All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.
The transition of fallopian tube epithelial (FTE) cells to cancer cells originated from the TP53 gene mutation. The clonal expansion of the TP53 mutated cells can progress to FTE carcinoma and high-grade serous tubo-ovarian cancer (HGSCs). Genomic analysis of cancer cells demonstrates the various types of genetic abnormalities, including single nucleotide variants, gene deletion, copy number alterations, and gene silencing, which influence downstream gene expression and pathways. Poor response and resistance to current chemotherapy provoke the development of novel effective therapies for tumor treatment.
Creative Biolabs provides a platform for fallopian tube carcinoma cancer organoids with different genotypes for disease modeling and application to CAR therapy development.
Fig.1 Fallopian tube carcinoma cancer organoids establishment and characterization. (Yucer, et al., 2021)
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Reported Abnormal Genes | ||||
TP53 | BRCA1 | BRCA2 | Nf1 | RAD51 |
PTEN | EMSY | CCNE1 | MYC |
The cancer organoids are advanced and easily manipulate models for CAR-T in vitro anti-tumor efficacy evaluations. Creative Biolabs provides the following cancer antigen-related products that could be used in CAR-T construction and examination assays.
Target Antigen | Target Description | CAR-T Products |
MUC16 | MUC16, also named CA125, is overexpressed in ovarian cancer and is regarded as an attractive target for therapy. | Anti-MUC16 CAR-T |
Product Description |
Creative Biolabs is committed to cancer study using multiple advanced technologies and methods, and we provide a system of cancer organoid models to accelerate targeted cell therapy development for solid tumors. Please contact us for further discussion.
Reference
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