Evidence map›Paper›PMID 24900417›Full record

ArticleACS medicinal chemistry letters2012

Development of Synthetic Aminopeptidase N/CD13 Inhibitors to Overcome Cancer Metastasis and Angiogenesis.

Li Su, Jiangying Cao, Yuping Jia, Xiaonan Zhang, Hao Fang, Wenfang Xu

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. BioMed research international · 2020
    Article
  5. Article
  6. Article
  7. Evaluation ofTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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

6 authors.

Li SuDepartment of Medicinal Chemistry, School of Pharmacy, Shandong University , 250012 Ji'nan, Shandong, PR China.
Jiangying CaoDepartment of Medicinal Chemistry, School of Pharmacy, Shandong University , 250012 Ji'nan, Shandong, PR China.
Yuping JiaDepartment of Medicinal Chemistry, School of Pharmacy, Shandong University , 250012 Ji'nan, Shandong, PR China.
Xiaonan ZhangDepartment of Medicinal Chemistry, School of Pharmacy, Shandong University , 250012 Ji'nan, Shandong, PR China.
Hao FangDepartment of Medicinal Chemistry, School of Pharmacy, Shandong University , 250012 Ji'nan, Shandong, PR China.
Wenfang XuDepartment of Medicinal Chemistry, School of Pharmacy, Shandong University , 250012 Ji'nan, Shandong, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer metastasis is a major barrier to its treatment and an important cause of patient death. Antimetastatic agents hold promise for patients with advanced metastatic tumors. Aminopeptidase N/CD13 (APN) is being pursued by many as an important target against cancer metastasis and angiogenesis, but there are few reports on the in vivo evaluation of synthetic APN inhibitors. Herein, a series of compounds targeting APN were synthesized and evaluated for their antimetastasis and antiangiogenesis potency both in vitro and in vivo. Excitingly, compounds 4m, 4t, and 4cc, with the most potent APN inhibitory activities, displayed significant antimetastasis and antiangiogenesis effects in vitro and in vivo, suggesting that those synthetic APN inhibitors have the potential to overcome cancer metastasis and angiogenesis.

Indexed as

angiogenesisanticancerAPN/CD13inhibitorsmetastasis

Identifiers

PMID24900417
PMCPMC4025871

What OpenQuestion holds

Textmetadata
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.