Long non-coding RNA LINC01232 promotes malignancy of prostate cancer through regulation of miR-181a-5p/IRS2 pathway: Ki-67 protein molecular structure and function

被引:0
|
作者
Li, Baisen [1 ]
Li, Huiying [2 ]
Cheng, Xiangming [3 ]
Fang, Yudong [4 ]
Liu, Zhe [4 ]
Zhao, Pei [5 ]
Jin, Li [6 ,7 ]
机构
[1] Univ Elect Sci & Technol China, Sichuan Clin Res Ctr Canc, Sichuan Canc Ctr, Sichuan Canc Hosp & Inst,Affiliated Canc Hosp,Dept, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Outpatient Dept, West China Hosp, Chengdu, Peoples R China
[3] Nanjing Univ Chinese Med, Affiliated Hosp, Jiangsu Prov Hosp Tradit Chinese Med, Dept Oncol, Nanjing, Peoples R China
[4] Shanghai TCM Integrated Hosp, Dept Vasc Dis, 230 Baoding Rd, Shanghai 200082, Peoples R China
[5] Univ Elect Sci & Technol China, Sichuan Canc Hosp & Inst, Sichuan Canc Ctr, Sch Med,Dept Intens Care Unit, 55 Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[6] Macau Univ Sci & Technol, Fac Med, Sch Pharm, Macau 999078, Peoples R China
[7] Macau Univ Sci & Technol, Lab Drug Discovery Nat Resources & Industrializat, Macau 999078, Peoples R China
关键词
Long non-coding RNA LINC01232; miR-181a-5p/IRS2; pathway; Prostate cancer; Ki-67; protein; Protein molecular structure; INHIBITS CELL-PROLIFERATION; POOR-PROGNOSIS; PROGRESSION; GROWTH; EXPRESSION; INVASION; CERNA;
D O I
10.1016/j.ijbiomac.2025.141817
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The expression level of long non-coding RNA (lncRNA), which functions in a manner similar to that of microrNA, has been confirmed to be closely associated with the regulatory network of multiple cancers. The primary focus of this particular research endeavor was to elucidate the mechanism of action of LINC01232 within the context of prostate cancer, specifically examining how it influences the proliferation of prostate cancer cells by interacting with the miR-181a-5p/IRS2 pathway. Additionally, the study aimed to delve deeper into the role of the Ki-67 protein within this intricate process. To assess the expression and localization of the Ki-67 protein in prostate cancer cells, researchers employed a combination of immunofluorescence and immunohistochemistry techniques. The expression level of Ki-67 protein decreased significantly after down-regulation of LINC01232, indicating that the cell proliferation activity was inhibited. Immunofluorescence and immunohistochemical experiments further confirmed that the expression of Ki-67 protein in prostate cancer cells was positively correlated with the expression of LINC01232.
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页数:15
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