Pan-cancer analysis identifies venous thromboembolism-related genes F3, PLAT, and C1S as potential prognostic biomarkers for glioblastoma and lower grade glioma DOI Creative Commons
Jing Zhang, Qian Zhao, Yun Du

и другие.

Molecular Biomedicine, Год журнала: 2024, Номер 5(1)

Опубликована: Авг. 24, 2024

Abstract Venous thromboembolism (VTE) is a prevalent complication among patients with cancer, contributing significantly to morbidity and mortality. However, the relationship between VTE-related genes (VRGs) their potential impact on prognosis, immune response, therapeutic targets in various cancer types remains unclear. Based coagulation complement pathways, we identified hub VRGs that play role regulating response cancer. Specifically, factor III (F3), plasminogen activator (PLAT) C1s (C1S) were as exhibit high expression levels, positively correlating tumor stemness copy number variations, while inversely methylation particular types. Pan-cancer survival analysis revealed detrimental effects of these several types, notably glioblastoma lower grade glioma (GMBLGG). Further using receiver operating characteristic (ROC) curves demonstrated accuracy F3, PLAT C1S predicting outcomes GBMLGG, area under curve (AUC) values ranging from 0.78 0.9. Validation prognostic value three GMBLGG was conducted an independent Gene Expression Omnibus (GEO) dataset. Additionally, gene–drug association ciclosporin, ouabain 6- mercaptopurine, which all immunosuppressive properties, options for exhibiting or expression, respectively. In summary, our findings provide bioinformatics perspective pan-cancer, highlighting pivotal roles C1S, could potentially be therapeutically exploited targeted cancers, especially GBMLGG.

Язык: Английский

Integrative Analysis of Transcriptomic Data Reveals a Predictive Gene Signature for Chemoradiotherapy Response in Rectal Cancer DOI

Claudia Corro apos,

Joao Victor Machado Carvalho,

Melivoia Rapti

и другие.

Опубликована: Янв. 1, 2025

BackgroundLocally advanced rectal cancer (LARC) is treated with neoadjuvant chemoradiotherapy (nCRT) followed by surgery, achieving pathological complete response (pCR) in ~15% of cases. Enhancing pCR through combined nCRT and chemotherapy increases toxicity, while many patients fail to benefit from nCRT, experiencing significant side effects. Predicting could enable non-surgical management via a watch-and-wait strategy spare non-responders unnecessary toxicity. However, no gene expression signatures predicting have yet been clinically implemented.MethodsWe conducted differential analysis across six GEO datasets integrated four microarray refine findings. Using machine learning, we developed signature predictive validated it cross-validation. Gene set enrichment (GSEA) identified biological pathways linked response. Spatial transcriptomic profiling using GeoMx Digital Profiling (DSP) technology was performed on pre-treatment biopsies uncover compartment-specific markers within tumor stroma.ResultsThe achieved strong performance (AUC = 0.80) GLMnet Random Forest models significantly associated consensus molecular subtypes (CMS4) immune (iCMS3). GSEA revealed related VEGFR, EGFR, Toll-like receptor signaling. transcriptomics eight genes, tumor-associated genes showing higher value than stroma-associated markers.ConclusionWe present novel LARC potential guide personalized treatment. highlights the microenvironment's contribution therapy outcomes, warranting further validation larger cohorts.

Язык: Английский

Процитировано

0

Alternative Splicing at the Crossroad of Inflammatory Bowel Diseases and Colitis-Associated Colon Cancer DOI Open Access
Paulo Matos, Peter Jordan

Cancers, Год журнала: 2025, Номер 17(2), С. 219 - 219

Опубликована: Янв. 11, 2025

The risk of developing colorectal cancer (CRC) is increased in ulcerative colitis patients compared to the general population. This results from state chronic inflammation, a well-known tumour-promoting condition. review explores pathologic and molecular characteristics colitis-associated colon (CAC), emphasizing distinct features sporadic CRC. We focus on key signalling pathways involved transition CAC, highlighting emerging role alternative splicing these processes, namely how inflammation-induced can significantly contribute CRC observed among UC patients. calls for more transcriptomic studies elucidate mechanisms through which drives CAC pathogenesis. A better understanding events crucial as they may reveal novel biomarkers disease progression have potential target changes therapeutic strategy.

