Evidence map›Paper›PMID 31726389›Full record

ArticleMolecular therapy. Nucleic acids2019

A Novel Aptamer LL4A Specifically Targets Vemurafenib-Resistant Melanoma through Binding to the CD63 Protein.

Hui Li, Juan Liu, Xiaojuan Xiao, Shuming Sun, Hui Zhang, Yibin Zhang, Weihua Zhou, Bin Zhang, Mridul Roy, Hong Liu and 4 more

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. [Advances in exosome-targeting aptamer-screening techniques].Se pu = Chinese journal of chromatography · 2025
    Review
  4. Article
  5. Aptamer-based Advances in Skin Cancer Research.Current medicinal chemistry · 2023
    Review
  6. Review
  7. Article
  8. Elucidation of CKAP4-remodeled cell mechanics in driving metastasis of bladder cancer through aptamer-based target discovery.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Aptasensors for Cancerous Exosome Detection.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  10. Review
  11. Review
  12. Aptamers: Cutting edge of cancer therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    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

14 authors.

Hui LiMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China.
Juan LiuMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China.
Xiaojuan XiaoMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China.
Shuming SunMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China.
Hui ZhangMolecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, China.
Yibin ZhangMolecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, China.
Weihua ZhouMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China; Department of Obstetrics and Gynecology, People's Hospital of Xiangxi Tujia and Miao Autonomous Prefecture, Hunan, Jishou 410006, China.
Bin ZhangDepartment of Histology and Embryology, Xiangya School of Medicine, Central South University, Changsha 410013, China.
Mridul RoyMolecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, China.
Hong LiuThe First Xiangya Hospital, Central South University, Changsha 410078, China.
Mao YeMolecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, China.
Zi WangMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China; The First Xiangya Hospital, Central South University, Changsha 410078, China. Electronic address: zhongnanwangzi@126.com.
Feng Liu-SmithMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China; Department of Epidemiology, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA. Electronic address: liufe@uci.edu.
Jing LiuMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha 410078, China. Electronic address: liujing2@sklmg.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is a highly aggressive tumor with a poor prognosis, and half of all melanoma patients harbor BRAF mutations. A BRAF inhibitor, vemurafenib (PLX4032), has been approved by the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) to treat advanced melanoma patients with BRAF

Indexed as

aptamerCD63LL4Amelanomavemurafenib-resistant

Identifiers

PMID31726389
PMCPMC6859286

What OpenQuestion holds

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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.