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Table 1 The different models for the evaluation of breast cancer brain metastasis

From: Biological profile of breast cancer brain metastasis

Model

Example

Advantageous

Disadvantageous

Remarks

MDA-MB-231

Subline of MDA-MB-231

Highly metastatic

Capacity of being used in the in vivo studies for understanding brain tropism

Poor representation of tumor heterogeneity

Genetic engineering and does not reflect the primary tumors

Understanding the genes involved in the process of metastasis including COX2 and HBEGF, among others

BT474, SKBR3

HER2-positive

Improving the knowledge towards the breast cancer subtypes participating in brain metastasis

Lack of representation of TNBC brain metastasis

Improving the knowledge towards the HER2-targeted therapy resistance in the brain

4T1-BR5

Murine brain metastasis model

The major advantageous of this model is being immunocompetent providing the insight about immune-tumor interaction

Its murine origin decreases the relevance to human breast cancer

Poor translational application

Understanding the immune-related mechanisms in brain metastasis

SUM149, SUM190

Inflammatory breast cancer-derived lines

Unique properties of inflammatory breast cancer

This is related to the rare subtypes

Poor brain metastasis

Highlighting the mechanisms involved in the aggressiveness and metastasis of TNBC

Xenograft Models

Injection of MDA-MB-231 or BT474 cells

High carcinogenesis

The direct injection to the brain mimics metastasis

Because of immunocompromised hosts, it has poor value in immune system interaction studies

Allowing to understand the BBB-penetrating drugs and certain mechanisms in the metastasis

Patient-Derived Xenografts (PDX)

From human brain metastases

Mimicking the patient tumor and providing the heterogeneity

Low engraftment rates

Poor affordability

Time-consuming

Valuable for the personalized medicine and understanding the patient response to therapeutics

Genetically Engineered Mouse Models

HER2/Neu transgenic models

Reflecting the HER2-driven breast cancer malignancy

Slow progression

It is not suitable for the high-throughput studies

Highlighting the mechanisms of HER2-positrive breast cancer metastasis to brain tissue

Orthotopic Models

Direct injection into mammary fat pad

Mimicking the primary tumor growth and metastasis

It rarely leads to the brain metastasis without brain-tropic cell lines

Understanding the metastatic cascades and providing tumor microenvironment interactions

  1. Further notes: This table highlights a number of cell lines and animal models for understanding the brain metastasis of breast cancer. The advantageous and disadvantageous of each model have bene provided to further improve the knowledge for the selection of suitable model. Each of these models offers significant benefits for understanding the molecular and cellular mechanisms in the brain metastasis. These models have been advantageous in highlighting the tumor biology, therapy resistance, mechanisms of brain metastasis and providing a platform for testing the novel therapeutic approaches. However, there are still a number of limitations including lack of immune system representation in xenograft models and the complexity of accurately mimicking metastatic processes in vivo. Further information about breast cancer brain metastasis can be found in these references [18,19,20,21]