Evidence map›Paper›PMID 28459465›Full record

ArticleOncogene2017

INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma.

N Yang, E L-H Leung, C Liu, L Li, T Eguether, X-J Jun Yao, E C Jones, D A Norris, A Liu, R A Clark and 4 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Hexa-Longin domain scaffolds for inter-Rab signalling.Bioinformatics (Oxford, England) · 2020
    Article
  12. Review
  13. CEP164 Deficiency Causes Hyperproliferation of Pancreatic Cancer Cells.Frontiers in cell and developmental biology · 2020
    Article
  14. Review
  15. Review
  16. Ciliary signalling in cancer.Nature reviews. Cancer · 2018
    Review
  17. Article
  18. Article
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

14 authors at 6 institutions in 3 countries.

N YangDepartment of Pathology, Stony Brook University, Stony Brook, NY, USA.
E L-H LeungState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
C LiuDepartment of Pathology, Stony Brook University, Stony Brook, NY, USA.
L LiDepartment of Dermatology, Peking Union Medical College Hospital, Beijing, China.
T EguetherProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
X-J Jun YaoState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
E C JonesDepartment of Dermatology, Stony Brook University, Stony Brook, NY, USA.
D A NorrisCharles C. Gates Center for Regenerative Medicine, University of Colorado Denver, Aurora, CO, USA.
A LiuDepartment of Biology, Eberly College of Science, Pennsylvania State University, University Park, PA, USA.
R A ClarkDepartment of Dermatology, Stony Brook University, Stony Brook, NY, USA.
D R RoopCharles C. Gates Center for Regenerative Medicine, University of Colorado Denver, Aurora, CO, USA.
G J PazourProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
K R ShroyerDepartment of Pathology, Stony Brook University, Stony Brook, NY, USA.
J ChenDepartment of Pathology, Stony Brook University, Stony Brook, NY, USA.
Stony Brook University · USMacau University of Science and Technology · MOGates (United States) · USUniversity of Massachusetts Chan Medical School · USPeking Union Medical College Hospital · CNPennsylvania State University · US

Funding

Intraflagellar Transport Proteins in MiceR01GM060992 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Gregory J Pazour · 2001 to 2026
$10.3M
TARGETING ONCOGENE EXPRESSION TO SKIN IN TRANSGENIC MICER01CA052607 · NCI · UNIVERSITY OF COLORADO DENVER · PI ROOP, DENNIS · 1990 to 2015
$6.5M
Transgenic and Gene Targeting CoreP30AR057212 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI NORRIS, DAVID A. · 2009 to 2018
$6.2M
Planar Cell Polarity Signaling in Hair Follicle FormationR01AR061485 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI CHEN, JIANG · 2011 to 2021
$3.8M
Establishing a Long Island Bioscience HubU01HL127522 · NHLBI · STATE UNIVERSITY NEW YORK STONY BROOK · PI RUBIN, CLINTON T · 2015 to 2017
$3.0M
The consequences of loricrin deficiency on epidermal barrier functionR01AR060388 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI REFAELI, YOSEF, ROOP, DENNIS · 2011 to 2015
$1.6M
NCI NIH HHS R01 CA052607NHLBI NIH HHS U01 HL127522NIAMS NIH HHS P30 AR057212NIAMS NIH HHS R01 AR060388NIAMS NIH HHS R01 AR061485NIGMS NIH HHS R01 GM060992
6 · The paper itself

Abstract

Inturned (INTU), a cilia and planar polarity effector, performs prominent ciliogenic functions during morphogenesis, such as in the skin. INTU is expressed in adult tissues but its role in tissue maintenance is unknown. Here, we report that the expression of the INTU gene is aberrantly elevated in human basal cell carcinoma (BCC), coinciding with increased primary cilia formation and activated hedgehog (Hh) signaling. Disrupting Intu in an oncogenic mutant Smo (SmoM2)-driven BCC mouse model prevented the formation of BCC through suppressing primary cilia formation and Hh signaling, suggesting that Intu performs a permissive role during BCC formation. INTU is essential for intraflagellar transport A complex assembly during ciliogenesis. To further determine whether Intu is directly involved in the activation of Hh signaling downstream of ciliogenesis, we examined the Hh signaling pathway in mouse embryonic fibroblasts, which readily responds to the Hh pathway activation. Depleting Intu blocked Smo agonist-induced Hh pathway activation, whereas the expression of Gli2ΔN, a constitutively active Gli2, restored Hh pathway activation in Intu-deficient cells, suggesting that INTU functions upstream of Gli2 activation. In contrast, overexpressing Intu did not promote ciliogenesis or Hh signaling. Taken together, data obtained from this study suggest that INTU is indispensable during BCC tumorigenesis and that its aberrant upregulation is likely a prerequisite for primary cilia formation during Hh-dependent tumorigenesis.

Indexed as

AnimalsBasal Cell CarcinomaCells, CulturedCiliaDisease Models, AnimalFemaleHedgehog ProteinsHumansMaleMembrane ProteinsMiceMice, TransgenicSignal TransductionSkin NeoplasmsTransfectionHedgehog Proteinsinturned protein, mouseMembrane Proteins

Identifiers

PMID28459465
PMCPMC5578876
OpenAlexW2610189799

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.