Evidence map›Paper›PMID 28002618›Full record

ArticleCancer science2017

Verteporfin suppresses cell survival, angiogenesis and vasculogenic mimicry of pancreatic ductal adenocarcinoma via disrupting the YAP-TEAD complex.

Honglong Wei, Fuhai Wang, Yong Wang, Tao Li, Peng Xiu, Jingtao Zhong, Xueying Sun, Jie Li

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

134 citing papers in PubMed, 209 citations in OpenAlex.

  1. Review
  2. More than a ring: the emerging role of heme in angiogenesis.Cell communication and signaling : CCS · 2026
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  12. Targeting yes-associated protein to overcome imatinib resistance in gastrointestinal stromal tumor drug-tolerant persister cells.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2025
    Article
  13. Review
  14. Article
  15. Targeted silencing of Engrailed-1 reprograms profibrotic fibroblast lineage for scarless wound healing.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  16. Review
  17. Murine Cell Line Models for Vascular Mimicry: The Role of YAP/TAZ Signaling.International journal of molecular sciences · 2025
    Article
  18. Article
  19. Review
  20. Article

74 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 2 countries.

Honglong WeiDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Fuhai WangDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Yong WangDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Tao LiDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Peng XiuDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Jingtao ZhongDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Xueying SunDepartment of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Jie LiDepartment of General Surgery, Qianfoshan Hospital, Shandong University, Jinan, China.
Shandong Provincial QianFoShan Hospital · CNShandong University · CNUniversity of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive human malignancies. The Yes-associated protein-1 (YAP) plays a critical role in cell proliferation, apoptosis and angiogenesis. Verteporfin is a photosensitizer used in photodynamic therapy and also a small molecular inhibitor of the Hippo-YAP pathway. However, little is known about whether verteporfin could inhibit YAP activity in PDAC cells. Our present results showed that verteporfin suppressed the proliferation of human PDAC PANC-1 and SW1990 cells by arresting cells at the G1 phase, and inducing apoptosis in dose- and time-dependent manners. Verteporfin also inhibited the tumor growth on the PDAC xenograft model. Treatment with verteporfin led to downregulation of cyclinD1 and cyclinE1, modulation of Bcl-2 family proteins and activation of PARP. In addition, verteporfin exhibited an inhibitory effect on angiogenesis and vasculogenic mimicry via suppressing Ang2, MMP2, VE-cadherin, and α-SMA expression in vitro and in vivo. Mechanism studies demonstrated that verteporfin impaired YAP and TEAD interaction to suppress the expression of targeted genes. Our results provide a foundation for repurposing verteporfin as a promising anti-tumor drug in the treatment of pancreatic cancer by targeting the Hippo pathway.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAntigens, CDAntineoplastic AgentsApoptosisCadherin 5CadherinsCarcinoma, Pancreatic DuctalCell Line, TumorCell ProliferationCell SurvivalCyclin D1Cyclin EDNA-Binding ProteinsG1 Phase Cell Cycle CheckpointsHumansAdaptor Proteins, Signal TransducingAntigens, CDAntineoplastic AgentsCadherin 5CadherinsCCND1 protein, humanCCNE1 protein, humanCyclin D1Cyclin EDNA-Binding ProteinsMatrix Metalloproteinase 2MMP2 protein, humanNuclear ProteinsOncogene ProteinsPARP1 protein, humanPhosphoproteinsPoly (ADP-Ribose) Polymerase-1PorphyrinsProto-Oncogene Proteins c-bcl-2TEAD1 protein, humanTEA Domain Transcription FactorsTranscription FactorsVerteporfinVesicular Transport ProteinsVPS51 protein, humanYAP1 protein, humanYAP-Signaling ProteinsAngiogenesisapoptosispancreatic cancervasculogenic mimicryverteporfin

Identifiers

PMID28002618
PMCPMC5378285
OpenAlexW2565295747

What OpenQuestion holds

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LicenceCC BY-NC
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.