Evidence map›Paper›PMID 28448047›Full record

ArticleJournal of visualized experiments : JoVE2017

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies.

Katherine A Murphy, Britnie R James, Andrew Wilber, Thomas S Griffith

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. ITM2B Truncation Promotes Migrasome Formation to Accelerate Renal Cell Carcinoma Growth.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

4 authors at 2 institutions in 2 countries.

Katherine A MurphyDepartment of Urology, University of Minnesota; Masonic Cancer Center, University of Minnesota.
Britnie R JamesDepartment of Urology, University of Minnesota; Masonic Cancer Center, University of Minnesota; Microbiology, Immunology, and Cancer Biology Graduate Program, University of Minnesota.
Andrew WilberDepartment of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine; Simmons Cancer Institute.
Thomas S GriffithDepartment of Urology, University of Minnesota; Masonic Cancer Center, University of Minnesota; Microbiology, Immunology, and Cancer Biology Graduate Program, University of Minnesota; tgriffit@umn.edu.
University of Minnesota · USSimmons University · US

Funding

TRAIL-expressing Recombinant Adenovirus Based Immunotherapy for RCCR01CA109446 · NCI · UNIVERSITY OF MINNESOTA · PI GRIFFITH, THOMAS S · 2004 to 2013
$2.6M
Renal Cell Tumor-Mediated Trans-differentiation of Natural Killer CellsR15CA173657 · NCI · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI WILBER, ANDREW CHRISTROPHER · 2013 to 2013
$375k
NCI NIH HHS R01 CA109446NCI NIH HHS R15 CA173657
6 · The paper itself

Abstract

Renal cell carcinoma (RCC) affects > 60,000 people in the United States annually, and ~ 30% of RCC patients have multiple metastases at the time of diagnosis. Metastatic RCC (mRCC) is incurable, with a median survival time of only 18 months. Immune-based interventions (e.g., interferon (IFN) and interleukin (IL)-2) induce durable responses in a fraction of mRCC patients, and multikinase inhibitors (e.g., sunitinib or sorafenib) or anti-VEGF receptor monoclonal antibodies (mAb) are largely palliative, as complete remissions are rare. Such shortcomings in current therapies for mRCC patients provide the rationale for the development of novel treatment protocols. A key component in the preclinical testing of new therapies for mRCC is a suitable animal model. Beneficial features that recapitulate the human condition include a primary renal tumor, renal tumor metastases, and an intact immune system to investigate any therapy-driven immune effector responses and the formation of tumor-induced immunosuppressive factors. This report describes an orthotopic mRCC mouse model that has all of these features. We describe an intrarenal implantation technique using the mouse renal adenocarcinoma cell line Renca, followed by the assessment of tumor growth in the kidney (primary site) and lungs (metastatic site).

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, Renal CellDisease Models, AnimalDrug Evaluation, PreclinicalKidney NeoplasmsMiceNeoplasms, ExperimentalAntineoplastic Agents

Identifiers

PMID28448047
PMCPMC5564692
OpenAlexW2607116009

What OpenQuestion holds

Textmetadata
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.