Evidence map›Paper›PMID 30010249›Full record

ArticleJournal of cellular and molecular medicine2018

Dipalmitoylphosphatidic acid inhibits breast cancer growth by suppressing angiogenesis via inhibition of the CUX1/FGF1/HGF signalling pathway.

Jian Chen, Zijun Zhou, Yuying Yao, Jianwei Dai, Dalei Zhou, Lijing Wang, Qian-Qian Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

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  6. Chicken embryo model forInternational journal of pharmaceutics: X · 2023
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  11. miR-143-3p inhibits proliferation and invasion of hepatocellular carcinoma cells by regulating its target gene FGF1.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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

7 authors at 2 institutions in 1 country.

Jian ChenVascular Biology Research Institute, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, China.
Zijun ZhouVascular Biology Research Institute, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, China.
Yuying YaoVascular Biology Research Institute, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, China.
Jianwei DaiGMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, China.
Dalei ZhouVascular Biology Research Institute, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, China.
Lijing WangVascular Biology Research Institute, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, China.
Qian-Qian ZhangVascular Biology Research Institute, School of Basic Course, Guangdong Pharmaceutical University, Guangzhou, China.ORCID 0000-0001-6481-0780
Guangdong Pharmaceutical University · CNFirst Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour growth depends on a continual supply of the nutrients and oxygen, which are offered by tumour angiogenesis. Our previous study showed that dipalmitoylphosphatidic acid (DPPA), a bioactive phospholipid, inhibits the growth of triple-negative breast cancer cells. However, its direct effect on angiogenesis remains unknown. Our work showed that DPPA significantly suppressed vascular growth in the chick embryo chorioallantoic membrane (CAM) and yolk sac membrane (YSM) models. Meanwhile, tumour angiogenesis and tumour growth were inhibited by DPPA in the tumour tissues of an experimental breast cancer model, a subcutaneous xenograft mouse model and a genetically engineered spontaneous breast cancer mouse model (MMTV-PyMT). Furthermore, DPPA directly inhibited the proliferation, migration and tube formation of vascular endothelial cells. The anti-angiogenic effect of DPPA was regulated by the inhibition of Cut-like homeobox1 (CUX1), which transcriptionally inhibited fibroblast growth factor 1 (FGF1), leading to the downregulation of hepatocyte growth factor (HGF). This work first demonstrates that DPPA directly inhibits angiogenesis in cancer development. Our previous work along with this study suggest that DPPA functions as an anti-tumour therapeutic drug that inhibits angiogenesis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationChick EmbryoChorioallantoic MembraneFemaleFibroblast Growth Factor 1Hepatocyte Growth FactorHomeodomain ProteinsHumansHuman Umbilical Vein Endothelial CellsMammary Neoplasms, ExperimentalMiceAntineoplastic AgentsCUX1 protein, humandipalmitoylphosphatidic acidFibroblast Growth Factor 1Hepatocyte Growth FactorHomeodomain ProteinsNuclear ProteinsPhosphatidic AcidsRepressor ProteinsTranscription Factorsangiogenesisbreast cancerCUX1/FGF1/HGF signallingdipalmitoylphosphatidic acid

Identifiers

PMID30010249
PMCPMC6156235
OpenAlexW2883500876

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.