Alfa Cytology offers a comprehensive in vivo esophageal cancer model development service, designed to accelerate the discovery and validation of novel therapeutics. Leveraging an extensive portfolio of xenograft and patient-derived xenograft (PDX) models, our platform provides robust, clinically relevant systems for preclinical efficacy testing, mechanistic studies, and biomarker evaluation in esophageal cancer research.
Esophageal cancer remains a formidable clinical challenge worldwide, with limited therapeutic options and poor prognosis for many patients. Translational research relies heavily on animal models that faithfully recapitulate the complexity and heterogeneity of human esophageal tumors. At Alfa Cytology, we utilize immunodeficient mouse strains—such as Balb/c nude, CD-1 nude, NOG, NSG, and SCID mice—as hosts for human tumor xenografts. These models enable the engraftment and growth of both established cell lines (e.g., ECA109, OE19, TE5, YES2, TT) and primary patient-derived tumor samples, allowing for the investigation of tumor biology, drug responses, resistance mechanisms, and immunological interactions. Our selection of mouse strains and model subtypes ensures high translational relevance and adaptability to a wide range of research objectives.
Cell line-derived xenograft models are established by subcutaneously or orthotopically implanting cultured human esophageal cancer cell lines (such as ECA109, OE19, TE5, YES2, TT) into immunodeficient mice (e.g., Balb/c nude, CD-1 nude, NSG, SCID). These models offer high reproducibility, rapid tumor growth, and ease of genetic manipulation (e.g., overexpression or knockdown of specific genes, reporter labeling with luciferase or GFP). Key advantages include suitability for high-throughput drug screening, evaluation of genetic and pharmacological interventions, and mechanistic studies of tumor progression and metastasis. Primary applications encompass efficacy testing, dose optimization, and biomarker validation.
PDX models are generated by implanting freshly resected human esophageal tumor tissues directly into immunodeficient mice (e.g., Balb/c nude, NOG, nu/nu). These models preserve the histological architecture, genetic diversity, and tumor microenvironment of the original patient sample, making them highly predictive of clinical outcomes. PDX models are invaluable for evaluating personalized medicine approaches, assessing drug resistance mechanisms, and identifying predictive biomarkers. Their ability to maintain tumor heterogeneity and recapitulate patient-specific responses makes them a gold standard for translational oncology research.
This model category involves the use of human esophageal cancer cell lines that have been genetically engineered (e.g., overexpression or silencing of genes such as SOX9, CPEB4, DOPEY2, TRIM37, PLCE1) or pharmacologically modified (e.g., induction of cisplatin resistance). These cells are then implanted into immunodeficient mice to create models that mimic specific genetic alterations or drug-resistant phenotypes observed in patients. The primary advantages include the ability to dissect molecular pathways, test targeted therapies, and study mechanisms of drug resistance. Applications include target validation, resistance reversal strategies, and pathway-focused drug development.
Alfa Cytology delivers a turnkey solution for esophageal cancer in vivo modeling, encompassing model selection and customization, tumor implantation, drug administration, and comprehensive endpoint analysis. Key efficacy endpoints include tumor volume measurement, growth inhibition rate, survival analysis, metastasis assessment, and imaging-based monitoring (bioluminescence, fluorescence). We offer advanced analytical capabilities such as immunohistochemistry, flow cytometry, molecular profiling (qPCR, Western blot, RNA-seq), and histopathological evaluation. Stringent quality control measures are applied at every stage, including authentication of cell lines and patient samples, health monitoring of animals, and standardized protocols to ensure data reliability and reproducibility.
Partnering with Alfa Cytology provides access to a scientifically rigorous, highly customizable, and fully supported in vivo esophageal cancer modeling platform. Our expert team ensures seamless project execution, timely data delivery, and tailored guidance to accelerate your oncology research and drug development programs. Contact us today to discuss your project requirements and discover how our models can advance your esophageal cancer research objectives.
| Species | Strain | Characteristic (Details) |
|---|---|---|
| Mus musculus (mouse) | Balb/c | Nude; Patient-derived xenograft (Esophagus cancer cells, human) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (CE81T/VGH human esophageal squamous carcinoma cells) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (ECA109 human esophagus cancer cells (SOX9-expressing)) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (ECA109 human esophagus cancer cells (cisplatin-resistant) (CPEB4/DOPEY2-overexpressing)) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (ECA109 human esophagus cancer cells (cisplatin-resistant) (DOPEY2-overexpressing)) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (ECA109 human esophagus cancer cells (cisplatin-resistant) transfected with short hairpin RNA for DOPEY2) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (ECA109 human esophagus cancer cells) |
| Mus musculus (mouse) | Balb/c | Nude; Xenograft (YES2 human esophagus cancer cells) |
| Mus musculus (mouse) | CD-1 | Nude; Xenograft (TE5 human esophagus cancer cells) |
| Mus musculus (mouse) | Crl:SHO-PrkdcscidHrhr | Athymic nude; Xenograft (OE19 human esophagus carcinoma cells) |
| Mus musculus (mouse) | NOG | Patient-derived xenograft (Esophagus squamous carcinoma cells, human) |
| Mus musculus (mouse) | NSG | Immunosuppressed; Xenograft (OE19 human esophagus carcinoma cells (GFP/luciferase expressing)) |
| Mus musculus (mouse) | NSG | Xenograft (Mononuclear cells (blood), human (CD3/CD28-activated)); Xenograft (OE19 human esophagus carcinoma cells) |
| Mus musculus (mouse) | nu/nu | Athymic nude; Xenograft (TT human esophagus cancer cells) |
| Mus musculus (mouse) | nu/nu | Immunosuppressed; Nude; Patient-derived xenograft (Esophagus cancer cells, human) |
| Mus musculus (mouse) | nu/nu | Nude; Xenograft (TT human esophagus cancer cells) |
| Mus musculus (mouse) | Nude; Patient-derived xenograft (Esophagus cancer cells, human (TRIM37/luciferase-expressing)) | |
| Mus musculus (mouse) | Nude; Patient-derived xenograft (Esophagus cancer cells, human) | |
| Mus musculus (mouse) | Nude; Patient-derived xenograft (Human esophagus cancer cells transfected with small interfering RNA for TRIM37/luciferase) | |
| Mus musculus (mouse) | Nude; Xenograft (ECA109 human esophagus cancer cells transfected with short hairpin RNA for PLCE1/GFP) | |
| Mus musculus (mouse) | Nude; Xenograft (ECA109 human esophagus cancer cells) | |
| Mus musculus (mouse) | Nude; Xenograft (TE1 human esophagus cancer cells) | |
| Mus musculus (mouse) | Nude; Xenograft (TE10 human esophagus cancer cells) | |
| Mus musculus (mouse) | Patient-derived xenograft (Esophagus cancer cells, human (HER2 [ERBB2]-positive)) | |
| Mus musculus (mouse) | Patient-derived xenograft (Esophagus cancer cells, human) | |
| Mus musculus (mouse) | Severe combined immune deficiency (SCID); Xenograft (PT1590 human esophagus adenocarcinoma cells) | |
| Mus musculus (mouse) | Xenograft (OE19 human esophagus carcinoma cells (GLI1-overexpressing)) | |
| Mus musculus (mouse) | Xenograft (OE19 human esophagus carcinoma cells) |
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