Evidence map›Paper›PMID 27584043›Full record

ArticleJournal of visualized experiments : JoVE2016

An Orthotopic Mouse Model of Spontaneous Breast Cancer Metastasis.

Amy V Paschall, Kebin Liu

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 13% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Frontiers in oncology · 2021
    Pooled it
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  7. Review
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  10. FZD7 expression marks mammary tumor-initiating cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Between Prometheus and Thanatos: Reflections on Intracardiac Injection Models for Metastasis in Mice.Journal of the American Association for Laboratory Animal Science : JAALAS · 2025
    Review
  12. Article
  13. Review
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4 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

2 authors at 1 institution in 1 country.

Amy V PaschallDepartment of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University; Georgia Cancer Center, Augusta University; Charlie Norwood VA Medical Center.
Kebin LiuDepartment of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University; Georgia Cancer Center, Augusta University; Charlie Norwood VA Medical Center; Kliu@gru.edu.
Augusta University · US

Funding

Role of IRF8 in Tumor Rejection and SuppressionR01CA133085 · NCI · AUGUSTA UNIVERSITY · PI LIU, KEBIN · 2008 to 2019
$2.9M
Role of NF-kB in Fas-mediated Apoptosis and Tumor SuppressionR01CA182518 · NCI · AUGUSTA UNIVERSITY · PI LIU, KEBIN · 2014 to 2018
$1.6M
H3K9 Methylation and Pancreatic Cancer ChemoresistanceR21CA185909 · NCI · AUGUSTA UNIVERSITY · PI LIU, KEBIN · 2014 to 2015
$362k
Function of IRF8 in MDSC and T Cell DifferentiationF31AI120487 · NIAID · AUGUSTA UNIVERSITY · PI PASCHALL, AMY · 2016 to 2016
$32k
Function of Verticillin A in Suppression of MDSC and CRC Stem CellsI01BX001962 · VA · CHARLIE NORWOOD VA MEDICAL CENTER · PI LIU, KEBIN · 2014 to 2017
–
BLRD VA I01 BX001962NCI NIH HHS R01 CA133085NCI NIH HHS R01 CA182518NCI NIH HHS R21 CA185909NIAID NIH HHS F31 AI120487
6 · The paper itself

Abstract

Metastasis is the primary cause of mortality of breast cancer patients. The mechanism underlying cancer cell metastasis, including breast cancer metastasis, is largely unknown and is a focus in cancer research. Various breast cancer spontaneous metastasis mouse models have been established. Here, we report a simplified procedure to establish orthotopic transplanted breast cancer primary tumor and resultant spontaneous metastasis that mimic human breast cancer metastasis. Combined with the bioluminescence live tumor imaging, this mouse model allows tumor growth and progression kinetics to be monitored and quantified. In this model, a low dose (1 x 10(4) cells) of 4T1-Luc breast cancer cells was injected into BALB/c mouse mammary fat pad using a tuberculin syringe. Mice were injected with luciferin and imaged at various time points using a bioluminescent imaging system. When the primary tumors grew to the size limit as in the IACUC-approved protocol (approximately 30 days), mice were anesthetized under constant flow of 2% isoflurane and oxygen. The tumor area was sterilized with 70% ethanol. The mouse skin around the tumor was excised to expose the tumor which was removed with a pair of sterile scissors. Removal of the primary tumor extends the survival of the 4T-1 tumor-bearing mice for one month. The mice were then repeatedly imaged for metastatic tumor spreading to distant organs. Therapeutic agents can be administered to suppress tumor metastasis at this point. This model is simple and yet sensitive in quantifying breast cancer cell growth in the primary site and progression kinetics to distant organs, and thus is an excellent model for studying breast cancer growth and progression, and for testing anti-metastasis therapeutic and immunotherapeutic agents in vivo.

Indexed as

Disease Models, AnimalNeoplasm MetastasisAnimalsBreastBreast NeoplasmsCell Line, TumorHumansMiceMice, Inbred BALB C

Identifiers

PMID27584043
PMCPMC5091834
OpenAlexW2511964116

What OpenQuestion holds

Textmetadata
LicenceTDM
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.