Therapeutic Potential of CPPs DOI
Ülo Langel

Springer eBooks, Journal Year: 2023, Volume and Issue: unknown, P. 407 - 467

Published: Jan. 1, 2023

Language: Английский

Advances in the roles of ATF4 in osteoporosis DOI Open Access
Yaosheng Xiao,

Xunlu Xie,

Zhixi Chen

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2023, Volume and Issue: 169, P. 115864 - 115864

Published: Nov. 9, 2023

Osteoporosis (OP) is characterized by reduced bone mass, decreased strength, and enhanced fragility fracture risk. Activating transcription factor 4 (ATF4) plays a role in cell differentiation, proliferation, apoptosis, redox balance, amino acid uptake, glycolipid metabolism. ATF4 induces the differentiation of marrow mesenchymal stem cells (BM-MSCs) into osteoblasts, increases osteoblast activity, inhibits osteoclast formation, promoting formation remodeling. In addition, mediates energy metabolism osteoblasts promotes angiogenesis. also involved mediation adipogenesis. can selectively accumulate osteoblasts. directly interact with RUNT-related 2 (RUNX2) up-regulate expression osteocalcin (OCN) osterix (Osx). Several upstream factors, such as Wnt/β-catenin BMP2/Smad signaling pathways, have been ATF4-mediated differentiation. osteoclastogenesis mediating receptor activator nuclear κ-B (NF-κB) ligand (RANKL) signaling. agents, parathyroid (PTH), melatonin, natural compounds, reported to regulate mediate this review, we comprehensively discuss biological activities maintaining homeostasis inhibiting OP development. has become therapeutic target for treatment.

Language: Английский

Citations

23

Engineered human osteoarthritic cartilage organoids DOI Creative Commons

Laura Dönges,

Atharva Damle, Andrea Mainardi

et al.

Biomaterials, Journal Year: 2024, Volume and Issue: 308, P. 122549 - 122549

Published: March 22, 2024

The availability of human cell-based models capturing molecular processes cartilage degeneration can facilitate development disease-modifying therapies for osteoarthritis (Acevedo Rua et al., 2021) [1], a currently unmet clinical need. Here, by imposing specific inflammatory challenges upon mesenchymal stromal cells at defined stage chondrogenesis, we engineered organotypic model which recapitulates main OA pathological traits such as chondrocyte hypertrophy, matrix mineralization, enhanced catabolism and mechanical stiffening. To exemplify the utility model, exposed organoids to factors known attenuate features, including IL-1Ra, carried out mass spectrometry-based proteomics. We identified that IL-1Ra strongly reduced production transcription factor CCAAT/enhancer-binding protein beta (Hirata 2012) [2] demonstrated inhibition C/EBPβ-activating kinases could revert degradative processes. Human thus represent relevant tool towards discovery new drivers assessment therapeutics targeting associated pathways.

Language: Английский

Citations

11

Applications of cell penetrating peptide-based drug delivery system in immunotherapy DOI Creative Commons
Jingjing Du, Ruyan Zhang, Shuqi Jiang

et al.

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

Published: Jan. 22, 2025

Cell penetrating peptides (CPPs) are usually positive charged and have good cell membrane permeability. Meanwhile, CPPs facile to synthesize, can be functionalized satisfy different demands, such as cyclization, incorporating unnatural amino acids, lipid conjugation. These properties made them efficient drug-delivery tools deliver therapeutic molecules cells tissues in a nontoxic manner, including small molecules, DNA, siRNA, proteins other various nanoparticles. However, the poor serum stability low tumor targeting ability also hindered their broad application. Besides, inappropriate chemical modification lead disruption nonspecific toxicity. In this paper, we first reviewed recent advances CPP applications for cancer therapy via covalent or non-covalent manners. We carefully analyzed advantages disadvantages of each modifications drug delivery. Then, concluded progress clinical trials diseases. Finally, discussed challenges opportunities met translate into applications. This review presented new insight delivery, which could provide advice on design clinically effective systemic delivery systems using CPPs.

