In vitro analysis of PI3K pathway activation genes for exploring novel biomarkers and therapeutic targets in clear cell renal carcinoma

被引:0
|
作者
Ali, Liaqat [1 ]
Raza, Abbas Ali [2 ]
Bin Zaheer, Ahmad [3 ]
Alhomrani, Majid [4 ,5 ]
Alamri, Abdulhakeem S. [4 ,5 ]
Alghamdi, Saleh A. [6 ]
Almalki, Abdulraheem Ali [7 ]
Alghamdi, Ahmad A. [8 ]
Khawaja, Imran [9 ]
Alhadrami, Mai [10 ]
Ramzan, Faiqah [11 ]
Jamil, Muhammad [12 ]
Ali, Mubarik [13 ]
Jabeen, Norina [14 ]
机构
[1] Inst Kidney Dis, Dept Urol, Hayatabad Med Complex, Peshawar 25000, Pakistan
[2] MTI Mardan Med Complex, Dept Surg, Bacha Khan Med Coll, Mardan 23200, Pakistan
[3] Basic Hlth Unit, Attock 43600, Pakistan
[4] Taif Univ, Ctr Biomed Sci Res CBSR, Deanship Sci Res, Taif 21944, Saudi Arabia
[5] Taif Univ, Fac Appl Med Sci, Dept Clin Lab Sci, Taif 21944, Saudi Arabia
[6] Taif Univ, Dept Clin Lab Since Med Genet, Coll Appl Med Sci, Taif 21944, Saudi Arabia
[7] Taif Univ, Dept Clin Lab Sci, Coll Appl Med Sci, Taif 21944, Saudi Arabia
[8] Taif Univ, Dept Clin Labs Sci, Coll Appl Med Sci, POB 11099, Taif 21944, Saudi Arabia
[9] Ayub Teaching Hosp, Dept Med, Abbottabad 22010, Pakistan
[10] Umm Alqura Univ, Dept Pathol, Fac Med, Mecca 24373, Saudi Arabia
[11] Gomal Univ, Fac Vet & Anim Sci, Dept Anim & Poultry Prod, Dera Ismail Khan 29050, Pakistan
[12] PARC Arid Zone Res Ctr, Dera Ismail Khan 29050, Pakistan
[13] Inst Anim Sci, Natl Agr Res Ctr, Islamabad 54000, Pakistan
[14] Univ Agr Faisalabad, Dept Rural Sociol, Faisalabad 38040, Pakistan
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2023年 / 15卷 / 07期
关键词
KIRC; immunotherapy; biomarker; hub gene; PREDICTION MODEL; WEB SERVER; CANCER; EXPRESSION; PTEN; PROGNOSIS; P53; METHYLATION; ROLES; STAGE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: The regulation of various cellular functions such as growth, proliferation, metabolism, and angiogenesis, is dependent on the PI3K pathway. Recent evidence has indicated that kidney renal clear cell carcinoma (KIRC) can be triggered by the deregulation of this pathway. The objective of this research was to investigate 25 genes associated with activation of the PI3K pathway in KIRC and control samples to identify four hub genes that might serve as novel molecular biomarkers and therapeutic targets for treating KIRC. Methods: Multi-omics in silico and in vitro analysis was employed to find hub genes related to the PI3K pathway that may be biomarkers and therapeutic targets for KIRC. Results: Using STRING software, a protein-protein interaction (PPI) network of 25 PI3K pathway-related genes was developed. Based on the degree scoring method, the top four hub genes were identified using Cytoscape's Cytohubba plug-in. TCGA datasets, KIRC (786-O and A-498), and normal (HK2) cells were used to validate the expression of hub genes. Additionally, further bioinformatic analyses were performed to investigate the mechanisms by which hub genes are involved in the development of KIRC. Out of a total of 25 PI3K pathway-related genes, we developed and validated a diagnostic and prognostic model based on the up-regulation of TP53 (tumor protein 53) and CCND1 (Cyclin D1) and the down-regulation of PTEN (Phosphatase and TENsin homolog deleted on chromosome 10), and GSK3B (Glycogen synthase kinase-3 beta) hub genes. The hub genes included in our model may be a novel therapeutic target for KIRC treatment. Additionally, associations between hub genes and infiltration of immune cells can enhance comprehension of immunotherapy for KIRC. Conclusion: We have created a new diagnostic and prognostic model for KIRC patients that uses PI3K pathway-related hub genes (TP53, PTEN, CCND1, and GSK3B). Nevertheless, further experimental studies are required to ascertain the efficacy of our model.
引用
收藏
页码:4851 / 4872
页数:22
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