Evidence map›Paper›PMID 32021271›Full record

ArticleOncoTargets and therapy2020

LncRNA PVT1 Enhances Proliferation and Cisplatin Resistance via Regulating miR-194-5p/HIF1a Axis in Oral Squamous Cell Carcinoma.

Fang Wang, Xin Ji, Jingjing Wang, Xiangrui Ma, Yong Yang, Jinhua Zuo, Jun Cui

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
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  8. METTL3-mediated mAmerican journal of cancer research · 2025
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  12. lncRNA PVT1: a novel oncogene in multiple cancers.Cellular & molecular biology letters · 2022
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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

7 authors at 3 institutions in 1 country.

Fang WangDepartment of Oral and Maxillofacial Surgery, Binzhou Medical University Hospital, Binzhou 256603, People's Republic of China.
Xin JiDepartment of Pediatrics, Binzhou Medical University Hospital, Binzhou 256603, People's Republic of China.
Jingjing WangDepartment of Oral and Maxillofacial Surgery, Binzhou Medical University Hospital, Binzhou 256603, People's Republic of China.
Xiangrui MaDepartment of Oral and Maxillofacial Surgery, Binzhou Medical University Hospital, Binzhou 256603, People's Republic of China.
Yong YangDepartment of Oral and Maxillofacial Surgery, Binzhou Medical University Hospital, Binzhou 256603, People's Republic of China.
Jinhua ZuoDepartment of Oral and Maxillofacial Surgery, Binzhou Medical University Hospital, Binzhou 256603, People's Republic of China.
Jun CuiDepartment of Implant Dentistry, Jinnan Stomatological Hospital, Jinan 250001, People's Republic of China.
Binzhou Medical University · CNBinzhou University · CNJinan Stomatological Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOral squamous cell carcinoma (OSCC) is the most frequent oral malignancy. Recent studies have revealed that long non-coding RNA (lncRNA) PVT1 plays important roles in the pathogenesis of various cancers. However, the functional roles of PVT1 in OSCC progression and cisplatin resistance have not been elucidated. MATERIAL AND

methodsIn this study, PVT1 expression level in cisplatin-sensitive and cisplatin-resistant OSCC tissues and cell lines was determined using qRT-PCR. Gain-of-function and loss-of-function assays were performed to explore the biological roles of PVT1 in OSCC cell proliferation and cisplatin resistance. Western blot, luciferase reporter assay and bioinformatics analysis were employed to investigate the underlying mechanism of PVT1 in OSCC progression.

resultsHere, we found that PVT1 was frequently up-regulated in cisplatin-resistant tissues and cell lines and strongly correlated with worse overall survival. Functional studies showed that PVT1 promoted OSCC cell proliferation and cisplatin resistance. Mechanistic investigation revealed that PVT1 could positively regulate HIF1a expression via its competing endogenous RNA (ceRNA) activity on miR-194-5p. In addition, miR-194-5p conversely correlated with PVT1 and HIF1a expression in OSCC samples. More importantly, HIF1a knock-down or miR-194-5p overexpression reversed PVT1-induced promotion of OSCC cell proliferation and cisplatin resistance.

conclusionOur results indicated that PVT1 functions as an oncogene involved in OSCC cell proliferation and cisplatin-resistance and may serve as a novel therapeutic target for OSCC treatment.

Indexed as

cisplatin resistanceHIF1amiR-194-5poral squamous cell carcinoma

Identifiers

PMID32021271
PMCPMC6957095
OpenAlexW2999843446

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.