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Diana M Cittelly

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Associate Professor

University of Colorado Anschutz Medical Campus
Country flagUnited States

Research Interests

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About

Diana M Cittelly is an Associate Professor at the University of Colorado Anschutz Medical Campus in the United States. Her research focuses on the mechanisms of brain metastases, particularly in breast cancer, and the impact of sex steroid hormones on brain tumor progression. She has contributed to global interdisciplinary collaborations aimed at improving patient outcomes for brain metastases and has published recent studies on radiation-induced cytotoxic edema.

Recent Grants

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Mechanisms underlying pro-metastatic effects of estrogen in the brain niche

Open Date: 2018-04-01

Close Date: 2023-03-31

Grant: Close

Role of IL13RA2 as a Functional Biomarker in Breast Cancer Brain Metastasis

Open Date: 2013-10-01

Close Date: 2014-09-01

Grant: Close

Hormonal regulation of the brain microenvironment and its contribution to brain m

Open Date: 2013-09-29

Close Date: 2017-08-31

Grant: Close

Contribution of Progesterone-Regulated miRNAs to the Expansion of an Aggressive Stem Cell-Like Population in Luminal Breast Cancer

Open Date: 2009-10-01

Close Date: 2010-09-01

Grant: Close

Altered MicroRNA Activity Promotes Resistance to Endocrine Therapy

Open Date: 2006-10-01

Close Date: 2007-09-01

Articles (5)

Year:

2026

Year:

2025

Year:

2025

Background Brain edema is a common complication of brain metastases (BM) and associated treatment. The extent to which cytotoxic edema, the first step in the sequence that leads to ionic edema, vasogenic edema, and brain swelling, contributes to radiation-induced brain edema during BM remains unknown. This study aimed to determine whether radiation-associated treatment of BM induces cytotoxic edema and the consequences of blocking the edema in preclinical models of breast-cancer brain metastases (BCBM). Methods Using in vitro and in vivo models, we measured astrocytic swelling, trans-electric resistance (TEER), and aquaporin 4 (AQP4) expression following radiation. Genetic and pharmacological inhibition of AQP4 in astrocytes and cancer cells was used to assess the role of AQP4 in astrocytic swelling and brain water intake. An anti-epileptic drug that blocks AQP4 function (topiramate) was used to prevent cytotoxic edema in models of BM. Results Radiation-induced astrocytic swelling and transient upregulation of AQP4 occurred within the first 24 hours following radiation. Topiramate decreased radiation-induced astrocytic swelling and loss of TEER in astrocytes in vitro, and acute short-term treatment (but not continuous administration), prevented radiation-induced increase in brain water content without pro-tumorigenic effects in multiple preclinical models of BCBM. AQP4 was expressed in clinical BM and breast-cancer cell lines, but AQP4 targeting had limited direct pro-tumorigenic or radioprotective effects in cancer cells that could impact its clinical translation. Conclusions Patients with BM could find additional benefits from acute and temporary preventive treatment of radiation-induced cytotoxic edema using anti-epileptic drugs able to block AQP4 function.

Year:

2023

Year:

2022

Collaborators (3)

scott floyd

Associate Professor

Duke University

UNITED STATES
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Manmeet Singh Ahluwalia

Professor of Translational Medicine

Florida International University Herbert Wertheim College of Medicine

UNITED STATES
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J. Neman

-

UNITED STATES
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