Evidence map›Paper›PMID 24603483›Full record

ArticlePloS one2014

Cell-SELEX aptamer for highly specific radionuclide molecular imaging of glioblastoma in vivo.

Xidong Wu, Huiyu Liang, Yan Tan, Chao Yuan, Shuji Li, Xiaowen Li, Guiping Li, Yusheng Shi, Xingmei Zhang

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. In Vivo Evaluation ofPharmaceutics · 2024
    Article
  12. Review
  13. Review
  14. Radiochemical Synthesis of 4-[Molecules (Basel, Switzerland) · 2022
    Article
  15. Therapeutic Potential of Aptamer-Protein Interactions.ACS pharmacology & translational science · 2022
    Review
  16. Advances in aptamer-based nuclear imaging.European journal of nuclear medicine and molecular imaging · 2022
    Review
  17. Aptamer Applications in Neuroscience.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  18. Article
  19. Review
  20. Review
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

9 authors.

Xidong WuDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Huiyu LiangDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Yan TanDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Chao YuanDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shuji LiDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Xiaowen LiDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Guiping LiDepartment of Nuclear Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yusheng ShiDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Xingmei ZhangDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most frequent and aggressive primary adult brain tumor with poor prognosis. Epidermal growth factor receptor variant III (EGFRvIII) is the most common and highly oncogenic EGFR mutant in GBM. With the aim to generate specific molecular probes able to target EGFRvIII with high affinity, we selected four DNA aptamers (U2, U8, U19 and U31) specifically bound to U87-EGFRvIII cells that over expressed EGFRvIII with Kd values in the nanomole range by a cell-based systematic evolution of ligands by exponential enrichment (cell-SELEX) process. U87MG cells were introduced as control cells for counter selection. We further affirmed U2 and U8 identified EGFRvIII on the surface of target cells specifically. Then we radiolabeled U2 with 188Re to serve as a molecular imaging probe and observed 188Re -labeled U2 significantly targeted EGFRvIII over-expressing glioblastoma exnografts in mice. In conclusion, aptamers obtained from whole cell-SELEX strategy have great potential as molecular imaging probes that are probably beneficial to GBM diagnoses.

Indexed as

DNA ProbesRadiopharmaceuticalsAnimalsBase SequenceBrain NeoplasmsCell Line, TumorErbB ReceptorsGlioblastomaHumansMaleMice, Inbred BALB CMice, NudeNeoplasm TransplantationRadionuclide ImagingSELEX Aptamer TechniqueDNA Probesepidermal growth factor receptor VIIIErbB ReceptorsRadiopharmaceuticals

Identifiers

PMID24603483
PMCPMC3948368

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.