Evidence map›Paper›PMID 22689061›Full record

ArticleOncogene2013

YAP modifies cancer cell sensitivity to EGFR and survivin inhibitors and is negatively regulated by the non-receptor type protein tyrosine phosphatase 14.

J-M Huang, I Nagatomo, E Suzuki, T Mizuno, T Kumagai, A Berezov, H Zhang, B Karlan, M I Greene, Q Wang

Abstract read
In one paragraph

Article in Oncogene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

97 citing papers in PubMed, 150 citations in OpenAlex.

  1. Yorkie/YAP Interactors: Fine-Tuning the Hippo Pathway Output.Cold Spring Harbor perspectives in biology · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. HPV18 E7 inhibits LATS1 kinase and activates YAP1 by degrading PTPN14.bioRxiv : the preprint server for biology · 2024
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Complex roles of Hippo-YAP/TAZ signaling in hepatocellular carcinoma.Journal of cancer research and clinical oncology · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. An overview of the crosstalk between YAP and cGAS-STING signaling in non-small cell lung cancer: it takes two to tango.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  18. Article
  19. Review
  20. Review

37 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

10 authors at 2 institutions in 1 country.

J-M HuangCedars-Sinai Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute Los Angeles, CA 90048, USA.
I Nagatomo
E Suzuki
T Mizuno
T Kumagai
A Berezov
H Zhang
B Karlan
M I Greene
Q Wang
Cedars-Sinai Medical Center · USUniversity of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Rebecca A Simmons · 2006 to 2026
$35.3M
RECEPTOR MEDIATED BREAST CANCER THERAPYR01CA089481 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GREENE, MARK I · 2001 to 2015
$3.3M
IMMUNOBIOLOGY OF P185 RECEPTORR01CA055306 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GREENE, MARK I · 1992 to 2011
$2.6M
NCI NIH HHS P30 CA016520NCI NIH HHS P30CA016520NCI NIH HHS R01 CA055306NCI NIH HHS R01 CA089481NCI NIH HHS R01CA089481NIEHS NIH HHS ES013508-04NIEHS NIH HHS P30 ES013508
6 · The paper itself

Abstract

The Yes-associated protein (YAP) is a transcriptional factor involved in tissue development and tumorigenesis. Although YAP has been recognized as a key element of the Hippo signaling pathway, the mechanisms that regulate YAP activities remain to be fully characterized. In this study, we demonstrate that the non-receptor type protein tyrosine phosphatase 14 (PTPN14) functions as a negative regulator of YAP. We show that YAP forms a protein complex with PTPN14 through the WW domains of YAP and the PPXY motifs of PTPN14. In addition, PTPN14 inhibits YAP-mediated transcriptional activities. Knockdown of YAP sensitizes cancer cells to various anti-cancer agents, such as cisplatin, the EGFR tyrosine kinase inhibitor erlotinib and the small-molecule antagonist of survivin, S12. YAP-targeted modalities may be used in combination with other cancer drugs to achieve maximal therapeutic effects.

Indexed as

AcyltransferasesAdaptor Proteins, Signal TransducingAmino Acid MotifsAnimalsAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationCisplatinErbB ReceptorsErlotinib HydrochlorideGene Knockdown TechniquesGenes, ReporterHEK293 CellsHumansInhibitor of Apoptosis ProteinsAcyltransferasesAdaptor Proteins, Signal TransducingAntineoplastic AgentsBIRC5 protein, humanCisplatinErbB ReceptorsErlotinib HydrochlorideInhibitor of Apoptosis ProteinsLuciferases, RenillaPeptide FragmentsPhosphoproteinsProtein Tyrosine Phosphatases, Non-ReceptorPTPN14 protein, humanQuinazolinesRNA, Small InterferingSurvivinTAFAZZIN protein, humanTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID22689061
PMCPMC3443515
OpenAlexW1993246426

What OpenQuestion holds

Textmetadata
LicenceTDM
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.