Evidence map›Paper›PMID 27572315›Full record

ArticleOncotarget2016

Identification of SHCBP1 as a novel downstream target gene of SS18-SSX1 and its functional analysis in progression of synovial sarcoma.

Changliang Peng, Hui Zhao, Wei Chen, Yan Song, Xiaoying Wang, Ji Li, Yong Qiao, Dongjin Wu, Shengzhong Ma, Xiuwen Wang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. SHCBP1 promotes cisplatin resistance of ovarian cancer through AKT/mTOR/Autophagy pathway.Apoptosis : an international journal on programmed cell death · 2025
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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 2 institutions in 1 country.

Changliang PengDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Hui ZhaoDepartment of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Wei ChenBeijing Institute of Pharmacology and Toxicology, Beijing, China.
Yan SongNephrology Research Institute, Shandong University Second Hospital, Jinan, China.
Xiaoying WangDepartment of Pathology, Shandong University Second Hospital, Jinan, China.
Ji LiDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Yong QiaoDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Dongjin WuDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Shengzhong MaDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Xiuwen WangDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Chunzheng GaoDepartment of Orthopaedics, Shandong University Second Hospital, Jinan, China.
Second Hospital of Shandong University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SS18-SSX1 fusion gene has been shown to play important roles in the development of synovial sarcoma (SS), but the underlying molecular mechanisms and its downstream target genes are still not clear. Here SHC SH2-domain binding protein 1 (SHCBP1) was identified and validated to be a novel downstream target gene of SS18-SSX1 by using microarray assay, quantitative real-time (qPCR) and western blot. Expression of SHCBP1 was firstly confirmed in SS cell line and SS tissues. The effects of SHCBP1 overexpression or knockdown on SS cell proliferation and tumorigenicity were then studied by cell proliferation, DNA replication, colony formation, flow cytometric assays, and its in vivo tumorigenesis was determined in the nude mice. Meanwhile, the related signaling pathways of SHCBP1 were also examined in SS cells. The results indicated that SHCBP1 was significantly increased in SS cells and SS tissues compared with adjacent noncancerous tissues. The expression of SHCBP1 was demonstrated to be positively correlated with the SS18-SSX1 level. Overexpression and ablation of SHCBP1 promoted and inhibited, respectively, the proliferation and tumorigenicity of SS cells in vitro. SHCBP1 knockdown also significantly inhibited SS cell growth in nude mice, and lowered the MAPK/ERK and PI3K/AKT/mTOR signaling pathways and cyclin D1 expression. Our findings disclose that SHCBP1 is a novel downstream target gene of SS18-SSX1, and demonstrate that the oncogene SS18-SSX1 promotes tumorigenesis by increasing the expression of SHCBP1, which normally acts as a tumor promoting factor.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell CycleCell Line, TumorCell ProliferationDisease ProgressionGene Expression ProfilingHumansMice, Inbred BALB CMice, NudeOncogene Proteins, FusionRNA InterferenceRNAi TherapeuticsSarcoma, SynovialShc Signaling Adaptor ProteinsSignal TransductionOncogene Proteins, FusionSHCBP1 protein, humanShc Signaling Adaptor ProteinsSS18-SSX1 fusion proteinapoptosisproliferationSHCBP1SS18-SSX1synovial sarcoma

Identifiers

PMID27572315
PMCPMC5341840
OpenAlexW2512225853

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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.