A431 Xenograft Model

A431 Xenograft Model by Altogen Labs

A431 xenograft model

Squamous cell carcinoma or epidermoid carcinoma is one of the most prevalent types of skin cancer. It develops from squamous cells and can be triggered by UV exposure. The A431 cell line was isolated from epidermal cells of an 85-year-old female with epidermoid carcinoma. A431 is commonly used for studies of skin cancer as well as for pharmaceutical and biomedical purposes. Targeting agents of the EGFR-related signaling pathway show promising anticancer activities in skin cancer patients. Furthermore, preclinical studies of the combined use of radiotherapy (RT) and EGFR inhibitors indicate that the inhibition of EGFR increases the therapeutic efficacy of fractionated irradiation. A 2015 article by Lim et al. published in Cancer Research and Treatment, evaluated the tumor growth suppression and radiation-sensitizing effects of an exogenous epidermal growth factor (EGF) in the A431 xenograft model in vivo. These findings demonstrate the anti-tumor effect of EGF in vivo and show the potential role of EGF as a radiation sensitizer. The A431 cell line (human squamous carcinoma) is used for creating the CDX (Cell Line Derived Xenograft) A431 xenograft mouse model. This CDX model is a proven model that is sensitive to EGF inhibitor therapeutics.

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Basic study design

  1. All cells are maintained at the exponential growth phase prior to injection.
  2. A431 cells are collected by trypsinization and prepared for injection.  Viable cell counts are then determined using a trypan blue exclusion assay (98% cell viability required). The cell suspension is then adjusted to the appropriate density.
  3. Each of the mice (athymic BALB/c nude) will receive a subcutaneous injection (s.c) in the flank of a hind leg containing one million cells.  The volume of the injection is 100 microliters of the matrigel A431 cell suspension.
  4. Three times weekly, the injection sites are palpated until it is determined that tumors are established. Tumors are measured with digital calipers until they reach the required starting volume.
  5. Animals are randomized into cohorts and the administration of the test compound is performed following the treatment schedule.
  6. Tumors are measured daily, with mouse weights recorded 3 times weekly.
  7. Animals are euthanized as tumor size reaches 2,000 mm2 or at the predetermined size limit.
  8. The necropsy is performed as defined for termination of experiment.
  9. Tumors are excised and weighed.  Tumors are documented by digital imaging.
  10. Standard necropsies are performed to collect tissues for downstream analysis.
  11. All tissues can be stabilized in RNAlater, snap frozen in LN2 or prepared for gene expression analysis.

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A431 Xenograft Model

Xenograft animal models are used to assess the effectiveness of experimental test compounds against specific types of cancer. New medicines are tested on staged tumor growths that have been engrafted via subcutaneous or orthotopic inoculation in an immunocompromised mouse or rat model. All clinically approved anti-cancer agents have been evaluated with conventional preclinical in vivo models. Xenograft studies can be highly complex, starting with the selection of the appropriate animal model, choice of tumorigenic cell line, administration method, dosing, analysis of tumor growth rates and tumor analysis (histology, mRNA and protein expression levels).

Altogen Labs provides an array of laboratory services using over 30 standard Cell Line Derived Xenograft (CDX) models and over 20 PDX models. Researchers investigating the role of specific proteins or gene products in regulating tumor growth can benefit from development of protein overexpression (genetically engineered to ectopically express proteins, tumor suppressors, or oncogenes) and RNAi cell lines with long term gene silencing. Altogen Labs provides quantitative gene expression analysis of mRNA expression (RT-PCR) and protein expression analysis using the WES system (ProteinSimple).

The dosing of the experimental compound of interest is initiated, for a staged study, when the mean tumor size reaches a specified volume (typically 50-100 mm3). In an unstaged study, the dosing of the compound of interest is initiated immediately after xenografting. Mice are dosed once or twice a day for 28 days (or other desired study duration) via the chosen route of administration. Tumor volume (mm3) is calculated via the “(W x W x L) / 2” formula, where W is tumor width and L is tumor length.

Animal handling and maintenance at the Altogen Labs facilities are IACUC-regulated and GLP-compliant. Following acclimation to the vivarium environment, mice are sorted according to body mass. The animals are examined daily for tumor appearance and clinical signs. We provide detailed experimental procedures, health reports and data (all-inclusive report is provided to the client that includes methods, results, discussion and raw data along with statistical analysis). Additional services available include collection of tissue, histology, isolation of total protein or RNA and analysis of gene expression. Our animal facilities have the flexibility to use specialized food or water systems for inducible gene expression systems.

Following options are available for the A431 xenograft model:

  • A431 Tumor Growth Delay (TGD; latency)
  • A431 Tumor Growth Inhibition (TGI)
  • Dosing frequency and duration of dose administration
  • Dosing route (intravenous, intratracheal, continuous infusion, intraperitoneal, intratumoral, oral gavage, topical, intramuscular, subcutaneous, intranasal, using cutting-edge micro-injection techniques and pump-controlled IV injection)
  • A431 tumor immunohistochemistry
  • Alternative cell engraftment sites (orthotopic transplantation, tail vein injection and left ventricular injection for metastasis studies, injection into the mammary fat pad, intraperitoneal injection)
  • Blood chemistry analysis
  • Toxicity and survival (optional: performing a broad health observation program)
  • Gross necropsies and histopathology
  • Positive control group employing cyclophosphamide, at a dosage of 50 mg/kg administered by intramuscular injection to the control group daily for the study duration
  • Lipid distribution and metabolic assays
  • Imaging studies: Fluorescence-based whole body imaging, MRI

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A431 Xenograft Model