Evidence map›Paper›PMID 28771075›Full record

ArticleCell cycle (Georgetown, Tex.)2017

S-phase kinase-associated protein 2 promotes cell growth and motility in osteosarcoma cells.

Lu Ding, Rong Li, Rongxin Sun, Yang Zhou, Yubo Zhou, Xiaoping Han, Yong Cui, Wu Wang, Qing Lv, Jingping Bai

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

10 authors at 2 institutions in 1 country.

Lu Dinga Department of Orthopedics , Fifth Affiliated Hospital, Xinjiang Medical University , Xinjiang , China.
Rong Lic Department of Maternal , Child and Adolescent Health, College of Public Health, Xinjiang Medical University , Xinjiang , China.
Rongxin Sund Department of Orthopedics , Sixth Affiliated Hospital, Xinjiang Medical University , Xinjiang , China.
Yang Zhoub Department of Orthopedics , Tumor Hospital Affiliated to Xinjiang Medical University , Xinjiang , China.
Yubo Zhoue Department of Orthopedics , Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University , Xinjiang , China.
Xiaoping Hana Department of Orthopedics , Fifth Affiliated Hospital, Xinjiang Medical University , Xinjiang , China.
Yong Cuia Department of Orthopedics , Fifth Affiliated Hospital, Xinjiang Medical University , Xinjiang , China.
Wu Wanga Department of Orthopedics , Fifth Affiliated Hospital, Xinjiang Medical University , Xinjiang , China.
Qing Lva Department of Orthopedics , Fifth Affiliated Hospital, Xinjiang Medical University , Xinjiang , China.
Jingping Baib Department of Orthopedics , Tumor Hospital Affiliated to Xinjiang Medical University , Xinjiang , China.
Xinjiang Medical University · CNTumor Hospital of Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skp2 (S-phase kinase-associated protein 2) plays an oncogenic role in a variety of human cancers. However, the function of Skp2 in osteosarcoma (OS) is elusive. Therefore, in the current study, we explore whether Skp2 exerts its oncogenic function in OS. The cell growth, apoptosis, invasion and cell cycle were measured in OS cells after Skp2 overexpression. We found that overexpression of Skp2 enhanced cell growth, and inhibited cell apoptosis in OS cells. Moreover, we observed that upregulation of Skp2 accelerated cell cycle progression in OS cells. Furthermore, the ability of migration and invasion was enhanced in Skp2 overexpressing OS cells. Mechanically, our Western blotting data suggested that Skp2 decreased the expression of E-cadherin, Foxo1, p21, and p57, but increased MMP-9 in OS cells. In conclusion, our study demonstrated that Skp2 exhibited an oncogenic function in OS cells, suggesting that inhibition of Skp2 may be a novel approach for the treatment of OS.

Indexed as

Cell MovementApoptosisCell CycleCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessOsteosarcomaS-Phase Kinase-Associated ProteinsS-Phase Kinase-Associated ProteinsApoptosiscell growthcell proliferationinvasionmigrationosteosarcomaSkp2

Identifiers

PMID28771075
PMCPMC5584850
OpenAlexW2743822624

What OpenQuestion holds

Textmetadata
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.