# How Rapid Anticipatory Estrogen Activation of the Unfolded Protein Response Acts as an Authorizing Signal for Estrogen Receptor Action

> **NIH NIH R01** · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · 2020 · $373,843

## Abstract

Estrogens, acting via estrogen receptor α (ERα), were known to regulate gene expression and to activate
signal transduction pathways. We identified a conserved extranuclear pathway by which 17β-estradiol (E2),
acting through ERα, rapidly activates phosphoplipase C γ (PLCγ) leading to production of inositol triphosphate
(IP3). The IP3 binds to and opens endoplasmic reticulum (EnR) IP3 receptors (IP3R) leading to extremely rapid
(<1 min.) efflux of calcium (Ca2+) from the lumen of the EnR into the cell body. Elevated intracellular Ca2+
primes cells for subsequent actions of E2-ERα; depletion of EnR Ca2+ activates the unfolded protein response
(UPR), inducing the important chaperone BiP/GRP78 (glucose regulated protein 78 kDa). Activation of this
pathway is required for E2-ERα-regulated gene expression, induction of cell proliferation and protects cells
against stress. We target this pathway with our medically promising ERα biomodulator, BHPI, which uses the
same pathway as E2, but induces toxic hyperactivation of the UPR. Our hypothesis is that the products of
activation of this newly unveiled pathway, elevated intracellular calcium (Aim 1), and at later times, BiP
chaperone (Aim 2), link to and regulate subsequent E2-ERα-regulated gene expression and stabilize ERα,
influencing drug resistance and genomic actions of ERα. Our goals are to identify the mechanism(s) by which
these products couple to, and control, gene expression (Aim 1), ERα stability and response to drugs (Aim 2),
and to identify the sensors and signals that allow E2-ERα to rapidly initiate the pathway (Aim 3). Aim 1.
Identify the mechanism(s) by which the product of E2-ERα activation of the pathway couples to and
controls E2-ERα-regulated gene expression. Test the data-driven hypothesis that Ca2+ produced by
pathway activation acts through the Ca2+ sensor calmodulin (CaM) to regulate nuclear E2-ERα:CaM
interaction, E2-ERα dimerization and nuclear localization and thereby controls E2-ERα-regulated gene
expression. Aim 2. Background: In CRISPR/Cas9 generated cell lines expressing constitutively active ERα
mutants, the UPR is activated and ERα is partially resistant to antagonists. Identify the mechanism by
which UPR activation contributes to drug resistance. Test the hypothesis that drug resistance in these
cells arises in part because ERα, together with progesterone-PR, synergistically activate the UPR, inducing
BiP chaperone, which stabilizes ERα, thereby contributing to drug resistant gene expression. Aim 3. Identify
components of the multiprotein complex by which E2-ERα initiates the pathway. Using an unbiased
CRISPR/Cas9 lethality screen, followed by verification and analysis of multiprotein complexes, we will identify
the activating kinase(s), scaffolding proteins, other components of the complex(es), genes that impact the
pathway and probe ERα interactions in the complex.
These studies will establish the initial events that occur when estrogen contacts a cell and identify new
m...

## Key facts

- **NIH application ID:** 9915884
- **Project number:** 5R01DK071909-13
- **Recipient organization:** UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN
- **Principal Investigator:** DAVID J SHAPIRO
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $373,843
- **Award type:** 5
- **Project period:** 2005-07-15 → 2022-10-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9915884

## Citation

> US National Institutes of Health, RePORTER application 9915884, How Rapid Anticipatory Estrogen Activation of the Unfolded Protein Response Acts as an Authorizing Signal for Estrogen Receptor Action (5R01DK071909-13). Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/grant/nih/9915884. Licensed CC0.

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