Evidence map›Paper›PMID 35433114›Full record

ArticleOncoimmunology2022

Cell-directed aptamer therapeutic targeting for cancers including those within the central nervous system.

Jun Wei, Renduo Song, Aria Sabbagh, Anantha Marisetty, Neal Shukla, Dexing Fang, Hinda Najem, Martina Ott, James Long, Lijie Zhai and 5 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

  1. Aptamer targeting proprotein convertase subtilisin/kexin type 9:Research in pharmaceutical sciences · 2026
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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

15 authors at 2 institutions in 1 country.

Jun WeiDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Renduo SongDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Aria SabbaghDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Anantha MarisettyDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Neal ShuklaDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Dexing FangDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Hinda NajemDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Martina OttDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
James LongDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lijie ZhaiDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Maciej S LesniakDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Charles David JamesDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Leonidas PlataniasRobert H. Lurie Comprehensive Cancer Center and Division of Hematology-Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Michael CurranDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Amy B HeimbergerDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID 0000-0002-9970-8695
The University of Texas MD Anderson Cancer Center · USNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteopontin (OPN) is produced by tumor cells as well as by myeloid cells and is enriched in the tumor microenvironment (TME) of many cancers. Given the roles of OPN in tumor progression and immune suppression, we hypothesized that targeting OPN with aptamers that have high affinity and specificity could be a promising therapeutic strategy. Bi-specific aptamers targeting ligands for cellular internalization were conjugated to siRNAs to suppress OPN were created, and therapeutic leads were selected based on target engagement and

Indexed as

Aptamers, NucleotideBreast NeoplasmsGliomaCentral Nervous SystemFemaleHumansRNA, Small InterferingTumor MicroenvironmentAptamers, NucleotideRNA, Small Interferingaptamersbrain cancerbreast cancerCpG ODNlung cancernucleolinOsteopontinsiRNA

Identifiers

PMID35433114
PMCPMC9009928
OpenAlexW4223934660

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.