Evidence map›Paper›PMID 30652414›Full record

ArticleCancer medicine2019

Long noncoding RNA DNAJC3-AS1 promotes osteosarcoma progression via its sense-cognate gene DNAJC3.

Ridong Liang, Zezheng Liu, Zhixu Chen, Yang Yang, Yuejun Li, Zhifei Cui, Ajuan Chen, Zhenxue Long, Jinbin Chen, Jiachun Lu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. MiR-140 Targets lncRNA DNAJC3-AS1 to Suppress Cell Proliferation in Acute Myeloid Leukemia.Mediterranean journal of hematology and infectious diseases · 2022
    Article
  3. Article
  4. Long Non-coding RNAs in Cisplatin Resistance in Osteosarcoma.Current treatment options in oncology · 2021
    Review
  5. Article
  6. Article
  7. Article
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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

12 authors at 3 institutions in 1 country.

Ridong LiangDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Zezheng LiuDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Zhixu ChenDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Yang YangDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Yuejun LiDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Zhifei CuiDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Ajuan ChenDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Zhenxue LongDepartment of Orthopedics, The People's Hospital of Baise, Baise, China.
Jinbin ChenThe First Affiliated Hospital, The School of Public Health, The Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, China.
Jiachun LuThe First Affiliated Hospital, The School of Public Health, The Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, China.
Bin HuangDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.
Qingchu LiDepartment of Orthopedics, The Third Affiliated Hospital, Academy of Orthopedics, Southern Medical University, Guangzhou, China.ORCID 0000-0002-5221-0195
Third Affiliated Hospital of Southern Medical University · CNFirst Affiliated Hospital of Guangzhou Medical University · CNBaise University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs have been proved to play essential roles in tumor development and progression. In this study, we focused on DNAJC3-AS1 and investigated its biological function and clinical significance in osteosarcoma. We detected the expression of DNAJC3-AS1 in 30 pairs of matched osteosarcoma and adjacent nontumorous specimens and osteosarcoma cell lines and analyzed association between DNAJC3-AS1 levels and clinicopathological factors. We found that DNAJC3-AS1 expression was up-regulated in osteosarcoma. High level of DNAJC3-AS1 was correlated with high differentiated degree (P = 0.018) and advanced Enneking stage (P = 0.016). Mechanistically, DNAJC3-AS1 enhanced cell proliferation, migration, and invasion in vitro and in vivo and reduced sensitivity of osteosarcoma to cisplatin. These effects of DNAJC3-AS1 were reversed by down-regulation of its sense-cognate gene DNAJC3. Thus, DNAJC3-AS1 promotes osteosarcoma development and progression by regulating DNAJC3 and might be a biomarker and therapeutic target for osteosarcoma.

Indexed as

AdultAnimalsBone NeoplasmsCell Line, TumorDisease ProgressionFemaleHSP40 Heat-Shock ProteinsHumansMaleMice, Inbred BALB CMice, NudeOsteosarcomaPrognosisRNA, Long NoncodingUp-RegulationYoung AdultDNAJC3 protein, humanHSP40 Heat-Shock ProteinsRNA, Long NoncodingcisplatinDNAJC3-AS1eIF2αmetastasisosteosarcomaproliferation

Identifiers

PMID30652414
PMCPMC6382712
OpenAlexW2910677961

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.