Non-Coding RNAs in Cancer: Mechanistic Insights and Therapeutic Implications DOI

Arjumand John,

Nuha Almulla,

Noureddine Elboughdiri

et al.

Pathology - Research and Practice, Journal Year: 2024, Volume and Issue: 266, P. 155745 - 155745

Published: Nov. 29, 2024

Language: Английский

Interactions between the metabolic reprogramming of liver cancer and tumor microenvironment DOI Creative Commons

Haoqiang Yang,

Jinghui Li, Yuanjie Niu

et al.

Frontiers in Immunology, Journal Year: 2025, Volume and Issue: 16

Published: Feb. 14, 2025

Metabolic reprogramming is one of the major biological features malignant tumors, playing a crucial role in initiation and progression cancer. The tumor microenvironment consists various non-cancer cells, such as hepatic stellate cancer-associated fibroblasts (CAFs), immune well extracellular matrix soluble substances. In liver cancer, metabolic not only affects its own growth survival but also interacts with other cells by influencing expression release metabolites cytokines (such lactate, PGE2, arginine). This interaction leads to acidification restricts uptake nutrients resulting competition symbiosis. At same time, neighboring during proliferation differentiation processes impacts immunity. article provides comprehensive overview crosstalk between cancer their microenvironment, deepening our understanding relevant findings pathways. contributes further regulation development evasion mechanisms while providing assistance advancing personalized therapies targeting pathways for anti-cancer treatment.

Language: Английский

Citations

1

Integrative pan-cancer analysis and experiment validation identified GLS as a biomarker in tumor progression, prognosis, immune microenvironment, and immunotherapy DOI Creative Commons
Dongming Li, Donghui Cao, Yangyu Zhang

et al.

Scientific Reports, Journal Year: 2025, Volume and Issue: 15(1)

Published: Jan. 2, 2025

Glutaminase (GLS), a crucial gene regulating glutaminolysis, has received much attention as it was found to regulate tumor metabolism and copper-induced cell death. However, its biological roles mechanisms in human cancers remain obscure. Consequently, the integrated pan-cancer analyses experiments were conducted elucidate oncological functions. We GLS differentially expressed upregulated predicted poor survival, clinicopathological progression, heterogeneity. Single-cell analysis closely related various functions pathways. Spatial transcriptomic expression mainly derived from cells, which implies cells may have stronger ability utilize glutamine than antitumor immune microenvironment (TME). Meanwhile, we noticed strongly infiltration of stromal immunomodulatory genes, activity some conventional agents, therapeutic response immunotherapy. Moreover, enrichment suggested metabolic reprogramming, innate adaptive immunity suppression, extracellular matrix remodeling. Finally, observed highly our gastric cancer (GC) cohort. As an independent risk factor for GC prognosis, high-GLS pathological progression. Inhibiting effectively prevented proliferation, migration, invasion triggered apoptosis. In conclusion, is underlying biomarker TME, drug sensitivity, immunotherapy response. Targeting can facilitate implementation individualized combined treatment strategies.

Language: Английский

Citations

0

Migrasome-related prognostic signature TSPAN4 correlates with immune infiltrates and metabolic disturbances in hepatocellular carcinoma DOI
Xiaoli Zhang, ­Jun Li­,

Yichen Yao

et al.

Journal of Gastroenterology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 12, 2025

Language: Английский

Citations

0

Diagnostic value of a lactylation-related gene signature in hepatocellular carcinoma DOI Open Access
Jiajia Zhang,

Chunmei Dong,

Lili Wu

et al.

Translational Cancer Research, Journal Year: 2025, Volume and Issue: 14(1), P. 296 - 312

Published: Jan. 1, 2025

The occurrence rate of liver cancer is increasing in recent years. significance lactylation tumor cells should not be neglected. This study aimed to discover a gene signature related that can used for diagnostic applications. Data were downloaded from Cancer Genome Atlas (TCGA), GSE14520, GSE84402, and GSE62232 datasets. Differential analysis random forest performed hepatocellular carcinoma (HCC). Receiver operating characteristic (ROC) curve was evaluate efficiency, logistic regression established obtain the risk score equation. Besides, expression genes identified by TCGA database verified real-time quantitative polymerase chain reaction (RT-PCR). In order analyze prognostic performance, patients diagnosed with HCC stratified into either high or low categories based on median score. addition, immunotherapy drug sensitivity groups assessed. performance model validated Gene Expression Omnibus (GEO) dataset. had worse outcomes than those database. ROC curves showed characteristics lactylation-related good predictive capability. Furthermore, we developed nomogram patients, utilizing data resources TCGA. Finally, terms assessing potency group lower Tumor Immune Dysfunction Exclusion (TIDE) score, indicating response immunotherapy. Our identification associated presents promising avenue development targeted immunotherapeutic strategies.