Язык: Английский

Процитировано

0

Colorectal Cancer: Current and Future Therapeutic Approaches and Related Technologies Addressing Multidrug Against Multiple Level Resistance Mechanisms DOI Open Access

Marianna Puzzo,

Marzia De Santo,

Catia Morelli

и другие.

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(3), С. 1313 - 1313

Опубликована: Фев. 4, 2025

Colorectal cancer (CRC) is the third most common and associated with a poor prognosis. The mutation profile related involved pathways of CRC have been, in broad terms, analyzed. main current therapeutic approaches been comprehensively reviewed here, future possible therapeu-tic options technologies perspectively presented. complex scenario represented by multiple-level resistance mechanism epidermal growth factor receptor (EGFR) pathway, including mutations KRAS, NRAS, BRAF V600E, discussed. Examples engineered from literature along drug combination tested clinical trials are encouraging results observed latter (the BEACON trial), totally free chemotherapy, prompted authors to imagine nanotechnology-assisted approach for bypassing mechanisms, hopefully allowing, principle, complete biological remission.

Язык: Английский

Процитировано

0

Identification of SRC, AKT1 and MAPK3 as Therapeutic Targets of Apigenin and Luteolin in Colorectal and Colon Carcinoma through Network Pharmacology DOI Creative Commons
Kha Wai Hon, Sagnik Nag,

B. Stany

и другие.

Food Bioscience, Год журнала: 2025, Номер unknown, С. 106313 - 106313

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Eudragit S 100 Assisted Molecular Solid Dispersion of Andrographolide Tendered Augmented Drug Delivery and Apoptosis in Human Colon Cancer, HT-29 Cells DOI
Pawan Devangan, Anamika Sharma,

Nitin Wadate

и другие.

AAPS PharmSciTech, Год журнала: 2025, Номер 26(3)

Опубликована: Март 11, 2025

Язык: Английский

Процитировано

0

Pan-cancer analysis identifies venous thromboembolism-related genes F3, PLAT, and C1S as potential prognostic biomarkers for glioblastoma and lower grade glioma DOI Creative Commons
Jing Zhang, Qian Zhao, Yun Du

и другие.

Molecular Biomedicine, Год журнала: 2024, Номер 5(1)

Опубликована: Авг. 24, 2024

Abstract Venous thromboembolism (VTE) is a prevalent complication among patients with cancer, contributing significantly to morbidity and mortality. However, the relationship between VTE-related genes (VRGs) their potential impact on prognosis, immune response, therapeutic targets in various cancer types remains unclear. Based coagulation complement pathways, we identified hub VRGs that play role regulating response cancer. Specifically, factor III (F3), plasminogen activator (PLAT) C1s (C1S) were as exhibit high expression levels, positively correlating tumor stemness copy number variations, while inversely methylation particular types. Pan-cancer survival analysis revealed detrimental effects of these several types, notably glioblastoma lower grade glioma (GMBLGG). Further using receiver operating characteristic (ROC) curves demonstrated accuracy F3, PLAT C1S predicting outcomes GBMLGG, area under curve (AUC) values ranging from 0.78 0.9. Validation prognostic value three GMBLGG was conducted an independent Gene Expression Omnibus (GEO) dataset. Additionally, gene–drug association ciclosporin, ouabain 6- mercaptopurine, which all immunosuppressive properties, options for exhibiting or expression, respectively. In summary, our findings provide bioinformatics perspective pan-cancer, highlighting pivotal roles C1S, could potentially be therapeutically exploited targeted cancers, especially GBMLGG.

Язык: Английский

Процитировано

0