Evidence map›Paper›PMID 29290950›Full record

ArticleOncotarget2017

Human fibulin-3 protein variant expresses anti-cancer effects in the malignant glioma extracellular compartment in intracranial xenograft models.

Yanyan Li, Yuan Hu, Chuanjin Liu, Qingyue Wang, Xiaoxiao Han, Yong Han, Xue-Shun Xie, Xiong-Hui Chen, Xiang Li, Eric R Siegel and 4 more

Open access · diamondAbstract 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
0.8field-weighted citation impact, top 28% 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, 8 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

14 authors at 5 institutions in 4 countries.

Yanyan LiNeurosurgery & Brain and Nerve Research Laboratory.
Yuan HuNeurosurgery & Brain and Nerve Research Laboratory.
Chuanjin LiuNeurosurgery & Brain and Nerve Research Laboratory.
Qingyue WangNeurosurgery & Brain and Nerve Research Laboratory.
Xiaoxiao HanNeurosurgery & Brain and Nerve Research Laboratory.
Yong HanNeurosurgery & Brain and Nerve Research Laboratory.
Xue-Shun XieNeurosurgery & Brain and Nerve Research Laboratory.
Xiong-Hui ChenDepartment of Emergency Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Xiang LiNeuroepigenetic Reseach Lab, Queensland Brain Institute, The University of Queensland, St Lucia, QLD, Australia.
Eric R SiegelDepartment of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Kambiz AfrasiabiBrain Tumor Research Laboratory, Department of Surgery, University of California Irvine, Irvine, CA, USA.
Mark E LinskeyBrain Tumor Research Laboratory, Department of Surgery, University of California Irvine, Irvine, CA, USA.
You-Xin ZhouNeurosurgery & Brain and Nerve Research Laboratory.
Yi-Hong ZhouNeurosurgery & Brain and Nerve Research Laboratory.
Nerve Centre · GBUniversity of California, Irvine · USSoochow University · CNUniversity of Arkansas for Medical Sciences · USUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDecades of cytotoxic and more recently immunotherapy treatments for malignant glioma have had limited success due to dynamic intra-tumoral heterogeneity. The dynamic interplay of cancer cell subpopulations has been found to be under the control of proteins in the cancer microenvironment. EGF-containing fibulin-like extracellular matrix protein (EFEMP1) (also fibulin-3) has the multiple functions of suppressing cancer growth and angiogenesis, while promoting cancer cell invasion. EFEMP1-derived tumor suppressor protein (ETSP) retains EFEMP1's anti-growth and anti-angiogenic functions while actually inhibiting cancer cell invasion.

methodsIn this study, we examined the therapeutic effect on glioblastoma multiforme (GBM) of an

resultsZR30 showed the same effects as ETSP in blocking EGFR/NOTCH/AKT signaling pathways, when applied to cultures of multiple GBM cell lines and primary cultures. ZR30's inhibition of MMP2 activation was shown not only for GBM cells, but also for other types of cancer cells having overexpression of MMP2. A significant improvement in survival of mice with orthotopic human GBM xenografts was observed after a single, intra-tumoral injection of ZR30. Using a model mimicking the intra-tumoral heterogeneity of GBM with cell subpopulations carrying different invasive and proliferative phenotypes, we demonstrated an equal and simultaneous tumor suppressive effect of ZR30 on both tumor cell subpopulations, with suppression of

conclusionOverall, the data support a complementary pleiotrophic therapeutic effect of ZR30 acting in the extracellular compartment of GBM.

Indexed as

EGFR/NOTHC signalingGBMMMP2protein therapeuticstumor heterogeneity in vivo model

Identifiers

PMID29290950
PMCPMC5739735
OpenAlexW2767626176

What OpenQuestion holds

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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.