Evidence map›Paper›PMID 27993815›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2017

Differential gene expression profiling of matched primary renal cell carcinoma and metastases reveals upregulation of extracellular matrix genes.

T H Ho, D J Serie, M Parasramka, J C Cheville, B M Bot, W Tan, L Wang, R W Joseph, T Hilton, B C Leibovich and 2 more

Abstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

66 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  13. Lung Inflammatory Phenotype in Mice Deficient in Fibulin-2 and ADAMTS-12.International journal of molecular sciences · 2024
    Article
  14. Article
  15. Metformin suppresses proliferation and glycolysis of gastric cancer by modulating ADAMTS12.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2024
    Article
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  17. Review
  18. HOOK1 Inhibits the Progression of Renal Cell Carcinoma via TGF-β and TNFSF13B/VEGF-A Axis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  19. Article
  20. Article

6 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

12 authors.

T H HoDivision of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, USA.
D J SerieDepartments of Health Sciences Research, Mayo Clinic, Jacksonville, FL, USA.
M ParasramkaCancer Biology, Mayo Clinic, Jacksonville, USA.
J C ChevilleLaboratory Medicine and Pathology, Mayo Clinic, Rochester, NY, USA.
B M BotComputational Oncology, Sage Bionetworks, Seattle, USA.
W TanDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL, USA.
L WangDepartment of Pathology, Medical College of Hebei University of Engineering, Handan, Hebei Province, China.
R W JosephDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL, USA.
T HiltonDepartments of Health Sciences Research, Mayo Clinic, Jacksonville, FL, USA.
B C LeibovichDepartment of Urology, Mayo Clinic, Rochester, USA.
A S ParkerDepartments of Health Sciences Research, Mayo Clinic, Jacksonville, FL, USA.
J E Eckel-PassowDepartment of Pathology, Medical College of Hebei University of Engineering, Handan, Hebei Province, China.

Funding

Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
Design and Validation of a Biomarker-enhanced System to Predict RCC ProgressionR01CA134466 · NCI · MAYO CLINIC JACKSONVILLE · PI PARKER, ALEXANDER S · 2010 to 2014
$1.7M
Evaluation of Patient-Matched Primary and Metastatic Samples to Identify and ValiR21CA176422 · NCI · MAYO CLINIC ROCHESTER · PI ECKEL PASSOW, JEANETTE E · 2013 to 2014
$390k
NCI NIH HHS K12 CA090628NCI NIH HHS R01 CA134466NCI NIH HHS R21 CA176422
6 · The paper itself

Abstract

Background: The majority of renal cell carcinoma (RCC) studies analyze primary tumors, and the corresponding results are extrapolated to metastatic RCC tumors. However, it is unknown if gene expression profiles from primary RCC tumors differs from patient-matched metastatic tumors. Thus, we sought to identify differentially expressed genes between patient-matched primary and metastatic RCC tumors in order to understand the molecular mechanisms underlying the development of RCC metastases. Patients and methods: We compared gene expression profiles between patient-matched primary and metastatic RCC tumors using a two-stage design. First, we used Affymetrix microarrays on 15 pairs of primary RCC [14 clear cell RCC (ccRCC), 1 papillary] tumors and patient-matched pulmonary metastases. Second, we used a custom NanoString panel to validate seven candidate genes in an independent cohort of 114 ccRCC patients. Differential gene expression was evaluated using a mixed effect linear model; a random effect denoting patient was included to account for the paired data. Third, The Cancer Genome Atlas (TCGA) data were used to evaluate associations with metastasis-free and overall survival in primary ccRCC tumors. Results: We identified and validated up regulation of seven genes functionally involved in the formation of the extracellular matrix (ECM): DCN, SLIT2, LUM, LAMA2, ADAMTS12, CEACAM6 and LMO3. In primary ccRCC, CEACAM6 and LUM were significantly associated with metastasis-free and overall survival (P < 0.01). Conclusions: We evaluated gene expression profiles using the largest set to date, to our knowledge, of patient-matched primary and metastatic ccRCC tumors and identified up regulation of ECM genes in metastases. Our study implicates up regulation of ECM genes as a critical molecular event leading to visceral, bone and soft tissue metastases in ccRCC.

Indexed as

ADAMTS ProteinsAdaptor Proteins, Signal TransducingAdultAgedAntigens, CDBiomarkers, TumorCarcinoma, Renal CellCell Adhesion MoleculesDecorinDisease-Free SurvivalExtracellular MatrixFemaleGene Expression Regulation, NeoplasticGPI-Linked ProteinsHumansIntercellular Signaling Peptides and ProteinsADAMTS12 protein, humanADAMTS ProteinsAdaptor Proteins, Signal TransducingAntigens, CDBiomarkers, TumorCEACAM6 protein, humanCell Adhesion MoleculesDCN protein, humanDecorinGPI-Linked ProteinsIntercellular Signaling Peptides and ProteinsLamininlaminin alpha 2LIM Domain ProteinsLMO3 protein, humanLumicanLUM protein, humanNerve Tissue ProteinsSlit Homolog 2 Proteinextracellular matrixmetastasesrenal cell carcinoma

Identifiers

PMID27993815
PMCPMC5834119

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.