» Articles » PMID: 21263096

How Genetically Engineered Mouse Tumor Models Provide Insights into Human Cancers

Overview
Journal J Clin Oncol
Specialty Oncology
Date 2011 Jan 26
PMID 21263096
Citations 58
Authors
Affiliations
Soon will be listed here.
Abstract

Genetically engineered mouse models (GEMMs) of human cancer were first created nearly 30 years ago. These early transgenic models demonstrated that mouse cells could be transformed in vivo by expression of an oncogene. A new field emerged, dedicated to generating and using mouse models of human cancer to address a wide variety of questions in cancer biology. The aim of this review is to highlight the contributions of mouse models to the diagnosis and treatment of human cancers. Because of the breadth of the topic, we have selected representative examples of how GEMMs are clinically relevant rather than provided an exhaustive list of experiments. Today, as detailed here, sophisticated mouse models are being created to study many aspects of cancer biology, including but not limited to mechanisms of sensitivity and resistance to drug treatment, oncogene cooperation, early detection, and metastasis. Alternatives to GEMMs, such as chemically induced or spontaneous tumor models, are not discussed in this review.

Citing Articles

Characterization of A Bronchoscopically Induced Transgenic Lung Cancer Pig Model for Human Translatability.

Kaifi J, Joshi K, Suvilesh K, Natesh N, Manjunath Y, Coberly J Res Sq. 2025; .

PMID: 39975891 PMC: 11838710. DOI: 10.21203/rs.3.rs-5054204/v1.


Characterization of A Bronchoscopically Induced Transgenic Lung Cancer Pig Model for Human Translatability.

Joshi K, Suvilesh K, Natesh N, Manjunath Y, Coberly J, Schlink S bioRxiv. 2024; .

PMID: 39569144 PMC: 11577786. DOI: 10.1101/2024.11.04.621940.


Canine on the Couch: The New Canary in the Coal Mine for Environmental Health Research.

Wise C, Breen M, Stapleton H Environ Health (Wash). 2024; 2(8):517-529.

PMID: 39170948 PMC: 11334179. DOI: 10.1021/envhealth.4c00029.


Application status and future prospects of the PDX model in lung cancer.

Liu W, Cui Y, Zheng X, Yu K, Sun G Front Oncol. 2023; 13:1098581.

PMID: 37035154 PMC: 10080030. DOI: 10.3389/fonc.2023.1098581.


Novel Mouse Models for Cancer Immunology.

Connolly K, Fitzgerald B, Damo M, Joshi N Annu Rev Cancer Biol. 2023; 6(1):269-291.

PMID: 36875867 PMC: 9979244. DOI: 10.1146/annurev-cancerbio-070620-105523.


References
1.
Meylan E, Dooley A, Feldser D, Shen L, Turk E, OuYang C . Requirement for NF-kappaB signalling in a mouse model of lung adenocarcinoma. Nature. 2009; 462(7269):104-7. PMC: 2780341. DOI: 10.1038/nature08462. View

2.
Orsulic S . An RCAS-TVA-based approach to designer mouse models. Mamm Genome. 2002; 13(10):543-7. DOI: 10.1007/s00335-002-4003-4. View

3.
Zhou Y, Rideout 3rd W, Zi T, Bressel A, Reddypalli S, Rancourt R . Chimeric mouse tumor models reveal differences in pathway activation between ERBB family- and KRAS-dependent lung adenocarcinomas. Nat Biotechnol. 2009; 28(1):71-8. DOI: 10.1038/nbt.1595. View

4.
DuPage M, Dooley A, Jacks T . Conditional mouse lung cancer models using adenoviral or lentiviral delivery of Cre recombinase. Nat Protoc. 2009; 4(7):1064-72. PMC: 2757265. DOI: 10.1038/nprot.2009.95. View

5.
Pleasance E, Stephens P, OMeara S, McBride D, Meynert A, Jones D . A small-cell lung cancer genome with complex signatures of tobacco exposure. Nature. 2009; 463(7278):184-90. PMC: 2880489. DOI: 10.1038/nature08629. View