Evidence map›Paper›PMID 34307152›Full record

ArticleFrontiers in oncology2021

Long Noncoding RNA DICER1-AS1 Functions in Methylation Regulation on the Multi-Drugresistance of Osteosarcoma Cells

Feng Wang, Lingsuo Kong, Youguang Pu, Fengmei Chao, Chunbao Zang, Wei Qin, Fangfang Zhao, Shanbao Cai

Abstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 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

8 authors.

Feng WangDepartment of Oncology, The First Affiliated Hospital of University of Science and Technology of China (USTC), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Lingsuo KongDepartment of Anesthesiology, West district of The First Affiliated Hospital of USTC, Division of life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Youguang PuDepartment of Cancer Epigenetics Program, Anhui Provincial Cancer Hospital, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Fengmei ChaoDepartment of Cancer Epigenetics Program, Anhui Provincial Cancer Hospital, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Chunbao ZangDepartment of Radiation Oncology, Anhui Provincial Cancer Hospital, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Wei QinDepartment of Science and Education Section, Anhui Provincial Cancer Hospital, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Fangfang ZhaoDepartment of Cancer Epigenetics Program, Anhui Provincial Cancer Hospital, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Shanbao CaiDepartment of Orthopedic Surgery, Anhui Provincial Cancer Hospital, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is a common malignant bone tumor that commonly occurs in children and adolescents. Long noncoding RNAs (lncRNAs) are recognized as a novel class of regulators of gene expression associated with tumorigenesis. However, the effect and mechanism of lncRNAs in OS tumorigenesis and drug resistance have not been characterized. The purpose of the study is to screen potential biomarker and therapeutic target against OS. We compared the lncRNA expression profiles between OS cell lines with different drug resistance levels using RNA-seq analysis and found that lncRNA DICER1-AS1 was significantly differentially expressed in multi-drugresistant OS cells SJSA-1 versus multi-drugsensitive OS cells G-292. Bisulfite Sequencing PCR (BSP) assay was performed to analyze the differential methylation status of the promoter region of DICER1-AS1 in four OS cells. Subsequently,

Indexed as

DICER1-AS1drug resistanceGADD45AmiR-34a-5posteosarcoma

Identifiers

PMID34307152
PMCPMC8299526

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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.