Evidence map›Paper›PMID 26375249›Full record

ArticleOncotarget2015

RD3 loss dictates high-risk aggressive neuroblastoma and poor clinical outcomes.

Faizan H Khan, Vijayabaskar Pandian, Satish Kumar Ramraj, Sheeja Aravindan, Mohan Natarajan, Seifollah Azadi, Terence S Herman, Natarajan Aravindan

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 17 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

8 authors at 4 institutions in 2 countries.

Faizan H KhanDepartment of Radiation Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Vijayabaskar PandianDepartment of Radiation Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Satish Kumar RamrajDepartment of Radiation Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Sheeja AravindanStephenson Cancer Center, Oklahoma City, OK, USA.
Mohan NatarajanDepartment of Pathology, University of Texas Health Sciences Center at San Antonio, San Antonio, TX, USA.
Seifollah AzadiDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Terence S HermanDepartment of Radiation Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Natarajan AravindanDepartment of Radiation Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
University of Oklahoma Health Sciences Center · USOU Health Stephenson Cancer CenterThe University of Texas Health Science Center at San Antonio · USTranslational Research in Oncology · FR

Funding

TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
NIGMS NIH HHS 1P20GM103639-01NIGMS NIH HHS P20 GM103639
6 · The paper itself

Abstract

Clinical outcomes for high-risk neuroblastoma patients remains poor, with only 40-50% 5-Year overall survival (OS) and <10% long-term survival. The ongoing acquisition of genetic/molecular rearrangements in undifferentiated neural crest cells may endorse neuroblastoma progression. This study recognized the loss of Retinal Degeneration protein 3, RD3 in aggressive neuroblastoma, and identified its influence in better clinical outcomes and defined its novel metastasis suppressor function. The results showed ubiquitous expression of RD3 in healthy tissues, complete-loss and significant TNM-stage association of RD3 in clinical samples. RD3-loss was intrinsically associated with reduced OS, abridged relapse-free survival, aggressive stage etc., in neuroblastoma patient cohorts. RD3 was transcriptionally and translationally regulated in metastatic site-derived aggressive (MSDAC) cells (regardless of CSC status) ex vivo and in tumor manifolds from metastatic sites in reproducible aggressive disease models in vivo. Re-expressing RD3 in MSDACs reverted their metastatic potential both in vitro and in vivo. Conversely muting RD3 in neuroblastoma cells not only heightened invasion/migration but also dictated aggressive disease with metastasis. These results demonstrate the loss of RD3 in high-risk neuroblastoma, its novel, thus-far unrecognized metastasis suppressor function and further imply that RD3-loss may directly relate to tumor aggressiveness and poor clinical outcomes.

Indexed as

AnimalsCell Line, TumorDisease ProgressionEye ProteinsHeterograftsHumansMiceNeuroblastomaSurvival AnalysisTissue Array AnalysisTreatment OutcomeEye ProteinsRD3 protein, humanhigh-risk aggressive neuroblastomametastasisneuroblastomaRD3tumor suppressor

Identifiers

PMID26375249
PMCPMC4742193
OpenAlexW1897671347

What OpenQuestion holds

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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 OpenQuestion graph.