Evidence map›Paper›PMID 34236145›Full record

ArticleThoracic cancer2021

Overexpression of hsa_circ_0008274 inhibited the progression of lung adenocarcinoma by regulating HMGA2 via sponging miR-578.

Maolong Wang, Minge Ma, Yuling Yang, Chuan Li, Yuanyong Wang, Xiao Sun, Mengdi Wang, Yong Sun, Wenjie Jiao

Abstract read
In one paragraph

Article in Thoracic cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Maolong WangDepartment of Thoracic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0003-1284-852X
Minge MaDepartment of Radiology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Yuling YangDepartment of Infectious diseases, The Affiliated Hospital of Qingdao University, Qingdao, China.
Chuan LiDepartment of Thoracic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.
Yuanyong WangDepartment of Thoracic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0002-7753-8736
Xiao SunDepartment of Thoracic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.
Mengdi WangDepartment of Pharmacology, School of Pharmacy, Qingdao University, Qingdao, China.
Yong SunDepartment of Pharmacology, School of Pharmacy, Qingdao University, Qingdao, China.
Wenjie JiaoDepartment of Thoracic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCircular RNAs (circRNAs) had been identified as a non-coding RNA associated with many types of cancer in recent years. However, the involvement of hsa_circ_0008274 in lung adenocarcinoma (LUAD) has not been explored. The aim of our research is to explore the biological mechanism and function of hsa_circ_0008274 in LUAD.

methodsThe hsa_circ_0008274, miR-578, and high mobility group AT-Hook 2 (HMGA2) mRNA expression levels were detected via qRT-PCR. Cell Counting Kit-8 (CCK-8) Transwell assay and wound healing assay were performed to measure the cell proliferation, invasion, and migration ability. Luciferase reporter and Western blotting experiments were performed to characterize the competing endogenous RNA (ceRNA) mechanism of hsa_circ_0008274.

resultsOur findings determined that the expression of hsa_circ_0008274 in LUAD was significantly decreased. Cell experiments showed that overexpressed hsa_circ_0008274 could reduce the proliferation and invasion ability of LUAD cells. Moreover, miRNA-578 could identify as a miRNA sponge of hsa_circ_0008274. Overexpressed hsa_circ_0008274 reduced the proliferation and invasion of LUAD cells caused by miR-578 mimics. Increasing the expression of miR-578 can aggravate the proliferation and invasion of LUAD cells and block the inhibition of proliferation and invasion of LUAD cells mediated by overexpressed hsa_circ_0008274. Subsequent data indicate that HMGA2 of the tumor-promoting gene is the target gene of miR-578. The upregulation of HMGA2 partially reversed the tumor inhibitory effect of LUAD cells induced by overexpressed hsa_circ_0008274 or miR-578 mimics.

conclusionsIn summary, our data show that the overexpression of hsa_circ_0008274 repressed the proliferation and invasion of LUAD through downregulating miR-578 and activating HMGA2.

Indexed as

A549 CellsAdenocarcinoma of LungCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticHMGA2 ProteinHumansLung NeoplasmsMicroRNAsRNA, CircularHMGA2 ProteinHMGA2 protein, humanMicroRNAsRNA, CircularHMGA2hsa_circ_0008274lung adenocarcinomamiR-578

Identifiers

PMID34236145
PMCPMC8364990

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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.