Evidence map›Paper›PMID 35992869›Full record

ArticleFrontiers in oncology2022

LncRNA SCAMP1 disrupts the balance between miR-26a-5p and ZEB2 to promote osteosarcoma cell viability and invasion.

Rong Li, Zhen Chen, Yubo Zhou, Gulikezi Maimaitirexiati, Qi Yan, Yuting Li, Adilijiang Maimaitiyimin, Changhui Zhou, Jingqin Ren, Chengqing Liu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. 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
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Osteosarcoma in a ceRNET perspective.Journal of biomedical science · 2024
    Review
  5. Cancers · 2024
    Review
  6. Review
  7. Article
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

13 authors at 3 institutions in 1 country.

Rong LiCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Zhen ChenCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Yubo ZhouDepartment of Orthopedics, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, China.
Gulikezi MaimaitirexiatiCAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Qi YanCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Yuting LiCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Adilijiang MaimaitiyiminDepartment of Orthopedics, Xinjiang Medical University Affiliated Fifth Hospital, Urumqi, China.
Changhui ZhouCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Jingqin RenCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Chengqing LiuCollege of Public Health, Xinjiang Medical University, Urumqi, China.
Abasi MainikeDepartment of Orthopedics, Xinjiang Medical University Affiliated Fifth Hospital, Urumqi, China.
Peng ZhouDepartment of Orthopedics, Xinjiang Medical University Affiliated Fifth Hospital, Urumqi, China.
Lu DingTraditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Postdoctoral Research Center on Public Health and Preventive Medicine, Xinjiang Medical University, Xinjiang, China.
Xinjiang Medical University · CNFifth Affiliated Hospital of Xinjiang Medical University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma often occurs in children and adolescents and affects their health. The survival rate of osteosarcoma patients is unsatisfactory due to the lack of early detection and metastasis development and drug resistance. Hence, dissection of molecular insight into osteosarcoma initiation and progression is pivotal to provide the new therapeutic strategy. In recent years, long noncoding RNAs (lncRNAs) have burst into stage in osteosarcoma development and malignant behaviors. LncRNA SCAMP1 has been discovered to play an essential role in carcinogenesis and progression. However, the mechanisms of lncRNA SCAMP1-involved tumorigenesis have not been reported in human osteosarcoma. In this study, we utilized multiple cellular biological approaches to determine the function of lncRNA SCAMP1 in osteosarcoma cells. Moreover, we performed several molecular biological approaches to define the mechanism by which lncRNA SCAMP1 regulated cell viability and invasion in osteosarcoma. We dissected that lncRNA SCAMP1 promoted progression of osteosarcoma

Indexed as

invasionmiR-26a-5pSCAMP1viabilityZEB2

Identifiers

PMID35992869
PMCPMC9382636
OpenAlexW4289544927

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.