Identification of significant hub genes and pathways associated with metastatic breast cancer and tolerogenic dendritic cell via bioinformatics analysis DOI

Kirstie Wong Chee Ching,

Noor Fatmawati Mokhtar, Gee Jun Tye

и другие.

Computers in Biology and Medicine, Год журнала: 2024, Номер 184, С. 109396 - 109396

Опубликована: Ноя. 16, 2024

Язык: Английский

Multi-Omics Profiling Identifies a High-Risk Subgroup of Breast Cancer Stem Cells for Prognostic Stratification and Personalized Treatment DOI Creative Commons
Guixin Wang, Ziyi Chen,

Yao Tian

и другие.

Journal of Cancer, Год журнала: 2025, Номер 16(6), С. 1860 - 1872

Опубликована: Фев. 28, 2025

Background: Breast cancer is the most prevalent malignancy among females worldwide. Extensive research has highlighted stem cells (CSCs) as critical drivers of tumor initiation, progression, recurrence, and therapy resistance. However, heterogeneity breast (BCSCs) their dynamic roles within microenvironment remain inadequately understood. Methods: This study utilized single-cell RNA sequencing dataset to categorize BCSCs into two subgroups investigate pseudo-time developmental dynamics. Bulk transcriptomic data from TCGA-BRCA were integrated assess prognostic significance infiltration abundance BCSCs-2 subgroup. Functional enrichment, co-expression network analysis, somatic mutation profiling performed elucidate key biological pathways genetic features. Additionally, drug sensitivity analyses conducted using Connectivity Map database identify potential therapeutic strategies. Results: A total 459 identified further classified distinct subpopulations: BCSCs-1 BCSCs-2. High was associated with poor prognosis an immunosuppressive microenvironment. Co-expression analysis 16 genes linked BCSCs-2, while revealed patterns its infiltration. Drug suggested that patients high could benefit classical chemotherapy agents, such Cisplatin, other novel compounds. Conclusions: offers insights functional in cancer. The findings highlight importance subgroup, providing biomarkers targets for precision medicine management.

Язык: Английский

Процитировано

1

The PTTG1/VASP axis promotes oral squamous cell carcinoma metastasis by modulating focal adhesion and actin filaments DOI Creative Commons
Suyeon Park,

Sang Shin Lee,

Shihyun Kim

и другие.

Molecular Oncology, Год журнала: 2025, Номер unknown

Опубликована: Янв. 10, 2025

The dynamics of focal adhesions (FAs) are essential physiological processes involved in cell spreading, metastasis, and regulation the actin cytoskeleton. FAs complex structures comprising proteins, such as paxillin zyxin, which interact with extracellular membranes influence motility morphology. Although related studies have been reported various cancers, function molecular mechanisms oral squamous carcinoma (OSCC) remain unknown. We investigated coordination between cytoskeleton FA specifically introducing pituitary tumor‐transforming gene 1 ( PTTG1 ; also known regulator sister chromatid separation, securin) into OSCC. Furthermore, we explored co‐localization several through small interfering RNA (siRNA) control or siRNA‐vasodilator‐stimulated phosphoprotein VASP ) ‐ , examining mediated by induced changes OSCC both vitro vivo . knockdown regulates dynamic cytoskeleton, restricting protrusion from front to rear cells. Our findings may provide new insights how cells each other on surface OSCC, influencing metastatic properties.

Язык: Английский

Процитировано

0

Prolonged Low-Dose Administration of FDA-Approved Drugs for Non-Cancer Conditions: A Review of Potential Targets in Cancer Cells DOI Open Access
Olivia Chang,

Sophia S. Cheon,

Nina Semenova

и другие.

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(6), С. 2720 - 2720

Опубликована: Март 18, 2025

Though not specifically designed for cancer therapy, several FDA-approved drugs such as metformin, aspirin, and simvastatin have an effect in lowering the incidence of cancer. However, there is a great discrepancy between vitro concentrations needed to eliminate cells plasma concentration normally tolerated within body. At present, no universal explanation this mechanisms been proposed including targeting stem (CSCs) or cellular senescence. CSCs are with ability self-renewal differentiation known be resistant chemotherapy. Senescence response damage stress, characterized by permanent cell-cycle arrest apoptotic resistance. Although, both situations, few examples where low were most effective, satisfactory data support that either senescence target these drugs. In review, we concisely summarize used non-cancer conditions well their potential action incidence. addition, propose prolonged low-dose administration (PLDA) specific can useful effectively preventing metastasis formation selected patients.

Язык: Английский

Процитировано

0

Application of mass cytometry in the immune microenvironment of breast cancer DOI

Yuefeng Shang,

Yuheng Pang,

Ying Liu

и другие.

Medical Oncology, Год журнала: 2025, Номер 42(6)

Опубликована: Май 19, 2025

Язык: Английский

Процитировано

0

FEN1 upregulation mediated by SUMO2 via antagonizing proteasomal degradation promotes hepatocellular carcinoma stemness DOI Creative Commons
Z. Peng,

Shuling Wang,

Diguang Wen

и другие.

Translational Oncology, Год журнала: 2024, Номер 44, С. 101916 - 101916

Опубликована: Март 20, 2024

Metastasis of hepatocellular carcinoma (HCC) critically impacts the survival prognosis patients, with pivotal role stem cells in initiating invasive metastatic behaviors. The Flap Endonuclease 1 (FEN1) is delineated as a metallonuclease, quintessential for myriad cellular processes including DNA replication, synthesis, damage rectification, Okazaki fragment maturation, baseexcision repair, and preservation genomic stability. Furthermore, it has been recognized an oncogene diverse range malignancies. Our antecedent research highlighted pronounced overexpression protein FEN1 carcinoma, where amplifies invasiveness potential liver cancer cells. However, its precise (LCSCs) remains enigma requires further investigation.

Язык: Английский

Процитировано

2

Identification of significant hub genes and pathways associated with metastatic breast cancer and tolerogenic dendritic cell via bioinformatics analysis DOI

Kirstie Wong Chee Ching,

Noor Fatmawati Mokhtar, Gee Jun Tye

и другие.

Computers in Biology and Medicine, Год журнала: 2024, Номер 184, С. 109396 - 109396

Опубликована: Ноя. 16, 2024

Язык: Английский

Процитировано

1