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Immunology and Infection
Un modelo ortotópico de cáncer de ovario seroso en ratones inmunocompetentes para In vivo
Un modelo ortotópico de cáncer de ovario seroso en ratones inmunocompetentes para In vivo
JoVE Journal
Immunology and Infection
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JoVE Journal Immunology and Infection
An Orthotopic Model of Serous Ovarian Cancer in Immunocompetent Mice for in vivo Tumor Imaging and Monitoring of Tumor Immune Responses

Un modelo ortotópico de cáncer de ovario seroso en ratones inmunocompetentes para In vivo Imágenes y seguimiento de tumores de las respuestas inmunitarias del tumor

Full Text
18,989 Views
10:35 min
November 28, 2010

DOI: 10.3791/2146-v

Selene Nunez-Cruz1, Denise C. Connolly2, Nathalie Scholler1

1Penn Ovarian Cancer Research Center, Center for Research on Reproduction and Womans Health, Department of Obstetrics and Gynecology,University of Pennsylvania-School of Medicine, 2Women's Cancer Program,Fox Chase Cancer Center

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This study utilizes a syngeneic mouse model of serous ovarian cancer to investigate tumor growth and the tumor microenvironment. The model allows for in vivo imaging of tumor progression, providing insights into ovarian cancer development.

Key Study Components

Area of Science

  • Ovarian cancer research
  • In vivo imaging techniques
  • Tumor microenvironment analysis

Background

  • Ovarian cancer is often diagnosed at advanced stages.
  • It is the most lethal gynecologic malignancy in the U.S.
  • Understanding tumor growth dynamics is crucial for developing treatments.
  • Mouse models provide a platform for studying cancer biology.

Purpose of Study

  • To develop a model for studying serous ovarian cancer.
  • To enable in vivo imaging of tumor progression.
  • To investigate the tumor microenvironment in a controlled setting.

Methods Used

  • Transduction of MOV1 cell line with Katushka fluorescent protein.
  • Orthotopic implantation of tumor cells into the ovary of transgenic mice.
  • Monitoring tumor growth through in vivo imaging techniques.
  • Utilization of immunocompetent mouse models for accurate representation.

Main Results

  • Successful implantation of MOV1 KAT cells in the ovarian tissue.
  • Effective in vivo imaging demonstrated tumor progression.
  • Insights into the tumor microenvironment were obtained.
  • The model can be used for further studies on ovarian cancer.

Conclusions

  • The syngeneic mouse model is a valuable tool for ovarian cancer research.
  • In vivo imaging provides real-time insights into tumor dynamics.
  • Future studies can leverage this model for therapeutic developments.

Frequently Asked Questions

What is the significance of using a syngeneic mouse model?
Syngeneic mouse models allow for the study of tumor growth in an immunocompetent environment, closely mimicking human cancer biology.
How does in vivo imaging contribute to cancer research?
In vivo imaging enables researchers to monitor tumor progression and response to treatments in real-time, providing critical data for understanding cancer dynamics.
What are the advantages of using fluorescent proteins in tumor studies?
Fluorescent proteins allow for the visualization of tumors in live animals, facilitating the study of tumor behavior and interactions with the microenvironment.
Why is ovarian cancer particularly challenging to treat?
Ovarian cancer is often diagnosed at advanced stages, making it more difficult to treat effectively due to the spread of the disease.
What future research could be conducted using this model?
Future research could explore therapeutic interventions, the effects of different treatments, and the role of the tumor microenvironment in cancer progression.

Para el estudio de

El cáncer de ovario generalmente se diagnostica en una etapa avanzada, cuando la proporción de casos por letalidad es alta. Por lo tanto, el cáncer de ovario sigue siendo la más letal de todas las neoplasias malignas ginecológicas entre las mujeres en los Estados Unidos. En este trabajo describimos un modelo murino singénico de cáncer de ovario seroso que permite, tanto la obtención de imágenes in vivo como el estudio del microambiente tumoral.

Transducimos de manera estable con la proteína fluorescente kaka derivada de C nmy y la línea celular de cáncer de ovario derivada de un ratón transgénico DR 26 para MIS dos etiquetas R. Estas células, llamadas MOV one cat, se inyectan en el ovario de un ratón transgénico no propenso a tumores, TG MIS, dos marcas R, para que crezca y se convierta en un cáncer de ovario seroso fluorescente. Las imágenes in vivo se realizan para controlar la progresión del tumor.

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