Evidence map›Paper›PMID 28053291›Full record

ArticleOncotarget2016

SPARC expression in gastric cancer predicts poor prognosis: Results from a clinical cohort, pooled analysis and GSEA assay.

Zhi Li, Ao-Di Li, Lu Xu, De-Wei Bai, Ke-Zuo Hou, Hua-Chuan Zheng, Xiu-Juan Qu, Yun-Peng Liu

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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 23 citations in OpenAlex.

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  8. Genome-Scale Analysis Identified NID2, SPARC, and MFAP2 as Prognosis Markers of Overall Survival in Gastric Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2021
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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

8 authors at 3 institutions in 1 country.

Zhi LiDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
Ao-Di LiDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
Lu XuDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
De-Wei BaiDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
Ke-Zuo HouDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
Hua-Chuan ZhengLife Science Institute of Jinzhou Medical University, Jinzhou, Liaoning Province, China.
Xiu-Juan QuDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
Yun-Peng LiuDepartment of Medical Oncology, The First Hospital, China Medical University, Shenyang, Liaoning Province, China.
First Hospital of China Medical University · CNChina Medical University · CNJinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognostic role of Secreted Protein Acidic and Rich in Cysteine (SPARC) in gastric cancer (GC) remains controversial. We investigated the clinical significance, the survival relevance, and potential function of SPARC in GC with resected samples, online gene set GSE62254, and cell line SGC7901.

resultsHigh immunostaining of SPARC significantly correlated with tumor differentiation (P = 0.004), and independently predicted shorter overall survival (OS) (HR = 1.446, P = 0.022), based on the current IHC evaluation. The accuracy of the results was further validated with 1000 times bootstrapping and the time-dependent receiver-operating characteristics (ROC) curves. The meta-analysis (pooled HR = 1.60, 95% CI: 1.01-2.53) confirmed SPARC as the predictor for reduced OS in GC. Moreover, the association between enhanced SPARC expression and Adriamycin (Adr) sensitivity was revealed by GSEA, and then confirmed by comparative cellular experiments, such as the protein level analysis of SGC7901and SGC7901/Adr cell line. MATERIALS AND

methodsImmunohistochemistry (IHC) method was used to detect SPARC expression in 137 GC cases. Meta-analysis was performed based on 5 studies published in English on PubMed up to March 2016. GSEA was performed using online data set GSE62254 and GC-related functional gene sets derived from molecular signatures database (MSigDB). Western Blot was carried out to compare protein-level differences between gastric carcinoma SGC7901 cell line and Adr resistant SGC7901/Adr cell line. MTT assay was done to confirm the induction of SPARC on Adr sensitivity.

conclusionsIncreased SPARC expression in GC led to a worse clinical outcome of patients and might induce Adr sensitivity of GC cells.

Indexed as

AdultAgedCell Line, TumorCohort StudiesDoxorubicinFemaleHumansMaleMiddle AgedOsteonectinPrognosisStomach NeoplasmsDoxorubicinOsteonectinSPARC protein, humangastric cancerGSEAimmunohistochemistryprognosisSPARC

Identifiers

PMID28053291
PMCPMC5342547
OpenAlexW2521490417

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.