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Sphingosine Kinase 1/S1P Axis in Endocrine Resistant Breast Cancer

内分泌耐药乳腺癌中的鞘氨醇激酶 1/S1P 轴

基本信息

批准号：
9519545
负责人：
Melissa Ann Maczis
金额：
$ 3.66万
依托单位：
VIRGINIA COMMONWEALTH UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2017
资助国家：
美国
起止时间：
2017-07-10 至 2020-07-09
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9519545
关键词：
Address Animal Model Binding Breast Cancer Cell Breast Cancer Patient Breast Cancer Treatment Cancer Prognosis Cell Nucleus Cell membrane Cessation of life Clinical Common Neoplasm Cytosol DNA Binding Data Dimerization Disease Distant Metastasis Down-Regulation Endocrine Epidermal Growth Factor Receptor Estradiol Estrogen Receptor alpha Estrogen Receptors Event Experimental Animal Model Foundations GPER gene Gene Expression Gene Targeting Genomics Growth Growth Factor Human In Vitro Ligand Binding Domain Ligands Link MAPK3 gene Malignant Neoplasms Mammary Neoplasms Mediating Membrane Metastatic breast cancer Neoplasm Metastasis Pathologic Pathway interactions Patient-Focused Outcomes Patients Play Production Progesterone Receptors RNA Splicing Recurrence Regulation Research Resistance Role SPHK1 enzyme Severities Signal Pathway Sphingolipids Sphingosine Tamoxifen Testing Therapeutic Tissue Microarray Transactivation Transcriptional Activation Domain Up-Regulation Variant Woman base breast cancer progression cancer cell cancer diagnosis cancer type experimental study hormone therapy improved in vivo Model innovation malignant breast neoplasm mortality neutralizing antibody non-genomic novel outcome forecast receptor response sphingosine 1-phosphate therapy resistant triple-negative invasive breast carcinoma tumor tumor growth

项目摘要

Project Summary Breast cancer is the most commonly diagnosed cancer in women, and more than 40,000 women in the US die each year of metastatic breast cancer. The estrogen receptor-α (ERα) and its ligand 17β-estradiol (E2) play critical roles in breast cancer. E2 promotes breast cancer progression by eliciting genomic effects in ERα- positive breast cancers by binding to its canonical receptor ERα66. However, triple negative breast cancers (TNBC) lack ERα66 and do not respond to hormonal therapy such as tamoxifen. It has been suggested that the novel splice variant ERα36 mediates rapid, non-genomic responses to E2. Previous studies from our lab showed that E2 activates sphingosine kinase 1 (SphK1), which produces the bioactive sphingolipid metabolite sphingosine-1-phophate (S1P). Secreted S1P in turn binds to its receptors leading to downstream signaling pathways and transactivation of EGFR important for breast cancer progression and metastasis. My preliminary results led me to propose the intriguing hypothesis that ERα36 is the membrane receptor required for E2- mediated SphK1 activation and rapid secretion of S1P, which regulates key non-genomic effects of E2 involved in hormone therapy resistance of breast cancer. I also suggest that increased expression of SphK1 and ERα36 play an important role in de novo and acquired endocrine resistance in metastatic breast cancer. Understanding the mechanisms responsible for de novo and acquired hormonal therapy resistance may provide clues to better treatments. The following specific aims will be pursued to test this hypothesis: (1) Establish the E2 receptor involved in activation of the SphK1/S1P axis in TNBC cells; (2) Determine the role of SphK1/S1P axis in in vitro and in vivo models of endocrine resistant breast cancer; (3) Examine the correlation of expression of SphK1 and ERα36 in endocrine resistant metastatic breast cancer patients and prognosis. This proposal will establish the role of the SphK1/S1P axis in non-genomic effects of E2 and in the regulation of endocrine resistance in metastatic breast cancer and will lay the foundation for further research on potential targeting of the SphK1/S1P pathway as an innovative therapeutic option to circumvent endocrine resistance and improve patient outcome.

项目总结