Hsa_circ_0007718 facilitates the progression of colorectal cancer by regulating the miR-1299/PSMC2 axis

被引:0
|
作者
Wang, Yi [1 ]
Liu, Yanxia [2 ]
Wang, Yong [3 ]
Ren, Peng [1 ]
Tian, Hui [1 ]
Wang, Lin [1 ]
机构
[1] Shandong Univ, Cheeloo Coll Med, Qilu Hosp, Dept Radiat Oncol, Jinan, Peoples R China
[2] Shengli Oil Cent Hosp, Dept Oncol, Dongying, Peoples R China
[3] Feixian Peoples Hosp, Dept Gastrointestinal Surg, Linyi, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Colorectal cancer; hsa_circ_0007718; miR-1299; PSMC2; Proliferation; Migration; CIRCULAR RNA; PROLIFERATION; METASTASIS;
D O I
10.1016/j.ijbiomac.2024.136537
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
Colorectal cancer (CRC) represents one of the most prevalent forms of malignant tumors, characterized by a notably high rate of mortality among affected individuals. The primary objective of this investigation is to delve into the functional role of Hsa_circ_0007718 in the context of colorectal cancer and to elucidate its impact on the progression of CRC by modulating the interaction between the miR-1299 microRNA and its target gene, PSMC2. To assess the expression levels of Hsa_circ_0007718, along with miR-1299 and PSMC2, real-time quantitative fluorescent PCR (qRT-PCR) assays were meticulously performed using both CRC cell lines and clinical samples derived from patients. A cellular model was established to investigate the interactions occurring between miR1299 and Hsa_circ_0007718, as well as the connections to PSMC2, thereby providing a comprehensive understanding of these molecular interactions. The findings of this research revealed a significant upregulation of Hsa_circ_0007718 in both colorectal cancer cell lines and tissue samples. Importantly, the data indicated that the suppression of Hsa_circ_0007718 led to a marked decrease in the proliferation rates, migratory potential, and invasive capabilities of CRC cells. Furthermore, the study confirmed that Hsa_circ_0007718 acts as a downstream target of miR-1299, exerting its regulatory effects by inhibiting miR-1299 and thereby promoting the expression of PSMC2.
引用
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页数:11
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