ADAMTS7 Enhances Gastric Cancer Growth and Metastasis by Triggering the NF-κB Signaling Pathway DOI Creative Commons
Shun Chen,

Jiancheng He,

Hanxu Gao

et al.

Journal of Cancer, Journal Year: 2024, Volume and Issue: 16(3), P. 1008 - 1019

Published: Dec. 31, 2024

The ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family of metalloproteinases plays a vital role in various biological pathological processes, including tissue remodeling, angiogenesis, cancer progression.Among the 19 members, our research focused on ADAMTS7, which exhibited significant overexpression gastric (GC).This was strongly correlated poor clinical outcomes, reduced overall survival heightened metastatic potential.To investigate ADAMTS7 GC, we employed an integrated approach encompassing bioinformatics analysis, Western blotting, immunofluorescence, as well vitro vivo functional analyses.Our results showed that silencing expression significantly inhibited proliferation, migration, invasion GC cells, furthermore, growth metastasis tumour cells nude mice, highlighting its critical driving malignant behaviour cells.Further mechanistic studies identified NF-κB signaling pathway key downstream target resulting notable reduction activity.These findings establish contributor to aggressiveness pivotal activator pathway, major regulator inflammation tumor progression.Consequently, emerges promising therapeutic prognostic biomarker for GC.Our study opens new avenues development targeted therapies aimed at inhibiting activity, thereby potentially improving treatment outcomes rates patients GC.

Language: Английский

Advancements in the ERK1/2 Signaling Pathway Affecting Male Reproduction DOI Creative Commons
Yikuan Du,

Xianhong Chi,

Y Wang

et al.

Frontiers in Bioscience-Landmark, Journal Year: 2024, Volume and Issue: 29(1), P. 23 - 23

Published: Jan. 18, 2024

Male infertility, age-related changes, and tumors have been increasingly studied in the field of male reproductive health due to emergence environmental stressors, declining fertility rates, aging populations. Numerous studies demonstrated that ERK1/2 signaling pathway plays a significant role reproduction. The is associated with several pathways has complex interplay influences spermatogenic microenvironment, sperm viability, gonadal axis regulation, as well resistance testicular tumors. Moreover, directly or indirectly regulates somatic cells, which are crucial for maintaining spermatogenesis microenvironment regulation. Given critical health, comprehensive exploration its multifaceted effects on reproduction underlying mechanisms necessary. This study aims provide solid foundation in-depth research further enhance males.

Language: Английский

Citations

6

Cellular and molecular mechanisms of gastrointestinal cancer liver metastases and drug resistance DOI

Daosong Dong,

Yu Xue, Jingjing Xu

et al.

Drug Resistance Updates, Journal Year: 2024, Volume and Issue: 77, P. 101125 - 101125

Published: Aug. 6, 2024

Language: Английский

Citations

6

Unveiling ADAMTS12: A Key Driver of Bladder Cancer Progression via COL3A1-Mediated Activation of the FAK/PI3K/AKT Signaling Pathway DOI Creative Commons
Jianhua Xiao, Li‐zhe Xu,

Jinzhuo Ning

et al.

Journal of Biological Chemistry, Journal Year: 2025, Volume and Issue: 301(2), P. 108155 - 108155

Published: Jan. 4, 2025

Language: Английский

Citations

0

High-Grade Sarcomatous Transformation of Hybrid Hemosiderotic Fibrolipomatous Tumor-Myxoinflammatory Fibroblastic Sarcoma with Novel ADAMTS12::TERT Gene Fusion DOI Creative Commons
Jatin Gandhi, Kristin K. Deeb, Eleanor Y. Chen

et al.

International Journal of Surgical Pathology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 7, 2025

Hemosiderotic fibrolipomatous tumor (HFLT) and myxoinflammatory fibroblastic sarcoma (MIFS) are rare, locally aggressive soft tissue tumors with a predilection for distal extremities of middle-aged adults. Hybrid (HFLT-MIFS) demonstrate overlapping features both share recurrent translocation (1;10) (p22; q24). We describe high-grade sarcomatous transformation hybrid HFLT-MIFS, novel ADAMTS12::TERT gene fusion, presenting as right foot mass in an 85-year-old woman. Histologically, the showed areas HFLT-MIFS subsequent resection. The patient was treated surgically below-knee amputation interval radiation therapy. On RNA-based next-generation sequencing, harbored fusion. In addition to reporting fusion rare example transformation, we also discuss relevant morphological HFLT provide brief review reported neoplasms TERT fusions.

