Evidence map›Paper›PMID 29537266›Full record

ArticleMolecular pharmaceutics2018

DNA Thioaptamer with Homing Specificity to Lymphoma Bone Marrow Involvement.

Junhua Mai, Xin Li, Guodong Zhang, Yi Huang, Rong Xu, Qi Shen, Ganesh L Lokesh, Varatharasa Thiviyanathan, Lingxiao Chen, Haoran Liu and 6 more

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2018. 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 26% 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, 16 citations in OpenAlex.

  1. Review
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  4. Article
  5. Article
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  9. Article
  10. Recent Advances in Aptamer Discovery and Applications.Molecules (Basel, Switzerland) · 2019
    Review
  11. 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

16 authors at 4 institutions in 2 countries.

Junhua MaiDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.ORCID 0000-0001-8374-4352
Xin LiInstitute of Molecular Medicine and the Department of Nanomedicine and Biomedical Engineering, McGovern Medical School , The University of Texas Health Science Center at Houston , 1825 Hermann Pressler , Houston 77030 , United States.
Guodong ZhangDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Yi HuangDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Rong XuDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Qi ShenDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Ganesh L LokeshInstitute of Molecular Medicine and the Department of Nanomedicine and Biomedical Engineering, McGovern Medical School , The University of Texas Health Science Center at Houston , 1825 Hermann Pressler , Houston 77030 , United States.
Varatharasa ThiviyanathanInstitute of Molecular Medicine and the Department of Nanomedicine and Biomedical Engineering, McGovern Medical School , The University of Texas Health Science Center at Houston , 1825 Hermann Pressler , Houston 77030 , United States.
Lingxiao ChenDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Haoran LiuDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Youli ZuDepartment of Pathology and Genomic Medicine , Houston Methodist Hospital , Houston , Texas 77030 , United States.
Xiaojing Ma
David E VolkInstitute of Molecular Medicine and the Department of Nanomedicine and Biomedical Engineering, McGovern Medical School , The University of Texas Health Science Center at Houston , 1825 Hermann Pressler , Houston 77030 , United States.
David G GorensteinInstitute of Molecular Medicine and the Department of Nanomedicine and Biomedical Engineering, McGovern Medical School , The University of Texas Health Science Center at Houston , 1825 Hermann Pressler , Houston 77030 , United States.
Mauro FerrariDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Haifa ShenDepartment of Nanomedicine , Houston Methodist Research Institute , Houston , Texas 77030 , United States.
Houston Methodist · USThe University of Texas Health Science Center at Houston · USCornell University · USMethodist Hospital · US

Funding

Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2009 to 2014
$10.8M
Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHANG, JENNY C-N · 2016 to 2020
$9.3M
Tumor vasculature-targeted nanotherapeutics for DNA damage responseR01CA193880 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI SHEN, HAIFA · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA193880NCI NIH HHS U54 CA143837NCI NIH HHS U54 CA151668NCI NIH HHS U54 CA210181
6 · The paper itself

Abstract

Selective drug accumulation in the malignant tissue is a prerequisite for effective cancer treatment. However, most drug molecules and their formulated particles are blocked en route to the destiny tissue due to the existence of multiple biological and physical barriers including the tumor microvessel endothelium. Since the endothelial cells on the surface of the microvessel wall can be modulated by inflammatory cytokines and chemokines secreted by the tumor or stromal cells, an effective drug delivery approach is to enhance interaction between the drug particles and the unique spectrum of surface proteins on the tumor endothelium. In this study, we performed in vivo screening for thioaptamers that bind to the bone marrow endothelium with specificity in a murine model of lymphoma with bone marrow involvement (BMI). The R1 thioaptamer was isolated based on its high homing potency to bones with BMI, and 40-60% less efficiency in accumulation to healthy bones. In cell culture, R1 binds to human umbilical vein endothelial cells (HUVEC) with a high affinity ( K

Indexed as

AnimalsAptamers, NucleotideBone MarrowBone Marrow CellsCell LineCell Line, TumorDNADoxorubicinDrug Delivery SystemsEndothelial CellsEndothelium, VascularFemaleHumansHuman Umbilical Vein Endothelial CellsLymphomaMiceAptamers, NucleotideDNADoxorubicinliposomal doxorubicinPolyethylene Glycolsbonein vivo SELEXlymphomathioaptamer

Identifiers

PMID29537266
PMCPMC6311132
OpenAlexW2789462894

What OpenQuestion holds

Textmetadata
LicenceTDM
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.