Evidence map›Paper›PMID 28572530›Full record

ArticleOncotarget2017

Assessment of GSK1904529A as a promising anti-osteosarcoma agent.

Hao-Dong Fei, Qi Yuan, Li Mao, Feng-Li Chen, Zhao-Hui Cui, Sha Tao, Feng Ji

Abstract read
In one paragraph

Article in Oncotarget, 2017. 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.

  1. Metabolic Strategies for Inhibiting Cancer Development.Advances in nutrition (Bethesda, Md.) · 2021
    Review
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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

7 authors.

Hao-Dong FeiDepartment of Orthopedics, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Qi YuanDepartment of Endocrinology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Li MaoDepartment of Endocrinology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Feng-Li ChenClinical Laboratory, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Zhao-Hui CuiDepartment of Endocrinology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Sha TaoDepartment of Endocrinology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Feng JiDepartment of Orthopedics, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The insulin growth factor-I receptor (IGF1R) signaling is a key mechanism for osteosarcoma (OS) cell proliferation. GSK1904529A is a novel small molecule IGF1R kinase inhibitor. Its activity against OS cells was tested. In both established OS cell lines (Saos-2 and MG-63) and primary human OS cells, treatment with GSK1904529A (at nM concentrations) significantly inhibited cell proliferation. At the molecular level, GSK1904529A almost completely blocked IGF1R activation in OS cells, and inhibited downstream AKT-ERK activation. IGF1R silence by targeted shRNA also inhibited AKT-ERK activation and Saos-2 cell proliferation. Significantly, GSK1904529A was unable to further inhibit proliferation of IGF1R-silenced Saos-2 cells. In vivo, GSK1904529A administration orally inhibited Saos-2 tumor growth in nude mice. Together, these results suggest that targeting IGF1R by GSK1904529A inhibits OS cell growth in vitro and in vivo.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCaspase 3Cell CycleCell Line, TumorCell ProliferationDisease Models, AnimalGene Knockdown TechniquesHumansImidazolesMaleMiceOsteosarcomaPyridinesReceptor, IGF Type 1Antineoplastic AgentsCaspase 3GSK1904529AImidazolesPyridinesReceptor, IGF Type 1GSK1904529AIGF1Rosteosarcomaproliferation

Identifiers

PMID28572530
PMCPMC5564795

What OpenQuestion holds

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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.