Evidence map›Paper›PMID 27336605›Full record

ArticleBritish journal of cancer2016

WW domain binding protein 5 induces multidrug resistance of small cell lung cancer under the regulation of miR-335 through the Hippo pathway.

Ruixiang Tang, Yingying Lei, Bingshuang Hu, Jie Yang, Shun Fang, Qiongyao Wang, Man Li, Linlang Guo

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Cancers · 2025
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  4. Review
  5. Article
  6. Review
  7. Article
  8. Functions and Targets of miR-335 in Cancer.OncoTargets and therapy · 2021
    Review
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  11. Review
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  19. Article
  20. The Ambivalent Function of YAP in Apoptosis and Cancer.International journal of molecular sciences · 2018
    Review
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 2 institutions in 1 country.

Ruixiang TangDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yingying LeiDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Bingshuang HuDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Jie YangDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Shun FangDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Qiongyao WangDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Man LiDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Linlang GuoDepartment of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Southern Medical University · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur previous study indicated that WW domain binding protein 5 (WBP5) expression was elevated significantly in a drug-resistant cell compared with its parental cell. Nevertheless, its functional role and underlying mechanisms remain unknown.

methodsIn this study, WBP5 was examined in 62 small cell lung cancer (SCLC) patient samples by immunohistochemical technique. Stable WBP5-overexpressed and WBP5-underexpressed cells were further established to assess the role of WBP5 in drug resistance, apoptosis and tumour growth. We also conducted western blot to detect the expression of MST2 and YAP1 and their phosphorylated protein.

resultsThe results revealed that WBP5 expression was significantly associated with the shorter survival time in SCLC patients. Upregulation of WBP5 induced multidrug resistance (MDR) and decreased apoptosis, whereas downregulation of WBP5 enhanced drug sensitivity and increased apoptosis. We also found that miR-335 negatively regulated the MDR of WBP5 by targeting its 3'UTR. Furthermore, WBP5 can lower YAP1 phosphorylation at Serine 127 and induce nuclear accumulation of YAP1. Inhibition of YAP1 by Verteporfin could blunt the MDR phenotype of WBP5.

conclusionsWW domain binding protein 5 can modulate MDR through the Hippo pathway under the regulation of miR-335. WW domain binding protein 5 may be a prognostic predictor and a potential target for interfering with MDR in SCLC.

Indexed as

Antineoplastic AgentsCell Line, TumorDrug Resistance, MultipleDrug Resistance, NeoplasmFemaleHippo Signaling PathwayHumansLung NeoplasmsMaleMicroRNAsNeoplasm StagingPrognosisProtein Serine-Threonine KinasesSmall Cell Lung CarcinomaSurvival AnalysisAntineoplastic AgentsMicroRNAsMIRN155 microRNA, humanProtein Serine-Threonine Kinases

Identifiers

PMID27336605
PMCPMC4947702
OpenAlexW2472263228

What OpenQuestion holds

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Registered trials

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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.