Evidence map›Paper›PMID 38062234›Full record

ArticleMolecular biotechnology2024

Circ_0061140 Potentiates Clear Cell Renal Cell Carcinoma Progression Via the MicroRNA-126-5p/ADAM9 Axis.

Guang Jia, Dan Lv, Shaobin Ni

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Article in Molecular biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Guang Jia *Department of Urology Surgery, The First Affiliated Hospital of Harbin Medical University, No. 23, Youyou Street, Nangang District, Harbin, 150001, Heilongjiang, People's Republic of China. 813747@hrbmu.edu.cn.ORCID http://orcid.org/0009-0008-7006-8621
Dan Lv *Department of Anesthesia, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, Heilongjiang, People's Republic of China.
Shaobin NiDepartment of Urology Surgery, The First Affiliated Hospital of Harbin Medical University, No. 23, Youyou Street, Nangang District, Harbin, 150001, Heilongjiang, People's Republic of China.

Funding

Hospital Fund of the First Affiliated Hospital of Harbin Medical University No.2021M07
6 · The paper itself

Abstract

Circular RNAs (circRNAs) function as new cancer biomarkers, but the role of circ_0061140 remains unknown in clear cell renal cell carcinoma (ccRCC). Therefore, we aimed to validate the functions of circ_0061140 in ccRCC and its potential as a prognostic biomarker. At first, circ_0061140 expression in ccRCC tissues and cells was detected, and circ_0061140 was upregulated in ccRCC tissues (p < 0.0001) and cells (p < 0.0001). Patients with high expression of circ_0061140 had a worse prognosis (p < 0.05). Then, siRNA against circ_0061140 was transfected into Caki-1 and UT14 cells to explore its roles in the biological functions of ccRCC cells, and suppressing roles of downregulated circ_0061140 were observed in the cell growth of Caki-1 and UT14 cells (p < 0.01). Next, circ_0061140 was found to be a sponge of miR-126-5p, and ADAM9 was determined to be a target of miR-126-5p. Finally, functional rescue experiments were conducted to observe their roles in ccRCC cell growth. It was suggested that suppressed miR-126-5p or overexpressed ADAM9 induced cell proliferation and restricted cell apoptosis in ccRCC cells based on si-circ_0061140 (p < 0.01). Altogether, this study highlights that circ_0061140 plays an oncogenic role in ccRCC through modulation of the miR-126-5p/ADAM9 axis.

Indexed as

ADAM ProteinsCarcinoma, Renal CellCell ProliferationGene Expression Regulation, NeoplasticKidney NeoplasmsMembrane ProteinsMicroRNAsRNA, CircularApoptosisBiomarkers, TumorCell Line, TumorDisease ProgressionFemaleHumansMaleMiddle AgedADAM9 protein, humanADAM ProteinsBiomarkers, TumorMembrane ProteinsMicroRNAsMIRN126 microRNA, humanRNA, CircularADAM9ApoptosisCirc_0061140Clear cell renal cell carcinomaMicroRNA-126-5pProliferation

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.