Language: Английский

Citations

0

The impact of ADAMTS14 genetic polymorphisms and its function on susceptibility to and prognosis of gastric cancer in a Chinese Han population DOI
Pengyu Li,

Jiacheng Dong,

Yuan Li

et al.

Gastric Cancer, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 24, 2025

Language: Английский

Citations

0

Targeting tumor extracellular matrix with nanoparticles to circumvent therapeutic resistance DOI
Xinyi Ding, Yiyu Liang, Siyuan Zhou

et al.

Journal of Controlled Release, Journal Year: 2025, Volume and Issue: unknown, P. 113786 - 113786

Published: April 1, 2025

Language: Английский

Citations

0

Dysregulation of autophagy in gastric carcinoma: Pathways to tumor progression and resistance to therapy DOI
Wen Wen, Yavuz Nuri Ertaş, Ahmet Erdem

et al.

Cancer Letters, Journal Year: 2024, Volume and Issue: 591, P. 216857 - 216857

Published: April 5, 2024

Language: Английский

Citations

3

The E3 ubiquitin ligase MAEA promotes macrophage phagocytosis and inhibits gastrointestinal cancer progression by mediating PARP1 ubiquitination and degradation DOI Creative Commons

Yanchun Feng,

Xiangcai Zou,

Jintuan Huang

et al.

International Journal of Biological Sciences, Journal Year: 2025, Volume and Issue: 21(4), P. 1784 - 1800

Published: Feb. 10, 2025

Background: While a role for the E3 ubiquitin ligase MAEA (macrophage erythroblast attacher) has been reported in several cancer types, its importance and mechanistic functions gastrointestinal (GIC) have yet to be established. Methods: The of GIC were explored through vitro vivo experiments, including loss- gain-of-function analyses. Mass spectrometry was used identify proteins that interact with MAEA. mechanisms which influences tumor aggression examined immunoprecipitation Results: patients exhibiting reduced expression found exhibit worse disease-free overall survival outcomes. impair proliferation chemoresistance tumors subcutaneous xenograft model systems. combination PARP1 inhibitor veliparib resulted enhanced oxaliplatin treatment efficacy vivo. From perspective, mediate K48-linked ubiquitination degradation PARP1, addition suppressing M2 polarization macrophages enhancing macrophage phagocytic activity. Conclusions: These data suggest offers value as prognostic biomarker target owing ability degrade augment activity macrophages.

Language: Английский

Citations

0

An emerging role of N-glycosylation in cancer chemoresistance DOI

Yuhan Sun,

Tiangui Wu,

Jianguo Gu

et al.

Carbohydrate Research, Journal Year: 2024, Volume and Issue: 539, P. 109107 - 109107

Published: April 9, 2024

Language: Английский

Citations

2

Parecoxib inhibits tumorigenesis and angiogenesis in hepatocellular carcinoma through ERKVEGF/MMPs signaling pathway DOI

Li Tian,

Y Huang, Yan Liu

et al.

IUBMB Life, Journal Year: 2024, Volume and Issue: unknown

Published: June 14, 2024

Abstract Parecoxib, a well‐recognized nonsteroidal anti‐inflammatory drug, has been reported to possess anticancer properties in various tumor types. In this work, we aimed investigate the potential effects of parecoxib on hepatocellular carcinoma (HCC) cells. To assess impact HCC cell proliferation, employed Cell Counting Kit‐8, colony formation, and 5‐ethynyl‐2′‐deoxyuridine assays. Hoechst/propidium iodide (PI) double staining flow cytometry were performed evaluate apoptosis cycle analysis. Wound healing transwell assays utilized migration invasion. Tube formation assay was analyze angiogenesis. Protein levels determined using western blotting, mRNA expression assessed quantitative real‐time polymerase chain reaction (PCR). A xenograft mouse model used confirm antitumor tumors vivo. Our data demonstrated that effectively inhibited proliferation cells dose‐ time‐dependent manner. addition, induced arrest G2 phase promoted apoptosis. Moreover, hindered invasion by impeding epithelial–mesenchymal transition process. Further investigation showed could significantly suppress angiogenesis through inhibition extracellular signal‐regulated kinase (ERK)–vascular endothelial growth factor (VEGF) axis. Notably, treatment with ERK activator phorbol myristate acetate upregulated matrix metalloproteinase (MMP)‐2, MMP‐9, VEGF reversed function Besides, displayed its efficacy Collectively, our results suggest ameliorates progression regulating cycle, apoptosis, migration, invasion, ERK–VEGF/MMPs signaling pathway.

Language: Английский

Citations

2