PRKD3 promotes proliferation of liver cancer cells: a downstream proteomics profiling study DOI
Ye Tian,

Bei Xie,

Shuaiyang Wang

и другие.

American Journal of Translational Research, Год журнала: 2024, Номер 16(11), С. 6384 - 6398

Опубликована: Янв. 1, 2024

Protein kinase D 3 (PRKD3), a serine/threonine protein kinase, functions as crucial regulator across numerous cancer types. However, its regulatory function and mechanism in hepatocellular carcinoma (HCC) proliferation remain unclear. In vitro experiments proteomics analysis offer new insights into the regulation of PRKD3 HCC. A knockdown cell line was constructed to assess effects on HCC cells using counting kit-8 (CCK-8) assay, 5-Ethynyl-2'-deoxyuridine (EdU) clonogenic flow cytometry. Proteomic changes liver before after were analyzed 4D-lablefree technology. Analysis The Cancer Genome Atlas (TCGA) dataset revealed abnormal expression HCC, associated with poorer prognosis specific pathological Results from CCK-8 assay showed marked reduction Huh7 (P < 0.01), number clonal colonies being 5.26 times higher than that cells, EdU positivity rate decreased 54.77% 37.97%. Flow cytometry results indicated knockout induced cycle arrest at G2/M phase. 330 proteins had altered expression, amino acid transport, stress response, apoptosis. Cyclin-dependent 4 (CDK4), plasminogen activator inhibitor 1 (SERPINE1), sequestosome (SQSTM1), ras-related Rab-8A (RAB8A), nuclear receptor-binding factor 2 (NRBF2) emerged key nodes interaction network. This study elucidates inhibitory effect unveils proteomic features regulation. CDK4, SERPINE1, SQSTM1, RAB8A, NRBF2 may serve PRKD3's pathways.

Язык: Английский

Development of endosome-related gene signature for the prediction of prognosis and therapeutic response in breast cancer DOI Creative Commons
Guowei Jiang, Ye Wang

Medicine, Год журнала: 2025, Номер 104(2), С. e41230 - e41230

Опубликована: Янв. 10, 2025

Endosomes play a pivotal role in cellular biology, orchestrating processes such as endocytosis, molecular trafficking, signal transduction, and recycling of materials. This study aims to construct an endosome-related gene (ERG)-derived risk signature for breast cancer prognosis. Transcriptomic clinical data were retrieved from The Cancer Genome Atlas the University California Santa Cruz databases build validate model. A Lasso Cox regression model was employed construction. immune landscape assessed using CIBERSORT ESTIMATE algorithms, while drug sensitivity evaluated via pRRophetic algorithm. Gene set enrichment analysis variation applied evaluate expression patterns. nomogram constructed validated predicting outcomes. ERGs cells tissues further validated. Sixty-one associated with prognosis identified, 23 selected constructing signature. stratified patients into high- low-risk groups, where group exhibited significantly better Notably, younger tended have lower scores compared older ones. enhanced majority drugs tested, accompanied by increased infiltration T M1 macrophages. Additionally, cell cycle pathways suppressed group, whereas antigen binding functions activated. Ultimately, score age identified independent prognostic factors cancer, these incorporated that demonstrated excellent performance assessment. Finally, external cohort dysregulation score-associated tissues. successfully established ERG-derived nomogram, elucidating their potential value prediction evaluation therapeutic response.

Язык: Английский

Процитировано

0

Genes Associated with the Immune System Affected by Ionizing Radiation and Estrogen in an Experimental Breast Cancer Model DOI Creative Commons
Gloria M. Calaf, Debasish Roy, Lilian Jara

и другие.

Biology, Год журнала: 2024, Номер 13(12), С. 1078 - 1078

Опубликована: Дек. 20, 2024

Breast cancer is a global health issue that, when in the metastasis stage, characterized by lack of estrogen receptor-α, progesterone receptor, and human epidermal growth receptor expressions. The present study analyzed differential gene expression related to immune system affected ionizing radiation cell lines derived from an experimental breast model that was previously developed; where immortalized epithelial line MCF-10F, triple-negative line, exposed low doses high linear energy transfer α particle (150 keV/μm), it subsequently grew presence or absence 17β-estradiol. Results indicated interferon-related developmental regulator 1 estrogen-treated line; this interferon, as well Interferon-Induced Transmembrane protein 2, TNF alpha-induced Protein 6 levels were higher than control Alpha3 line. Furthermore, 1, 6, Nuclear Factor Interleukin 3-regulated, Interferon-Gamma Receptor showed Alpha5 Interferon Regulatory Tumor2 Additionally, further strengthen these data, publicly available datasets analyzed. This analysis conducted assess correlation between alpha genes mentioned above patients, tumor normal tissues, infiltration level, ER status, survival outcome adjusted clinical stage factor. It can be concluded interferon family Tumor Necrosis factors potential therapeutic targets for cancer, since they are active before formation defense body under effects.

Язык: Английский

Процитировано

0

Affinity of PET-MRI Tracers for Hypoxic Cells in Breast Cancer: A Systematic Review DOI Creative Commons
Ioana-Claudia Costin, Loredana G. Marcu

Cells, Год журнала: 2024, Номер 13(12), С. 1048 - 1048

Опубликована: Июнь 17, 2024

Tumour hypoxia is a known microenvironmental culprit for treatment resistance, tumour recurrence and promotion of metastatic spread. Despite the long-known existence this factor within milieu, still one greatest challenges in cancer management. The transition from invasive less reliable detection methods to more accurate non-invasive ways identify quantify was long process that eventually led promising results showed by functional imaging techniques. Hybrid imaging, such as PET-CT, has great advantage combining structural or anatomical image (offered CT) with metabolic PET). However, context hypoxia, it only PET taken after appropriate radiotracer administration would supply hypoxia-specific information. To overcome limitation, development latest hybrid systems, PET-MRI, enables synergistic approach towards both having potential provide information on microenvironment. This study designed systematic review literature newest developments PET-MRI hypoxic cells breast cancer. analysis includes affinity various tracers patient group well correlations between PET-specific MRI-specific parameters, offer broader view widespread clinical implementation technique.

