Evidence map›Paper›PMID 30323562›Full record

ArticleDrug design, development and therapy2018

Evaluation of methotrexate-conjugated gadolinium(III) for cancer diagnosis and treatment.

Dan Xu, Shu-Ting Lu, Yu-Shuang Li, Aju Baidya, Hao Mei, Yong He, Bo Wu

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

7 authors.

Dan XuDepartment of Nuclear Medicine, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, vincentheyong@163.com.
Shu-Ting LuDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, wubo5317@whu.edu.cn.
Yu-Shuang LiDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, wubo5317@whu.edu.cn.
Aju BaidyaDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, wubo5317@whu.edu.cn.
Hao MeiDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, wubo5317@whu.edu.cn.
Yong HeDepartment of Nuclear Medicine, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, vincentheyong@163.com.
Bo WuDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, PR China, wubo5317@whu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGliomas are one of the most common types of primary brain tumors. It is usually evaluated by gadolinium(III)-based contrast agents by magnetic resonance imaging (MRI) in the clinic. Methotrexate (MTX), as a type of folate analog that inhibits the enzyme dihydrofolate reductase, is widely used as a chemotherapeutic agent to treat gliomas in the experiment. PURPOSE: In this study, a novel theranostic agent MTX-DOTA-Gd (MTX-Gd) was synthesized, which integrates magnetic resonance imaging (MRI) with anticancer treatment.

methodsMTX-Gd was synthesized by connecting MTX and Gd through 1,4,7,10-tetraazacy-clododecane-1,4,7,10-tetraacetic acid (DOTA). The characterization of MTX-Gd was detected by ultraviolet (UV) and infrared spectroscopy (IR). To confirm the antitumor effect of MTX-Gd, the cytotoxicity of MTX-Gd was examined by the MTT assay. The contrast enhancement of the MTX-Gd was measured through MRI in vitro. Then, nude mice bearing C6 tumor xenografts were used to study in vivo imaging capabilities.

resultsThe ultraviolet-visible-near infrared radiation (UV-NIR) absorption curve indicated that MTX-Gd had a broad absorption in the region of 500-700 nm. The formation of MTX-Gd was confirmed from the characteristic bands of MTX-DOTA-Gd in the 1413 cm

conclusionA novel stable and unique theranostic agent (MTX-Gd) was successfully synthe-sized, and it has good stability, strong anticancer ability and excellent magnetic capacity. The methotrexate component of MTX-Gd, as a chemotherapeutic agent, played an important role in targeted therapies of cancer. The DOTA-Gd component of MTX-Gd performed as the MRI contrast agent. The superior MRI imaging performance and synergetic chemical antineoplastic ability of MTX-Gd was revealed, and it has great potential in the diagnosis and treatment of glioma and potentially other cancers, with prospects of clinical application in the near future.

Indexed as

AnimalsAntimetabolites, AntineoplasticBrain NeoplasmsCell ProliferationCell SurvivalContrast MediaDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleGadoliniumGliomaHumansMagnetic Resonance ImagingMethotrexateMiceMice, Inbred BALB CAntimetabolites, AntineoplasticContrast MediaGadoliniumMethotrexateOrganometallic Compoundsgadoliniumgliomamethotrexatetheranostics

Identifiers

PMID30323562
PMCPMC6181113

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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.