Evidence map›Paper›PMID 29303005›Full record

ArticleDrug delivery2018

Bone-targeted methotrexate-alendronate conjugate inhibits osteoclastogenesis in vitro and prevents bone loss and inflammation of collagen-induced arthritis in vivo.

Zi'ang Xie, Guanxiong Liu, Pan Tang, Xuewu Sun, Shuai Chen, An Qin, Peizhi Zhu, Jianfeng Zhang, Shunwu Fan

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Engineering small-molecule and protein drugs for targeting bone tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. FITC-Labeled Alendronate as an In Vivo Bone pH Sensor.BioMed research international · 2020
    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

9 authors at 4 institutions in 1 country.

Zi'ang Xiea Department of Orthopaedics , Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
Guanxiong Liuc School of Chemistry and Chemical Engineering , Yangzhou University , Jiangsu , China.
Pan Tanga Department of Orthopaedics , Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
Xuewu Suna Department of Orthopaedics , Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
Shuai Chena Department of Orthopaedics , Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
An Qind Department of Orthopaedics, Shanghai Key Laboratory of Orthopaedic Implant , Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine , Shanghai , PR China.
Peizhi Zhuc School of Chemistry and Chemical Engineering , Yangzhou University , Jiangsu , China.
Jianfeng Zhanga Department of Orthopaedics , Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
Shunwu Fana Department of Orthopaedics , Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University , Hangzhou , China.
Sir Run Run Shaw Hospital · CNYangzhou University · CNShanghai Ninth People's Hospital · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA), a disease that causes joint destruction and bone erosion, is related to osteoclast activity. RA is generally treated with methotrexate (MTX). In this study, a MTX-Alendronate (ALN) conjugate was synthesized and characterized. The conjugate dramatically inhibited osteoclast formation and bone resorption compared with MTX and ALN used alone or in combination. Due to the characteristics of ALN, the MTX-ALN conjugate can adhere to the exposed bone surface and enhance drug accumulation in the pathological region for targeted therapy against osteoclastogenesis. Additionally, MTX was rapidly released in the presence of lysozyme under mildly acidic conditions, similar to inflammatory tissue and osteoclast-surviving conditions, which contributes to inflammatory inhibition; this was confirmed by the presence of pro-inflammatory cytokines. Our study highlights the use of the MTX-ALN conjugate as a potential therapeutic approach for RA by targeting osteoclastogenesis.

Indexed as

AlendronateAnimalsArthritis, ExperimentalArthritis, RheumatoidBone and BonesBone ResorptionCollagenCytokinesDrug Therapy, CombinationFemaleInflammationMaleMethotrexateMiceMice, Inbred C57BLMuramidaseAlendronateCollagenCytokinesMethotrexateMuramidasealendronatebone targetingmethotrexateRheumatoid arthritistherapeutic

Identifiers

PMID29303005
PMCPMC6058523
OpenAlexW2782440322

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.