Evidence map›Paper›PMID 23733356›Full record

ArticleGenesis (New York, N.Y. : 2000)2013

The ortholog of the human proto-oncogene ROS1 is required for epithelial development in C. elegans.

Martin R Jones, Ann M Rose, David L Baillie

Open access · hybridAbstract read
In one paragraph

Article in Genesis (New York, N.Y. : 2000), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Pathways that affect anterior morphogenesis inbioRxiv : the preprint server for biology · 2023
    Article
  2. 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

3 authors at 2 institutions in 1 country.

Martin R JonesDepartment of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada, V6T 1Z4. jonesmr@mail.ubc.ca
Ann M Rose
David L Baillie
University of British Columbia · CASimon Fraser University · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The orphan receptor ROS1 is a human proto-oncogene, mutations of which are found in an increasing number of cancers. Little is known about the role of ROS1, however in vertebrates it has been implicated in promoting differentiation programs in specialized epithelial tissues. In this study we show that the C. elegans ortholog of ROS1, the receptor tyrosine kinase ROL-3, has an essential role in orchestrating the morphogenesis and development of specialized epidermal tissues, highlighting a potentially conserved function in coordinating crosstalk between developing epithelial cells. We also provide evidence of a direct relationship between ROL-3, the mucin SRAP-1, and BCC-1, the homolog of mRNA regulating protein Bicaudal-C. This study answers a longstanding question as to the developmental function of ROL-3, identifies three new genes that are expressed and function in the developing epithelium of C. elegans, and introduces the nematode as a potentially powerful model system for investigating the increasingly important, yet poorly understood, human oncogene ROS1.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEpitheliumMorphogenesisMucinsProto-Oncogene MasProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesCaenorhabditis elegans ProteinsMAS1 protein, humanMucinsProto-Oncogene MasProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesROL-3 protein, C elegansCaenorhabditis eleganscuticleepithelialROL-3ROS1 oncogeneseam cells

Identifiers

PMID23733356
PMCPMC4232869
OpenAlexW1553613614

What OpenQuestion holds

Textmetadata
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.