RETRACTED: AEG-1/miR-221 Axis Cooperatively Regulates the Progression of Hepatocellular Carcinoma by Targeting PTEN/PI3K/AKT Signaling Pathway (Retracted article. See vol. 23, 2022)

被引:20
|
作者
Kannan, Maheshkumar [1 ]
Jayamohan, Sridharan [1 ]
Moorthy, Rajesh Kannan [1 ]
Chabattula, Siva Chander [2 ]
Ganeshan, Mathan [3 ]
Arockiam, Antony Joseph Velanganni [1 ]
机构
[1] Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India
[2] Indian Inst Technol Madras, Bhupat & Jyoti Mehta Sch Biosci, Dept Biotechnol, Chennai 600036, Tamil Nadu, India
[3] Bharathidasan Univ, Sch Life Sci, Dept Biomed Sci, Canc Biol Lab, Tiruchirappalli 620024, Tamil Nadu, India
关键词
miR-221; astrocyte elevated gene-1; HCC; cell proliferation; regulatory proteins; FACTOR-KAPPA-B; ASTROCYTE ELEVATED GENE-1; CANCER CELLS; PROTEIN; PROLIFERATION; TRANSCRIPTION; ANGIOGENESIS; METASTASIS; EXPRESSION; ACTIVATION;
D O I
10.3390/ijms20225526
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
Hepatocellular carcinoma (HCC) is the third leading malignancy worldwide, causing mortality in children and adults. AEG-1 is functioned as a scaffold protein for the proper assembly of RNA-induced silencing complex (RISC) to optimize or increase its activity. The increased activity of oncogenic miRNAs leads to the degradation of target tumor suppressor genes. miR-221 is an oncogenic miRNA, that plays a seminal role in carcinogenesis regulation of HCC. However, the molecular mechanism and biological functions of the miR-221/AEG-1 axis have not been investigated extensively in HCC. Here, the expression of miR-221/AEG-1 and their target/associate genes was analyzed by qRT-PCR and Western blot. The role of the miR-221/AEG-1 axis in HCC was evaluated by proliferation assay, migration assay, invasion assay, and flow cytometry analysis. The expression level of miR-221 decreased in AEG-1 siRNA transfected HCC cells. On the other hand, there were no significant expression changes of AEG-1 in miR-221 mimic and miR-221 inhibitor transfected HCC cells and inhibition of miR-221/AEG-1 axis decreased cell proliferation, invasion, migration, and angiogenesis and induced apoptosis, cell cycle arrest by upregulating p57, p53, PTEN, and RB and downregulating LSF, MMP9, OPN, Bcl-2, PI3K, AKT, and LC3A in HCC cells. Furthermore, these findings suggest that the miR-221/AEG-1 axis plays a seminal oncogenic role by modulating PTEN/PI3K/AKT signaling pathway in HCC. In conclusion, the miR-221/AEG-1 axis may serve as a potential target for therapeutics, diagnostics, and prognostics of HCC.
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页数:18
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