1 |
Incorporate novel approaches to manipulate astrocytes in vitro (i.e., immunopanning) and in vivo (i.e., GEMM). |
2 |
Apply unbiased genomic and proteomic analysis of reactive astrocytes (single cell level and population level) associated with brain metastasis from different primary sources (i.e., lung cancer, breast cancer, melanoma). |
3 |
Comparison of brain metastasis-associated reactive astrocytes with those present in other brain injuries (i.e., primary brain tumors, neurodegenerative disorders, ischemia, traumatic brain injury, autoimmune disorders). |
4 |
Identify and characterize specific subpopulations within brain metastasis-associated reactive astrocytes and evaluate their potential therapeutic implications. |
5 |
Dissect the biology behind antimetastatic and prometastatic reactive astrocytes: Are they different subpopulations? Do they coexist in time? Could prometastatic reactive astrocytes be transformed into antimetastatic astrocytes? |
6 |
Does systemic disease (primary tumor and extracranial metastases) influence the brain microenvironment acting on reactive astrocytes before metastases are established in the brain? |
7 |
Do brain metastasis-associated reactive astrocytes influence systemic disease outside the brain and/or organismal homeostasis as shown in other brain disorders? |
8 |
Could reactive astrocytes associated with brain metastasis be the source of biomarkers for early diagnosis or response to therapy? |