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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Axis Cooperatively Regulates the Progression of Hepatocellular Carcinoma by Targeting PTEN/PI3K/AKT Signaling Pathway (Retracted article.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
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Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India

Jayamohan, Sridharan
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Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India

Moorthy, Rajesh Kannan
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Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India

Chabattula, Siva Chander
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Indian Inst Technol Madras, Bhupat & Jyoti Mehta Sch Biosci, Dept Biotechnol, Chennai 600036, Tamil Nadu, India Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India

Ganeshan, Mathan
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Bharathidasan Univ, Sch Life Sci, Dept Biomed Sci, Canc Biol Lab, Tiruchirappalli 620024, Tamil Nadu, India Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India

Arockiam, Antony Joseph Velanganni
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Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India Bharathidasan Univ, Sch Life Sci, Dept Biochem, Mol Oncol Lab, Tiruchirappalli 620024, Tamil Nadu, India
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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