume 19, С. 3461 - 3473
Опубликована: Апрель 1, 2024
Purpose: Ivosidenib (IVO), an isocitrate dehydrogenase-1 (IDH1) used for treatment of acute myeloid leukemia (AML) and cholangiocarcinoma.However, poor solubility, low bioavailability, high dose side effects limit clinical application IVO.Methods: Ivosidenib-loaded PLGA nanoparticles (IVO-PLGA-NPs) chitosan coated (IVO-CS-PLGA-NPs) were prepared using emulsification solvent evaporation method the liver cancer. Results:The developed IVO-PLGA-NPs evaluated their particle size (171.7±4.9 nm), PDI (0.333), ZP (-23.0±5.8 mV), EE (96.3±4.3%), DL (9.66±1.1%);similarly, IVO-CS-PLGA-NPs (177.3±5.2 (0.311), +25.9±5.7 mV, (90.8±5.7%), (9.42±0.7%).The coating was evidenced by increase in mean positive value.Because coating, showed a more stable prolonged release IVO than IVO-PLGA-NPs.In comparison to pure-IVO, found be effective against HepG2 cells, with IC 50 values MTT assay being approximately half those pure-IVO.In expressions caspase-3, caspase-9, p53 significantly (p < 0.05) elevated.Conclusion: Overall, these findings suggest that improves delivery efficacy ivosidenib cancer treatment.
Язык: Английский
Процитировано
9Journal of Asian Natural Products Research, Год журнала: 2025, Номер unknown, С. 1 - 13
Опубликована: Фев. 22, 2025
Esculetin is a coumarin compound with anticancer, antioxidant, and anti-inflammatory activities. In this study, we synthesized an esculetin derivative, 6,7-bis(Pentyloxy)-2H-Chromen-2-One (BPCO), through etherification. BPCO inhibited the proliferation of HepG2 cells in dose- time-dependent manner. It also cell migration, promoted apoptosis, caused cycle arrest at G1 phase. Additionally, downregulated expression levels Bcl-2 Bcl-XL upregulated Bax Bak. This study shows that inhibits hepatocellular carcinoma induces providing basis for further as antitumor agent.
Язык: Английский
Процитировано
1International Journal of Molecular Sciences, Год журнала: 2023, Номер 24(12), С. 10354 - 10354
Опубликована: Июнь 19, 2023
There is no doubt that significant progress has been made in tumor therapy the past decades. However, discovery of new molecules with potential antitumor properties still remains one most challenges field anticancer therapy. Nature, especially plants, a rich source phytochemicals pleiotropic biological activities. Among plethora phytochemicals, chalcones, bioprecursors flavonoid and isoflavonoids synthesis higher have attracted attention due to broad spectrum activities clinical applications. Regarding antiproliferative effects multiple mechanisms action including cell cycle arrest, induction different forms death modulation various signaling pathways documented. This review summarizes current knowledge related natural chalcones types malignancies breast cancers, cancers gastrointestinal tract, lung renal bladder melanoma.
Язык: Английский
Процитировано
21Frontiers in Pharmacology, Год журнала: 2023, Номер 14
Опубликована: Март 21, 2023
Primary liver cancer is the second leading cause of tumor-related deaths in China, with hepatocellular carcinoma (HCC) accounting for 80%–90% these. Since there a lack symptoms early stages HCC, large proportion patients were identified unresectable HCC when diagnosed. Due to severe resistance chemotherapy, advanced traditionally treated systematic therapy past decades, and tyrosine kinase inhibitor (TKI) sorafenib has remained only treatment option since 2008. Immunotherapies, particularly immune checkpoint inhibitors (ICIs), have shown strong anti-tumor effect been supported by several guidelines recently. ICIs, example programmed cell death-1 (PD-1) such as nivolumab pembrolizumab, death ligand 1 (PD-L1) atezolizumab, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) ipilimumab, ICI-based combination TKIs, VEGF-neutralizing antibody or local therapies, are being further studied clinical trials. However, immune-related adverse events (irAEs) including cutaneous toxicity, gastrointestinal hepatotoxicity may lead termination ICI even threaten patients’ lives. This review aims summarize currently available immunotherapies introduce irAEs their managements order provide references application research.
Язык: Английский
Процитировано
18Cell Death Discovery, Год журнала: 2023, Номер 9(1)
Опубликована: Дек. 12, 2023
Cepharanthine (CEP), a bioactive compound derived from Stephania Cephalantha Hayata, is cytotoxic to various malignancies. However, the underlying mechanism of gastric cancer unknown. CEP inhibited cellular activity AGS, HGC27 and MFC cell lines in this study. CEP-induced apoptosis reduced Bcl-2 expression increased cleaved caspase 3, 9, Bax, Bad expression. caused G2 cycle arrest cyclin D1 cyclin-dependent kinases 2 (CDK2) Meanwhile, it oxidative stress, decreased mitochondrial membrane potential, enhanced reactive oxygen species (ROS) accumulation lines. Mechanistically, Kelch-like ECH-associated protein (Keap1) while activating NF-E2 related factor (Nrf2) nuclear translocations, increasing transcription Nrf2 target genes quinone oxidoreductase 1 (NQO1), heme oxygenase (HMOX1), glutamate-cysteine ligase modifier subunit (GCLM). Furthermore, combined analysis targeted energy metabolism RNA sequencing revealed that could alter levels metabolic substances such as D (+) - Glucose, D-Fructose 6-phosphate, citric acid, succinic pyruvic thereby altering AGS cells. In addition, significantly tumor growth BALB/c nude mice vivo, consistent with vitro findings. Overall, can induce stress by regulating Nrf2/Keap1 metabolism, resulting anti-gastric effects. Our findings suggest potential application treatment.
Язык: Английский
Процитировано
17International Journal of Biological Macromolecules, Год журнала: 2024, Номер 266, С. 130943 - 130943
Опубликована: Март 22, 2024
Язык: Английский
Процитировано
8International Immunopharmacology, Год журнала: 2024, Номер 129, С. 111601 - 111601
Опубликована: Фев. 13, 2024
Язык: Английский
Процитировано
7Medical Oncology, Год журнала: 2024, Номер 41(6)
Опубликована: Май 4, 2024
Язык: Английский
Процитировано
7Frontiers in Oncology, Год журнала: 2022, Номер 11
Опубликована: Янв. 26, 2022
Liver cancer is the third most common cause of cancer-related death following lung and stomach cancers. As a highly lethal disease, liver diagnosed frequently in less developed countries. Natural compounds extracted from herbs, animals natural materials have been adopted by traditional Chinese medicine (TCM) practices reported to be effective development new medications for treatment diseases. It important focus on mechanisms action against hepatocellular carcinoma (HCC), particularly terms cell cycle regulation, apoptosis induction, autophagy mediation migration invasion. In this review, we characterize novel representative according their pharmacologic effects based recently published studies. The aim review summarize explore therapeutic drug targets compounds, which could accelerate discovery anticancer drugs.
Язык: Английский
Процитировано
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