Evidence map›Paper›PMID 38837682›Full record

ArticleCancer reports (Hoboken, N.J.)2024

LncRNA PVT1 facilitates the growth and metastasis of colorectal cancer by sponging with miR-3619-5p to regulate TRIM29 expression.

Zhenni Sun, Xutong Li, Yanyan Shi, Yasai Yao

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

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

4 authors.

Zhenni SunDepartment of Oncology, Qingdao Municipal Hospital, Medical College of Qingdao University Qingdao, Qingdao, Shandong, People's Republic of China.
Xutong LiDepartment of Oncology, Qingdao Municipal Hospital, Medical College of Qingdao University Qingdao, Qingdao, Shandong, People's Republic of China.ORCID 0000-0002-6864-9872
Yanyan ShiDepartment of Oncology, Qingdao women and children's Hospital, Qingdao, Shandong, People's Republic of China.
Yasai YaoDepartment of Medical oncology, Qingdao Fuwai Cardiovascular Hospital, Qingdao, Shandong, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is the second most common cause of cancer-related death worldwide. Long noncoding RNA (lncRNA) is involved in many malignant tumors. This study aimed to clarify the role of the lncRNA plasmacytoma variant translocation 1 (PVT1) in CRC growth and metastasis.

methodsDifferentially expressed lncRNAs in CRC were analyzed using the Cancer Genome Atlas. Gene expression profiling interactive analysis and a comprehensive resource for lncRNAs from cancer arrays databases were used to analyze lncRNA PVT1 expression and CRC prognosis, respectively. Cell counting kit-8, wound healing, colony formation, Transwell, and immunofluorescence assays were used to evaluate CRC cell proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT), respectively. Tumor growth and metastasis models were used to explore the PVT1 effect on the growth and metastasis of CRC in vivo.

resultsPVT1 was highly expressed in CRC, associated with a poor prognosis of CRC, and showed good diagnostic value. Transfection of sh-PVT1 or pcDNA3.1-PVT1 reduced or increased the proliferation, wound healing rate, colony formation, invasion, and EMT of CRC cells. PVT1 and miR-3619-5p were co-expressed in CRC cytoplasm, and PVT1 acted as a competitive endogenous RNA (ceRNA) by sponging miR-3619-5p to up-regulate tripartite motif containing 29 (TRIM29) expression. MiR-3619-5p overexpression and TRIM29 knockdown reduced proliferation, wound healing rate, invasion, and EMT of CRC cells. However, simultaneous PVT1 and miR-3619-5p overexpression or knockdown of miR-3619-5p and TRIM29 knockdown rescued the malignant phenotype of CRC cells.

conclusionsWe first clarified the ceRNA mechanism of PVT1 in CRC, which induced growth and metastasis by sponging with miR-3619-5p to regulate TRIM29.

Indexed as

Cell MovementCell ProliferationColorectal NeoplasmsGene Expression Regulation, NeoplasticMicroRNAsRNA, Long NoncodingAnimalsCell Line, TumorDNA-Binding ProteinsEpithelial-Mesenchymal TransitionFemaleHumansMaleMiceMice, Inbred BALB CMice, NudeDNA-Binding ProteinsMicroRNAsMIRN-3619 microRNA, humanPVT1 long-non-coding RNA, humanRNA, Long NoncodingTranscription FactorsTRIM29 protein, humancolorectal cancerepithelial‐mesenchymal transition (EMT)lncRNA plasmacytoma variant translocation 1 (PVT1)miR‐3619‐5ptripartite motif containing 29 (TRIM29)

Identifiers

PMID38837682
PMCPMC11150075

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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.