Язык: Английский

Процитировано

0

Morphological assessment of angiogenesis factor expression in tumor and microenvironment of breast fibroadenoma and ductal carcinoma: An observational cohort study DOI Creative Commons
K. A. Aliev, Eliza Asanova, Tatiana P. Makalish

и другие.

Kuban Scientific Medical Bulletin, Год журнала: 2024, Номер 31(5), С. 26 - 40

Опубликована: Окт. 25, 2024

Background . Angiogenesis plays a crucial role in the progression of breast cancer. Identifying and investigating key components this process, focused on phenotype as well microenvironment tumor, is considered highly relevant for understanding tumor biology. Studies into expression angiogenesis-related factors by means immunohistochemical methods appear valuable both assessing conventional chemotherapy options identifying new targets targeted therapy Objectives To investigate angiogenesis ductal carcinoma vascular endothelial growth factor, angiopoietin-2, hypoxia-inducible factor alpha context various therapeutic strategies. Methods An observational cohort study was conducted using biopsy samples from female patients with confirmed diagnoses “fibroadenoma” “ductal breast,” residents Republic Crimea, who applied to oncological hospitals Simferopol January 2021 2023. Examination involved histological sections tissue 68 verified carcinoma” (the mean age 65 ± 5). The following cohorts were formed study: control group, consisting fibroadenoma ( n = 20); two subgroups 48), including Group I — had not received 23), II breast, underwent surgery one or more courses 25). examining obtained paraffin blocks, markers via immunohistochemistry primary antibodies against angiopoietin 2, alpha. Statistical analysis carried out Statistica 10.0 (StatSoft, USA). Differences significant at error probability p ≤ 0.05. value < 0.05 deemed statistically all types analysis. Results differed significantly between groups when compared group. having cytoplasmic localization detected group benign processes, whereas nuclear noted groups. Significant differences have been established among breast: II, which chemotherapy, notably higher stroma tumor-free areas. greater demarcation zone than that observed surgically treated women 0.033; 0.034, 0.001, respectively). In epithelium carcinoma, expressed intensively did receive other 0.001). Conversely, stroma, exhibited levels those no treatment; areas due cell involvement 0.004) conditionally healthy regions represented patients, studied pronounced breast. Conclusion data indicate activation processes after evidenced increased angiopoietin. This result associated high prevalence resistant forms II. signaling pathways its provides insights patterns occurrence strategies overcome resistance

Язык: Английский

Процитировано

0

DNA Damage and Inflammatory Response of p53 Null H358 Non-Small Cell Lung Cancer Cells to X-Ray Exposure Under Chronic Hypoxia DOI Open Access
Hasan Nisar, Melanie Brauny,

Frederik M. Labonté

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(23), С. 12590 - 12590

Опубликована: Ноя. 23, 2024

Hypoxia-induced radioresistance limits therapeutic success in cancer. In addition, p53 mutations are widespread tumors including non-small cell lung carcinomas (NSCLCs), and they might modify the radiation response of hypoxic tumor cells. We therefore analyzed DNA damage inflammatory chronically (1% O

Язык: Английский

Процитировано

0

PRKD3 promotes proliferation of liver cancer cells: a downstream proteomics profiling study DOI
Ye Tian,

Bei Xie,

Shuaiyang Wang

и другие.

American Journal of Translational Research, Год журнала: 2024, Номер 16(11), С. 6384 - 6398

Опубликована: Янв. 1, 2024

Protein kinase D 3 (PRKD3), a serine/threonine protein kinase, functions as crucial regulator across numerous cancer types. However, its regulatory function and mechanism in hepatocellular carcinoma (HCC) proliferation remain unclear. In vitro experiments proteomics analysis offer new insights into the regulation of PRKD3 HCC. A knockdown cell line was constructed to assess effects on HCC cells using counting kit-8 (CCK-8) assay, 5-Ethynyl-2'-deoxyuridine (EdU) clonogenic flow cytometry. Proteomic changes liver before after were analyzed 4D-lablefree technology. Analysis The Cancer Genome Atlas (TCGA) dataset revealed abnormal expression HCC, associated with poorer prognosis specific pathological Results from CCK-8 assay showed marked reduction Huh7 (P < 0.01), number clonal colonies being 5.26 times higher than that cells, EdU positivity rate decreased 54.77% 37.97%. Flow cytometry results indicated knockout induced cycle arrest at G2/M phase. 330 proteins had altered expression, amino acid transport, stress response, apoptosis. Cyclin-dependent 4 (CDK4), plasminogen activator inhibitor 1 (SERPINE1), sequestosome (SQSTM1), ras-related Rab-8A (RAB8A), nuclear receptor-binding factor 2 (NRBF2) emerged key nodes interaction network. This study elucidates inhibitory effect unveils proteomic features regulation. CDK4, SERPINE1, SQSTM1, RAB8A, NRBF2 may serve PRKD3's pathways.

Язык: Английский

Процитировано

0