Regulation of ER-beta Signaling in Carcinogenesis

University Of Texas Hlth Science Center, San Antonio TX

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Abstract

Estrogen receptor (ER)? exhibits an antitumor activity in multiple cancer types in both tumor-intrinsic and -extrinsic manners. However, little is known as to how such activity can be harnessed with high efficacy and precision, nor is it clear which host cell type(s) mediates the tumor-extrinsic function of ER?. These major knowledge gaps hamper efforts to unleash ER? antitumor activity for cancer therapies. We recently discovered a phosphotyrosine-dependent signaling axis that controls ER? antitumor activity. Furthermore, using a novel knockin mouse model, we found that this phosphotyrosine switch plays a significant role in host cells to promote antitumor immunity. Our central hypothesis is that this ER?-centered signaling axis provides a previously unrecognized molecular handle for mobilizing tumor-extrinsic antitumor activity of ER? in immune cells. Armed with genetic and pharmacological tools that both specifically target this signaling circuit, our multi-PI team will validate this novel hypothesis through three Specific Aims. First, we will identify the exact immune cell type(s) that mediates tumor-extrinsic ER? signaling in antitumor immunity (Aim 1). We will then delineate the upstream regulators and downstream target genes of ER? signaling in immune cells (Aim 2). Lastly, we will assess the anticancer therapeutic potential of targeting this ER? signaling axis to boost current cancer immunotherapies. Findings from these experiments will shed light on a previously under-appreciated signaling pathway governing tumor-immune cell interactions in the tumor microenvironment. As immunotherapies are becoming an important pillar of cancer therapy, the proposed study will help improve clinical outcomes and efficacy of immunotherapy for larger numbers of cancer patients.