Evidence map›Paper›PMID 30320379›Full record

ArticleInternational journal of molecular medicine2018

SOSTDC1 inhibits bone metastasis in non-small cell lung cancer and may serve as a clinical therapeutic target.

Guanghui Chen, Haiyi Gong, Ting Wang, Jian Wang, Zhitao Han, Guangjian Bai, Shuai Han, Xinghai Yang, Wang Zhou, Tielong Liu and 1 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 21 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

11 authors at 3 institutions in 1 country.

Guanghui ChenOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Haiyi GongOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Ting WangOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Jian WangDepartment of Orthopedics, Pudong New District People's Hospital, Shanghai 201200, P.R. China.
Zhitao HanOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Guangjian BaiDepartment of Orthopedics, Affiliated Hospital of Taishan Medical University, Taishan Medical University, Tai'an, Shandong 271016, P.R. China.
Shuai HanOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Xinghai YangOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Wang ZhouOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Tielong LiuOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Jianru XiaoOrthopedic Oncology Center, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.
Second Military Medical University · CNAffiliated Hospital of Taishan Medical University · CNPudong New Area People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone metastasis occurs in ~40% patients with non‑small cell lung cancer (NSCLC), resulting in serious morbidity and mortality. Sclerostin domain‑containing protein 1 (SOSTDC1) has been demonstrated to be associated with the development and progression of multiple types of cancer. However, the role of SOSTDC1 in NSCLC bone metastasis remains unclear. In the present study, it was identified that SOSTDC1 was downregulated in NSCLC bone metastatic lesions compared with that in primary tumors, and low SOSTDC1 expression predicted poor prognosis for patients with NSCLC. Functionally, SOSTDC1 overexpression suppressed NSCLC cell proliferation, migration, invasion and cancer cell‑induced osteoclastogenesis, while SOSTDC1 knockdown produced the opposite effect. In addition, a number of potential downstream target genes of SOSTDC1, which were demonstrated to be associated with tumor progression and bone metastasis, were identified in NSCLC cells by RNA deep sequencing and RT‑qPCR assays. The results from the present study may provide useful insight for an improved understanding of the pathogenesis of NSCLC bone metastasis, and suggest that SOSTDC1 may be a potential prognostic biomarker and therapeutic target for NSCLC bone metastasis.

Indexed as

Molecular Targeted TherapyAdaptor Proteins, Signal TransducingAnimalsBone NeoplasmsCarcinoma, Non-Small-Cell LungCell DifferentiationCell Line, TumorCell MovementCell ProliferationDown-RegulationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsLung NeoplasmsAdaptor Proteins, Signal TransducingIntracellular Signaling Peptides and ProteinsProteinsSOSTDC1 protein, human

Identifiers

PMID30320379
PMCPMC6202094
OpenAlexW2896357401

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.