Evidence map›Paper›PMID 34363435›Full record

ArticleJournal of cellular and molecular medicine2021

Hematopoietic cell kinase enhances osteosarcoma development via the MEK/ERK pathway.

Weibo Liu, Teng Li, Wenhao Hu, Quanbo Ji, Fanqi Hu, Qi Wang, Xiaoqing Yang, Dengbin Qi, Hui Chen, Xuesong Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. 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
0.7field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Weibo LiuDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Teng LiDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Wenhao HuDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Quanbo JiDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Fanqi HuDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Qi WangDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Xiaoqing YangDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Dengbin QiDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.
Hui ChenCollege of Life Sciences, East China Normal University, Shanghai, China.
Xuesong ZhangDepartment of Orthopaedics, The Fourth Medical Centre, Chinese PLA General Hospital, Beijing, China.ORCID 0000-0002-1934-5717
Chinese PLA General Hospital · CNEast China Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is a sarcoma with high rates of pulmonary metastases and mortality. The mechanisms underlying tumour generation and development in OS are not well-understood. Haematopoietic cell kinase (HCK), a vital member of the Src family of kinase proteins, plays crucial roles in cancer progression and may act as an anticancer target; however, the mechanism by which HCK enhances OS development remains unexplored. Therefore, we investigated the role of HCK in OS development in vitro and in vivo. Downregulation of HCK attenuated OS cell proliferation, migration and invasion and increased OS cell apoptosis, whereas overexpression of HCK enhanced these processes. Mechanistically, HCK expression enhanced OS tumorigenesis via the mitogen-activated protein kinase (MEK)/extracellular signal-regulated kinase (ERK) pathway; HCK upregulation increased the phosphorylation of MEK and ERK and promoted epithelial-mesenchymal transition, with a reduction in E-cadherin in vitro. Furthermore, HCK downregulation decreased the tumour volume and weight in mice transplanted with OS cells. In conclusion, HCK plays a crucial role in OS tumorigenesis, progression and metastasis via the MEK/ERK pathway, suggesting that HCK is a potential target for developing treatments for OS.

Indexed as

AnimalsBone NeoplasmsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMAP Kinase Kinase KinasesMiceMice, Inbred BALB COsteosarcomaProto-Oncogene Proteins c-hckHck protein, mouseMAP Kinase Kinase KinasesProto-Oncogene Proteins c-hckcell migrationERK signalling pathwayHCKMEKosteosarcomatumorigenesis

Identifiers

PMID34363435
PMCPMC8435456
OpenAlexW3192778309

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.