Evidence map›Paper›PMID 25294818›Full record

ArticleOncotarget2014

Glipizide, an antidiabetic drug, suppresses tumor growth and metastasis by inhibiting angiogenesis.

Cuiling Qi, Qin Zhou, Bin Li, Yang Yang, Liu Cao, Yuxiang Ye, Jiangchao Li, Yi Ding, Huiping Wang, Jintao Wang and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 52 citations in OpenAlex.

  1. Uncovering hypothesis-generating associations between prescription drugs and digestive cancer risk: a case-control drug-wide association study (DWAS).Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
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  13. Association Between Metformin and Sulfonylurea Monotherapies and Cancer Incidence: A Real-World Cohort Study in Shanghai, China.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2019
    Article
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  15. Anti-Diabetic Drugs: Cure or Risk Factors for Cancer?Pathology oncology research : POR · 2018
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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

19 authors at 5 institutions in 2 countries.

Cuiling QiVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China. These authors contributed equally to this work.
Qin ZhouVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China. These authors contributed equally to this work.
Bin LiVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Yang YangVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Liu CaoKey Laboratory of Medical Cell Biology, China Medical University, He Ping District, Shen Yang City, Liao Ning Province, China.
Yuxiang YeVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Jiangchao LiVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Yi DingVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Huiping WangVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Jintao WangVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Xiaodong HeVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Qianqian ZhangVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Tian LanVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Kenneth Ka Ho LeeKey Laboratory for Regenerative Medicine of the Ministry of Education, School of Biomedical Sciences, Chinese University of Hong Kong, Shatin, Hong Kong, China.
Weidong LiVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Xiaoyu SongKey Laboratory of Medical Cell Biology, China Medical University, He Ping District, Shen Yang City, Liao Ning Province, China.
Jia ZhouChemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX, United States.
Xuesong YangKey Laboratory for Regenerative Medicine of the Ministry of Education, Division of Histology & Embryology, Medical College, Jinan University, Guangzhou, China.
Lijing WangVascular Biology Research Institute, Guangdong Pharmaceutical University, Guangzhou, China.
Guangdong Pharmaceutical University · CNChina Medical University · CNChinese University of Hong Kong · CNJinan University · CNThe University of Texas Medical Branch at Galveston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is involved in the development, progression and metastasis of various human cancers. Herein, we report the discovery of glipizide, a widely used drug for type 2 diabetes mellitus, as a promising anticancer agent through the inhibition of tumor angiogenesis. By high-throughput screening (HTS) of an FDA approved drug library utilizing our in vivo chick embryo chorioallantoic membrane (CAM) and yolk sac membrane (YSM) models, glipizide has been identified to significantly inhibit blood vessel formation and development. Moreover, glipizide was found to suppress tumor angiogenesis, tumor growth and metastasis using xenograft tumor and MMTV-PyMT transgenic mouse models. We further revealed that the anticancer capability of glipizide is not attributed to its antiproliferative effects, which are not significant against various human cancer cell lines. To investigate whether its anticancer efficacy is associated with the glucose level alteration induced by glipizide application, glimepiride, another medium to long-acting sulfonylurea antidiabetic drug in the same class, was employed for the comparison studies in the same fashion. Interestingly, glimepiride has demonstrated no significant impact on the tumor growth and metastasis, indicating that the anticancer effects of glipizide is not ascribed to its antidiabetic properties. Furthermore, glipizide suppresses endothelial cell migration and the formation of tubular structures, thereby inhibiting angiogenesis by up-regulating the expression of natriuretic peptide receptor A. These findings uncover a novel mechanism of glipizide as a potential cancer therapy, and also for the first time, provide direct evidence to support that treatment with glipizide may reduce the cancer risk for diabetic patients.

Indexed as

Angiogenesis InhibitorsAnimalsBreast NeoplasmsCell Line, TumorCell ProliferationChick EmbryoChorioallantoic MembraneDisease Models, AnimalFemaleGlipizideHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsHypoglycemic AgentsMammary Neoplasms, ExperimentalMCF-7 CellsAngiogenesis InhibitorsGlipizideHypoglycemic Agents

Identifiers

PMID25294818
PMCPMC4259451
OpenAlexW1527814995

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.