Evidence map›Paper›PMID 26289340›Full record

ArticleScientific reports2015

Ductal activation of oncogenic KRAS alone induces sarcomatoid phenotype.

Yong Fu, Zobeida Cruz-Monserrate, H Helen Lin, Yiyin Chung, Baoan Ji, Szu-Min Lin, Steven Vonderfecht, Craig D Logsdon, Chien-Feng Li, David K Ann

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Current State of Knowledge on Salivary Gland Cancers.Critical reviews in oncogenesis · 2018
    Review
  9. Article
  10. Article
  11. 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

10 authors at 4 institutions in 2 countries.

Yong FuDepartment of Diabetes and Metabolic Diseases Research, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Zobeida Cruz-MonserrateDepartment of Cancer Biology, UT MD Anderson Cancer Center, Houston, Texas 77054, USA.
H Helen LinMolecular and Cellular Biology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Yiyin ChungDepartment of Diabetes and Metabolic Diseases Research, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Baoan JiMayo Clinic, Rochester, Minnesota.
Szu-Min LinDepartment of Diabetes and Metabolic Diseases Research, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Steven VonderfechtShared Research Animal Resources, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Craig D LogsdonDepartment of Cancer Biology, UT MD Anderson Cancer Center, Houston, Texas 77054, USA.
Chien-Feng LiDepartment of Pathology, Chi-Mei Medical Center, Tainan, Taiwan.
David K AnnDepartment of Diabetes and Metabolic Diseases Research, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Beckman Research InstituteThe University of Texas MD Anderson Cancer Center · USChi Mei Medical Center · TWMayo Clinic · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
MOLECULAR PROGRAMMING OF SALIVARY GLAND GENE EXPRESSIONR01DE010742 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ANN, DAVID K. · 1993 to 2013
$5.1M
MOLECULAR MECHANISMS OF PANCREATITISR01DK052067 · NIDDK · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGSDON, CRAIG D · 1998 to 2015
$4.4M
Mechanisms for Salivary Tumor Epithelial-Mesenchymal TransitionsR01DE026304 · NIDCR · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ANN, DAVID K., LIN, HER HELEN · 2016 to 2020
$2.1M
Molecular Characterization of Autophagy in Salivary Gland TumorsR21DE023298 · NIDCR · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ANN, DAVID K. · 2013 to 2014
$462k
NCI NIH HHS P30 CA016672NIDCR NIH HHS R01 DE010742NIDCR NIH HHS R01 DE026304NIDCR NIH HHS R01DE10742NIDCR NIH HHS R21 DE023298NIDCR NIH HHS R21DE023298NIDDK NIH HHS DK052067-08NIDDK NIH HHS R01 DK052067
6 · The paper itself

Abstract

Salivary duct carcinoma (SDC) is an uncommon, but aggressive malignant tumor with a high mortality rate. Herein, we reported the detection of somatic KRAS A146T and Q61H mutations in 2 out of 4 (50%) sarcomatoid SDC variants. Transgenic mice carrying the human oncogenic KRAS(G12V), which spatiotemporal activation by tamoxifen (TAM)-inducible Cre recombinase Ela-CreERT in the submandibular gland (SMG) ductal cells, was established and characterized. Visible carcinoma was detected as early as day-15 following oncogenic KRAS(G12V) induction alone, and these tumors proliferate rapidly with a median survival of 28-days accompanied with histological reminiscences to human sarcomatoid SDC variants. Moreover, these tumors were resistant to cetuximab treatment despite augmented EGFR signaling, attesting its malignancy. Our findings suggest that LGL-KRas(G12V);Ela-CreERT transgenic mice could serve as a useful preclinical model for investigating underlying mechanisms and developing potential therapies.

Indexed as

AdultAgedAged, 80 and overCell ProliferationCetuximabDrug Resistance, NeoplasmErbB ReceptorsFemaleHumansMaleMiddle AgedMutationPhenotypeProto-Oncogene Proteins p21(ras)Salivary DuctsSalivary Gland NeoplasmsCetuximabErbB ReceptorsKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID26289340
PMCPMC4642517
OpenAlexW1890472101

What OpenQuestion holds

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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.