Evidence map›Paper›PMID 29528777›Full record

ArticleTechnology in cancer research & treatment2018

ING5 is a Potential Target for Osteosarcoma Therapy.

Xing Zhang, Zhong-Hua Xu, Hua Xie, Ya-Wen Sun, Jun Liu, Yin-Bi Zhao

Abstract read
In one paragraph

Article in Technology in cancer research & treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. The roles of ING5 in cancer: A tumor suppressor.Frontiers in cell and developmental biology · 2022
    Review
  4. Review
  5. 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

6 authors.

Xing Zhang1 Department of Orthopedics, Jintan Hospital Affiliated to Jiangsu University, Jintan, Jiangsu, People's Republic of China.
Zhong-Hua Xu1 Department of Orthopedics, Jintan Hospital Affiliated to Jiangsu University, Jintan, Jiangsu, People's Republic of China.
Hua Xie1 Department of Orthopedics, Jintan Hospital Affiliated to Jiangsu University, Jintan, Jiangsu, People's Republic of China.
Ya-Wen Sun1 Department of Orthopedics, Jintan Hospital Affiliated to Jiangsu University, Jintan, Jiangsu, People's Republic of China.
Jun Liu1 Department of Orthopedics, Jintan Hospital Affiliated to Jiangsu University, Jintan, Jiangsu, People's Republic of China.
Yin-Bi Zhao1 Department of Orthopedics, Jintan Hospital Affiliated to Jiangsu University, Jintan, Jiangsu, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is one of the most common primary malignant bone tumors. The inhibitor of growth family of protein 5 has been identified as a tumor suppressor in many cancers. In this study, we confirmed the downregulation of the both inhibitor of growth family of protein 5 and messenger RNA levels in cancer tissues using Western blot and real-time polymerase chain reaction. In order to find the antitumor roles of inhibitor of growth family of protein 5, osteosarcoma cells, HOS, and MG63 were transfected with the plasmid pCDNA-3.1-inhibitor of growth family of protein 5. Overexpression of Inhibitor of growth family of protein 5 could induce apoptosis and inhibit cell proliferation in osteosarcoma cells. Furthermore, Western blot analysis showed that p-Smad2, p-Smad3, and Smad4 were increased in inhibitor of growth family of protein 5-expressing osteosarcoma cells. Our results indicated that overexpression of inhibitor of growth family of protein 5 in osteosarcoma cells induces apoptosis by activating the Smad pathway, thus proposing a promising role for inhibitor of growth family of protein 5 in treatment of patients with osteosarcoma.

Indexed as

ApoptosisBiomarkers, TumorBone NeoplasmsCell Line, TumorCell ProliferationFemaleHumansMaleOsteosarcomaSmad ProteinsTranscription FactorsTumor Suppressor ProteinsBiomarkers, TumorING5 protein, humanSmad ProteinsTranscription FactorsTumor Suppressor ProteinsapoptosisING5osteosarcomasurvival ratethe Smad pathway

Identifiers

PMID29528777
PMCPMC5851100

What OpenQuestion holds

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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.