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Research ArticleOriginal Article
Open Access

The expression and significance of long non-coding RNA ITGB2-AS1 in renal clear cell carcinoma

Wei Zhou, Zhi-Gang Liu and Lian-Qu Wang
Saudi Medical Journal January 2023, 44 (1) 19-28; DOI: https://doi.org/10.15537/smj.2023.44.1.20220533
Wei Zhou
From the School of Nursing and Health (Zhou), Henan University, from the Department of Orthopedic (Liu), and from the Department of Urinary Surgery (Wang), The First Affiliated Hospital of Henan University, Henan, China.
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Zhi-Gang Liu
From the School of Nursing and Health (Zhou), Henan University, from the Department of Orthopedic (Liu), and from the Department of Urinary Surgery (Wang), The First Affiliated Hospital of Henan University, Henan, China.
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Lian-Qu Wang
From the School of Nursing and Health (Zhou), Henan University, from the Department of Orthopedic (Liu), and from the Department of Urinary Surgery (Wang), The First Affiliated Hospital of Henan University, Henan, China.
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  • Figure 1
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    Figure 1

    - The expression of ITGB2-AS1 in kidney renal clear cell carcinoma (KIRC) and correlation with prognosis. A) The expression of ITGB2-AS1 in KIRC analyzed by gene expression profiling interactive analysis (GEPIA) database. B) The expression of ITGB2-AS1 in KIRC and adjacent tissues from 45 patients with KIRC was detected by real-time quantitative polymerase chain reaction. C) Survival analysis results of 515 KIRC patients retrieved from GEPIA database. D) The relationship between ITGB2-AS1 expression and overall survival of 45 KIRC patients was analyzed by Kaplan-Meier. *P-value of <0.05.

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    Figure 2

    - The effect of ITGB2-AS1 on the proliferation and apoptosis of kidney renal clear cell carcinoma (KIRC) cells. A) The expression of ITGB2-AS1 in human kidney-2 (HK-2) and KIRC cell lines (A498, 786-O, ACHN, and Caki-1), *p<0.05, versus HK-2 cell. B) The expression of ITGB2-AS1 in Caki-1 cell after transfected with siRNA-ITGB2-AS1, *p<0.05, versus the siRNA-NC group. C) The expression of ITGB2-AS1 in ACHN cell after transfected with pcDNA3.1-ITGB2-AS1, *p<0.05, versus the siRNA-NC group. D) The proliferation activity of Caki-1 cell after down-regulation of ITGB2-AS1. E) The proliferation activity of ACHN cell after up-regulation of ITGB2-AS1, *p<0.05, versus the Vector group. F) The apoptosis rate of Caki-1 cell after down-regulation of ITGB2-AS1, *p<0.05, versus the siRNA-NC group. G) The apoposis rate of ACHN cell after up-regulation of ITGB2-AS1, *p<0.05, versus the Vector group.

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    Figure 3

    - The effect of ITGB2-AS1 on invasion and migration abilities of kidney renal clear cell carcinoma (KIRC) cells. A) The invasion ability of Caki-1 cell after down-regulation of ITGB2-AS1, scale bar: 50 µm, *p<0.05, versus the siRNA-NC group. B) The invasion ability of ACHN cell after up-regulation of ITGB2-AS1, scale bar: 50 µm, *p<0.05, versus the Vector group. C) The migration ability of Caki-1 cell after down-regulation of ITGB2-AS1, scale bar: 100 µm, *p<0.05, versus the siRNA-NC group. D) The migration ability of ACHN cell after up-regulation of ITGB2-AS1, scale bar: 100 µm, *p<0.05, versus the Vector group.

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    Figure 4

    - ITGB2-AS1 targeted regulate miR-338-3p/epidermal growth factor receptor (EGFR) axis in kidney renal clear cell carcinoma (KIRC). A) The binding site of miR338-3p in the ITGB2-AS1 was predicted by LncBase Predicted v.2 and verified by dual luciferase reporter gene assay, *p<0.05, versus the miR-NC group. B) The binding site of miR-338-3p in 3’UTR of EGFR was predicted by Starbase 3.0 and verified by dual luciferase reporter gene assay, *p<0.05, versus the miR-NC group. C&D) The direct correlation between ITGB2-AS1 and miR-338-3p or miR-338-3p and EGFR, both in Caki and ACHN cells, were confirmed by RNA pull-down assay, *p<0.05, versus the Bio-NC group. E) The expression of miR-338-3p both in Caki and ACHN cells after down-regulation or up-regulation of ITGB2-AS1, *p<0.05, versus the siRNA-NC or Vector groups. F) The expression of EGFR protein both in Caki and ACHN cells after down-regulation or up-regulation of ITGB2-AS1, *p<0.05, versus the siRNA-NC or Vector groups.

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    Table 1

    - Relationship between ITGB2-AS1 expression and clinicopathological characteristics of kidney renal clear cell carcinoma patients.

    VariablesnITGB2-AS1Comparison
    Low expression group (n=19)High expression group (n=26)
    Gender
    Male2711 (57.9)16 (61.5)χ2=0.184
    Female188 (42.1)10 (38.5)p=0.668
    Age
    <652511 (57.9)14 (53.8)χ2=0.073
    ≥65208 (42.1)12 (46.1)p=0.787
    Smoking history
    No2913 (68.4)16 (61.5)χ2==0.227
    Yes166 (31.6)10 (38.5)p=0.634
    Tumor diameter (cm)
    <5279 (47.4)18 (66.7)χ2==2.186
    ≥51810 (52.6)8 (44.4)p=0.239
    TNM stage
    I/II2715 (78.9)12 (46.1)χ2==4.919
    III/IV184 (21.0)14 (53.8)p=0.035
    Fuhrman class
    I/II2414 (73.7)10 (38.5)χ2==6.910
    III/IV215 (26.3)16 (61.5)p=0.009
    Lymph node metastasis
    No2815 (78.9)13 (50.0)χ2==3.913
    Yes174 (21.0)13 (50.0)p=0.065

    Values are presented as numbers and precentages (%). TNM: tumor node metastasis

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    The expression and significance of long non-coding RNA ITGB2-AS1 in renal clear cell carcinoma
    Wei Zhou, Zhi-Gang Liu, Lian-Qu Wang
    Saudi Medical Journal Jan 2023, 44 (1) 19-28; DOI: 10.15537/smj.2023.44.1.20220533

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    The expression and significance of long non-coding RNA ITGB2-AS1 in renal clear cell carcinoma
    Wei Zhou, Zhi-Gang Liu, Lian-Qu Wang
    Saudi Medical Journal Jan 2023, 44 (1) 19-28; DOI: 10.15537/smj.2023.44.1.20220533
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    Keywords

    • kidney renal clear cell carcinoma
    • long non-coding RNA
    • ITGB2-AS1
    • miR-338-3p
    • EGFR

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