Migrasome Marker Epidermal Growth Factor Domain-Specific O-GlcNAc Transferase: Pan-Cancer Angiogenesis Biomarker and the Potential Role of circ_0058189/miR-130a-3p/EOGT Axis in Hepatocellular Carcinoma Progression and Sorafenib Resistance DOI Creative Commons
Zhe Yu, Jing Luo, Wen An

и другие.

Biomedicines, Год журнала: 2025, Номер 13(4), С. 773 - 773

Опубликована: Март 22, 2025

Background: The EGF domain-specific O-GlcNAc transferase (EOGT), a migrasome marker, plays emerging roles in cancer biology through O-GlcNAcylation modifications, yet its pan-cancer functions and therapeutic implications remain underexplored. This study aimed to systematically characterize EOGT’s oncogenic mechanisms across malignancies, with particular focus on hepatocellular carcinoma (HCC) progression sorafenib resistance. Methods: Multi-omics analysis integrated TCGA/GTEx data from 33 types spatial/single-cell transcriptomics 10 HCC cohorts. Functional validation employed Huh7 cell models EOGT modulation, RNA sequencing, ceRNA network construction. Drug sensitivity leveraged GDSC/CTRP/PRISM databases, while immune microenvironment assessment utilized ESTIMATE/TIMER algorithms. Results: showed cancer-specific dysregulation, marked by significant upregulation correlating advanced stages poor survival. Pan-cancer revealed association genomic instability, tumor stemness, angiogenesis. Experimental demonstrated promotion of proliferation migration. A novel exosomal circ_0058189/miR-130a-3p/EOGT axis was identified, showing that circ_0058189 upregulated tissues, plasma samples exosomes sorafenib-resistant cells. Conclusion: establishes as angiogenesis biomarker, elucidating role resistance via circRNA-mediated regulation, providing mechanistic insights for targeted intervention strategies.

Язык: Английский

N-glycosylation of GSTO1 promotes cervical cancer migration and invasion through JAK/STAT3 pathway activation DOI
Panpan Yu,

Zouyu Zhao,

Qianyu Sun

и другие.

Functional & Integrative Genomics, Год журнала: 2025, Номер 25(1)

Опубликована: Март 3, 2025

Язык: Английский

Процитировано

0

Liver Metastasis in Cancer: Molecular Mechanisms and Management DOI Creative Commons
Wenchao Xu,

Jia Xu,

Jianzhou Liu

и другие.

MedComm, Год журнала: 2025, Номер 6(3)

Опубликована: Фев. 27, 2025

Abstract Liver metastasis is a leading cause of mortality from malignant tumors and significantly impairs the efficacy therapeutic interventions. In recent years, both preclinical clinical research have made significant progress in understanding molecular mechanisms strategies liver metastasis. Metastatic tumor cells different primary sites undergo highly similar biological processes, ultimately achieving ectopic colonization growth liver. this review, we begin by introducing inherent metastatic‐friendly features We then explore panorama conclude three continuous, yet distinct phases based on liver's response to This includes metastatic sensing stage, stress support stage. discuss intricate interactions between various resident recruited cells. addition, emphasize critical role spatial remodeling immune Finally, review advancements challenges faced management Future precise antimetastatic treatments should fully consider individual heterogeneity implement targeted interventions stages

Язык: Английский

Процитировано

0

The Role of Epithelial–Mesenchymal Transition in Osteosarcoma Progression: From Biology to Therapy DOI Creative Commons

Adriana Pătrașcu,

Elena Ţarcă, Ludmila Lozneanu

и другие.

Diagnostics, Год журнала: 2025, Номер 15(5), С. 644 - 644

Опубликована: Март 6, 2025

Osteosarcoma (OS) is the most common primary malignant bone tumor, predominantly affecting children, adolescents, and young adults. Epithelial-mesenchymal transition (EMT), a process in which epithelial cells lose their cell-cell adhesion gain migratory invasive properties, has been extensively studied various carcinomas. However, its role mesenchymal tumors like osteosarcoma remains less explored. EMT increasingly recognized as key factor progression of osteosarcoma, contributing to tumor invasion, metastasis, resistance chemotherapy. This narrative review aims provide comprehensive overview molecular mechanisms driving highlighting involvement signaling pathways such TGF-β, transcription factors Snail, Twist, Zeb, microRNAs modulating EMT. Furthermore, we discuss how correlates with poor prognosis therapy patients, emphasizing potential targeting for therapeutic intervention. Recent advancements understanding have opened new avenues treatment, including inhibitors combination therapies aimed at overcoming drug resistance. By integrating biological insights clinical implications, this underscores importance critical target.

Язык: Английский

Процитировано

0

Unravelling key signaling pathways for the therapeutic targeting of non-small cell lung cancer DOI

P. Chavan,

Ruchi Pandey,

BHEEMANAGOUDA O. PATIL

и другие.

European Journal of Pharmacology, Год журнала: 2025, Номер unknown, С. 177494 - 177494

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Migrasome Marker Epidermal Growth Factor Domain-Specific O-GlcNAc Transferase: Pan-Cancer Angiogenesis Biomarker and the Potential Role of circ_0058189/miR-130a-3p/EOGT Axis in Hepatocellular Carcinoma Progression and Sorafenib Resistance DOI Creative Commons
Zhe Yu, Jing Luo, Wen An

и другие.

Biomedicines, Год журнала: 2025, Номер 13(4), С. 773 - 773

Опубликована: Март 22, 2025

Background: The EGF domain-specific O-GlcNAc transferase (EOGT), a migrasome marker, plays emerging roles in cancer biology through O-GlcNAcylation modifications, yet its pan-cancer functions and therapeutic implications remain underexplored. This study aimed to systematically characterize EOGT’s oncogenic mechanisms across malignancies, with particular focus on hepatocellular carcinoma (HCC) progression sorafenib resistance. Methods: Multi-omics analysis integrated TCGA/GTEx data from 33 types spatial/single-cell transcriptomics 10 HCC cohorts. Functional validation employed Huh7 cell models EOGT modulation, RNA sequencing, ceRNA network construction. Drug sensitivity leveraged GDSC/CTRP/PRISM databases, while immune microenvironment assessment utilized ESTIMATE/TIMER algorithms. Results: showed cancer-specific dysregulation, marked by significant upregulation correlating advanced stages poor survival. Pan-cancer revealed association genomic instability, tumor stemness, angiogenesis. Experimental demonstrated promotion of proliferation migration. A novel exosomal circ_0058189/miR-130a-3p/EOGT axis was identified, showing that circ_0058189 upregulated tissues, plasma samples exosomes sorafenib-resistant cells. Conclusion: establishes as angiogenesis biomarker, elucidating role resistance via circRNA-mediated regulation, providing mechanistic insights for targeted intervention strategies.

Язык: Английский

Процитировано

0