2020
DOI: 10.1007/s10911-020-09469-w
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Intraductal Injection of Lentivirus Vectors for Stably Introducing Genes into Rat Mammary Epithelial Cells in Vivo

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Cited by 12 publications
(5 citation statements)
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“…5 C ) . Genetic engineering has further paved the way for models recapitulating specific molecular BC subtypes and mutational signatures, and for studying the impact of specific germline or somatic mutations in tumor suppressor genes or oncogenes associated with BC [ 262 , 270 , 303 , 304 ], such as the creation of rats with germline Nf1 mutations using CRISPR/Cas9 gene editing [ 270 ] ( Fig. 5 F ) .…”
Section: Applicationsmentioning
confidence: 99%
See 1 more Smart Citation
“…5 C ) . Genetic engineering has further paved the way for models recapitulating specific molecular BC subtypes and mutational signatures, and for studying the impact of specific germline or somatic mutations in tumor suppressor genes or oncogenes associated with BC [ 262 , 270 , 303 , 304 ], such as the creation of rats with germline Nf1 mutations using CRISPR/Cas9 gene editing [ 270 ] ( Fig. 5 F ) .…”
Section: Applicationsmentioning
confidence: 99%
“…Such a tool enables specific anatomical targeting with the retroviral constructs, which only incorporate into the genome of proliferating mammary ductal epithelial cells [258]. In addition to retroviruses, lentivirus and adeno-associated virus (AAV) vectors can be used to deliver genetic content and trigger in situ genome editing in rats, as done in mouse models [100,262].…”
Section: Genetically Engineered Rat Mammary Tumor Modelsmentioning
confidence: 99%
“…At the same time, one might wonder how well these models currently recapitulate human physiology. As just one example, it has been notoriously difficult to model ER + breast cancer in GEMMs, which is why some labs are now – also aided by the developments in genome editing technology – switching to rats [ 158 , 159 ].…”
Section: Five Challenges For the Next Decadementioning
confidence: 99%
“…Therefore, intraductal injection of a virus carrying gRNA could be used to mutate NF1 and other genes associated with human ER+ cancer to generate somatic models of ER+ cancer in rats. Wen and Yi also described the intraductal injection of lentiviral vector FUCGW carrying the mutated oncogene HrasQ61L to Sprague/Dawley rats led to mammary tumors with high positive expression of both ER and PR ( 124 ). This technique is an efficient tool for modeling formation, prevention, and treatment of human breast cancer, especially ER+ breast cancer.…”
Section: Challenges In Modeling Er+ Breast Cancermentioning
confidence: 99%