Language: Английский

Citations

0

Transcription Factor CEBPD-Mediated WTAP Facilitates the Stemness, Growth, Migration and Glycolysis of Glioblastoma Stem Like Cells DOI

Jiong Geng,

Yun Shao,

Yi Pu

et al.

Neurochemical Research, Journal Year: 2025, Volume and Issue: 50(2)

Published: Feb. 13, 2025

Language: Английский

Citations

0

Radiological and Immunohistochemical Characteristics of PitNETs in 79 Patients Undergoing Neurosurgery DOI Open Access
Anna Krzentowska, Ryszard Czepko, Dariusz Adamek

et al.

Cancers, Journal Year: 2025, Volume and Issue: 17(4), P. 666 - 666

Published: Feb. 16, 2025

The human pituitary is a gland located within small bony box, the sella turcica, under base of brain [...]

Language: Английский

Citations

0

IGH rearrangements in Down syndrome acute lymphoblastic leukemia DOI Creative Commons

Naomi Michels,

Jade Admiraal,

Aurélie Boeree

et al.

EJC Paediatric Oncology, Journal Year: 2025, Volume and Issue: unknown, P. 100223 - 100223

Published: Feb. 1, 2025

Language: Английский

Citations

0

Basic biology and roles of CEBPD in cardiovascular disease DOI Creative Commons

T Li,

Shaoling Lin, Ying Zhu

et al.

Cell Death Discovery, Journal Year: 2025, Volume and Issue: 11(1)

Published: March 14, 2025

Abstract CCAAT/enhancer-binding protein delta (CEBPD), as an evolutionarily conserved in mammals, belongs to the CEBP transcription factor family, which modulates many biological processes. The diversity of CEBPD functions partly depends on cell type and cellular context. Aberrant expression activity are associated with multiple organ diseases, including cardiovascular diseases. In this review, we describe basic molecular biology understand its regulation, modifications, functions. Here, summarize recent advances genetically modified animals CEBPD. Finally, discuss contribution diseases highlight strategies for developing novel therapies targeting

Language: Английский

Citations

0

TMEM71 is crucial for cell proliferation in lower-grade glioma and is linked to unfavorable prognosis DOI Creative Commons

Jiabao Xie,

Wanli Yu,

Shikai Gui

et al.

Cancer Cell International, Journal Year: 2025, Volume and Issue: 25(1)

Published: March 21, 2025

Transmembrane protein 71 (TMEM71) is implicated in multiple cellular physiological functions and has been demonstrated to be crucial the advancement of different cancerous growths. However, its specific function low-grade glioma (LGG) remains unclear. We examined expression patterns prognostic importance TMEM71 various types cancer by using pan-cancer analysis. The analyses correlations between clinicopathological characteristics, prognosis, biological functions, immune genomic variations LGG were conducted based on patterns. Finally, level verified executing vitro studies. Abnormal elevation was associated with poor prognosis many tumors including LGG. Both multivariate univariate Cox regression indicated that served as a standalone biomarker for levels immune-related infiltration cells, checkpoint genes (ICPGs) expression, tumor mutation burden (TMB) patients In laboratory studies, elevated found involved activating JAK2/STAT3 pathway, promoting CCAAT/Enhancer Binding Protein D (CEBPD) ultimately affecting growth motility cells. an independent indicator strongly positioning it potential novel target treatment.

Language: Английский

Citations

0

HDAC4 Super-Enhancer Drives CEBPB-Mediated TWIST2 Transcription to Promote Chemoresistance in LUAD DOI

Min Jiang,

Kai Zhang,

Guohao Wei

et al.

Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217716 - 217716

Published: April 1, 2025

Language: Английский

Citations

0

COL1A1-positive endothelial cells promote gastric cancer progression via the ANGPTL4-SDC4 axis driven by Endothelial-to-Mesenchymal Transition DOI Creative Commons
Quanzhong Liu, Miao Yu, Zihan Lin

et al.

Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217731 - 217731

Published: April 1, 2025

Language: Английский

Citations

0