Language: Английский

Citations

0

Metabolic Reprogramming in Cholangiocarcinoma Cancer Stem Cells: Emerging Therapeutic Paradigms DOI
Qi Wang, Timothy E. Long, Peili Tang

et al.

Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217714 - 217714

Published: April 1, 2025

Language: Английский

Citations

0

Targeting PKLR in liver diseases DOI Creative Commons
Meng Yuan, Mengnan Shi, Hong Yang

et al.

Trends in Endocrinology and Metabolism, Journal Year: 2025, Volume and Issue: unknown

Published: April 1, 2025

Language: Английский

Citations

0

Fatty Acid Synthase Inhibitor Cerulenin Hinders Liver Cancer Stem Cell Properties through FASN/APP Axis as Novel Therapeutic Strategies DOI Creative Commons
Liang-Yun Chen,

Dao-Sian Wu,

Yao Shen

et al.

Journal of Lipid Research, Journal Year: 2024, Volume and Issue: 65(11), P. 100660 - 100660

Published: Sept. 26, 2024

Hepatocellular carcinoma (HCC) poses significant treatment challenges due to high postoperative recurrence rates and the limited effectiveness of targeted medications. Researchers have identified unique metabolic profiles cancer stem cells (CSCs) as primary drivers recurrence, metastasis, drug resistance. Therefore, address therapeutic conundrum, this study focused on rewinding reprogramming CSCs a novel strategy. HCC exhibited elevated fatty acid (FA) metabolism compared with parental cells. To specifically target FA in CSCs, we utilized cerulenin, synthase (FASN) inhibitor. Surprisingly, cerulenin can diminish CSC-like characteristics, including stemness gene expression, spherogenicity, tumorigenicity, metastatic potential. In addition, sorafenib, multikinase inhibitor used therapy for advanced HCC, was employed combination demonstrating great synergistic effect, particularly CSCs. Importantly, our RNA sequencing analysis disclosed that amyloid protein precursor (APP) is crucial downstream effector FASN regulating CSC properties. We found APP plays role CSCs' characteristics be inhibited by cerulenin. By focusing metabolism, FASN/APP axis viable develop more potent strategy HCC.

Language: Английский

Citations

3

Drug resistance in TKI therapy for hepatocellular carcinoma: mechanisms and strategies DOI
Xue Jiang,

Xiaoying Ge,

Yueying Huang

et al.

Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217472 - 217472

Published: Jan. 1, 2025

Language: Английский

Citations

0

Sweet dreams could be made of this: carbohydrate‐responsive element‐binding protein (ChREBP) as a target for hepatocellular carcinoma therapy DOI Creative Commons
Maite G. Fernández‐Barrena, Matías A. Ávila

Molecular Oncology, Journal Year: 2024, Volume and Issue: unknown

Published: June 4, 2024

Rewiring of cellular metabolism is now fully recognized as a hallmark cancer. Tumor cells reprogram metabolic pathways to meet the energetic and macromolecular demands support unrestricted growth survival under unfavorable conditions. It becoming apparent that these adaptations underpin most traits define cancer cell's identity, including ability avoid immune surveillance, endure nutrient oxygen restrictions, detach migrate from their natural histological niche, avert human‐made aggressions ( i.e. , therapy). In recent study, Benichou collaborators identify carbohydrate‐responsive element‐binding protein (ChREBP), master regulator physiological glucose metabolism, an oncogene in hepatocellular carcinoma (HCC) development. Upregulation ChREBP expression results self‐stimulatory loop interconnecting PI3K/AKT signaling feed fatty acid nucleotide synthesis supporting tumorigenesis. Importantly, pharmacological inhibition activity quells vivo HCC tumor without causing systemic toxicity. This study identifies novel oncometabolic open up new avenues improve treatment deadly tumor.

Language: Английский

Citations

0

Cancer metabolic reprogramming and precision medicine-current perspective DOI Creative Commons
Tingting Gao,

Liuxin Yang,

Yali Zhang

et al.

Frontiers in Pharmacology, Journal Year: 2024, Volume and Issue: 15

Published: Oct. 17, 2024

Despite the advanced technologies and global attention on cancer treatment strategies, continues to claim lives adversely affects socio-economic development. Although combination therapies were anticipated eradicate this disease, resilient restorative nature of cancers allows them proliferate at expense host immune cells energetically. This proliferation is driven by metabolic profiles specific type patient. An emerging field exploring reprogramming (MR) predict effective treatments. mini-review discusses recent advancements in MR that have contributed predictive, preventive, precision medicine. Current perspectives mechanisms various types prospects for personalized medicine are essential optimizing outputs necessary

Language: Английский

Citations

0