Exploring the role of glucose‑6‑phosphate dehydrogenase in cancer

R Li, W Wang, Y Yang, C Gu - Oncology reports, 2020 - spandidos-publications.com
Abstract Glucose‑6‑phosphate dehydrogenase (G6PD) is a cytoplasmic enzyme found in
human erythrocytes that provides reduced NADPH for cell metabolism. Glutathione …

Suppression of macrophages-Induced inflammation via targeting RAS and PAR-4 signaling in breast cancer cell lines

NA Thabet, N El-Guendy, MM Mohamed… - Toxicology and applied …, 2019 - Elsevier
Tumor associated macrophages (TAMs) have a crucial role in cancer progression,
metastasis and drug response. Piroxicam and sulindac sulfide are non-steroidal anti …

Evidence of direct interaction between cisplatin and the caspase‐cleaved prostate apoptosis response‐4 tumor suppressor

KK Raut, S Pandey, G Kharel, SM Pascal - Protein Science, 2024 - Wiley Online Library
Abstract Prostate apoptosis response‐4 (Par‐4) tumor suppressor protein has gained
attention as a potential therapeutic target owing to its unique ability to selectively induce …

[引用][C] Heat shock protein 90α inhibitor, PU-H71 in combination with DHEA promoting apoptosis in triple-negative breast cancer cell line MDA-MB-231

H Soudan, H Saeed, M Eldemellawy… - Acta Biochimica …, 2020 - ojs.ptbioch.edu.pl
Due to the lack of markers (ER, PR, and HER-2/Neu) for the molecular-targeted therapies
triple-negative breast cancer (TNBC) is more challenging than other subtypes of breast …

Prostate apoptosis response-4: A therapeutic target for malignant gliomas

J Ghosalkar, V Sonawane, M Khan, K Joshi… - Tumor Suppressor Par-4 …, 2021 - Springer
Gliomas are the most common type of primary brain tumors and glioblastoma (GBM), the
most lethal of gliomas accounts for more than 60% of all brain tumors in adults. Despite the …

[HTML][HTML] Deciphering the Role of the Barr Body in Malignancy: An insight into head and neck cancer

D Sharma, G Koshy, S Gupta, B Sharma… - Sultan Qaboos …, 2017 - ncbi.nlm.nih.gov
X chromosome inactivation is the epitome of epigenetic regulation and long non-coding
ribonucleic acid function. The differentiation status of cells has been ascribed to X …

Analysis of Comparative Proteomic and Potent Targets of Peniciketal A in Human Acute Monocytic Leukemia

X Gao, Y Zhou, H Sun, D Liu, J Zhang… - Anti-Cancer Agents …, 2019 - ingentaconnect.com
Background: Peniciketal A (Pe-A), a spiroketal compound, shows potent anticancer activities
in human acute monocytic leukemia. However, the detailed mechanisms and potent targets …

Structural Insights into the cl-Par-4 Protein: Ionic Requirements, Conformational Transitions, and Interaction With Cisplatin

KK Raut - 2023 - digitalcommons.odu.edu
Cancer continues to be the leading global cause of death, with challenges in early
diagnosis, drug resistance, non-specific drug targeting, and cancer recurrence and …

PAR-4 选择性诱导肿瘤细胞凋亡机制的研究进展

郭雅馨, 孔庆宏, 王冠林 - 中国细胞生物学学报, 2017 - cqvip.com
在肿瘤治疗中, 寻找选择性作用于肿瘤细胞的药物是人们所期待和向往的. 前列腺凋亡反应蛋白-
4 (prostate apoptosis response protein-4, Par-4) 作为肿瘤抑制因子, 能选择性诱导肿瘤细胞凋 …

[PDF][PDF] ناطرسلا في راب مسلجا رود زومر كف

D Sharma, G Koshy, S Gupta, B Sharma, S Grover - academia.edu
: X chromosome inactivation is the epitome of epigenetic regulation and long
non-coding ribonucleic acid function. The differentiation status of cells has been ascribed to …