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Home NEWS Science News Biology

New mechanism fueling brain metastasis discovered at Wistar

Bioengineer by Bioengineer
October 9, 2019
in Biology
Reading Time: 3 mins read
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The pro-metastatic effect of astrocytes is mediated by activation of the PPAR-gamma pathway in invaded cancer cells and uncovers new use for PPAR-gamma antagonists in cancer therapy

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Credit: The Wistar Institute

PHILADELPHIA — (Oct. 9, 2019) — Scientists at The Wistar Institute described a novel mechanism through which astrocytes, the most abundant supporting cells in the brain, also promote cancer cell growth and metastasis in the brain.

According to a study published online in the journal Cancer Discovery, astrocytes provide fatty acids that activate the PPAR-gamma pathway in cancer cells, enhancing their proliferation.

Brain metastasis remains an important contributor to overall cancer mortality in patients with advanced-stage disease, especially lung, breast, colon and kidney carcinoma, and melanoma. Current therapeutic strategies have shown limited efficacy, underscoring the need to expand our knowledge of brain metastasis mechanisms to identify novel therapeutic targets.

“We know that cancer cells take advantage of the interaction with local cells, especially astrocytes, to survive and proliferate in the brain environment,” said Qing Chen, M.D., Ph.D., assistant professor in the Immunology, Microenvironment & Metastasis Program and senior author of the study. “We wanted to understand the nature of this interaction and what exactly astrocytes provide to support metastatic growth.”

Chen and her collaborators focused on clinically relevant mouse models of melanoma brain metastasis and showed that astrocytes promoted cancer cell proliferation. By investigating the molecular mechanisms of this interaction, they found that the peroxisome proliferator-activated receptor-gamma (PPAR-gamma) pathway is activated in cancer cells that possess elevated ability to form brain metastasis, and it is even more active when these cells are co-cultured with astrocytes.

Genetic and pharmacologic blockade of PPAR-gamma signaling resulted in decreased cancer cell growth and a reduced response to astrocyte-induced proliferative effect, establishing the functional relevance of this pathway in brain metastasis.

The brain is the fattiest organ in the body, enriched in polyunsaturated fatty acids that are needed to support its functions. Astrocytes are a major cellular source of fatty acids. The team showed that polyunsaturated fatty acids released by astrocytes activate PPAR-gamma signaling in cancer cells, which in turn results in enhanced proliferation.

“Our data support that brain metastatic cells take advantage of the high fat supply provided by astrocytes as a nutrient source for their metabolism and growth,” said Yongkang Zou, Ph.D., a postdoctoral fellow in the Chen lab and first author of the study.

Importantly, comparing normal skin, benign nevus, primary tumors, extracranial metastasis, and brain metastasis samples from melanoma patients, the team confirmed the highest PPAR-gamma levels in brain metastatic lesion.

Furthermore, treatment of mouse models of melanoma and breast cancer brain metastasis with a PPAR-gamma inhibitor decreased the metastatic burden and was well tolerated.

“Previous studies have indicated a tumor-suppressive function for PPAR-gamma in primary tumors,” said Chen. “Our work suggests that this pathway may play an opposite role in metastatic cells, particularly in the lipid-rich brain environment, and highlights PPAR-gamma as a viable therapeutic target to control brain metastasis.”

###

Co-authors: Andrea Watters, Nan Cheng, Caroline E. Perry, Gretchen M. Alicea, Joshua L.D. Parris, Meenhard Herlyn, Maureen E. Murphy, Zachary T. Schug from Wistar and Ashani T. Weeraratna, formerly at Wistar; Ke Xu from Boston University School of Medicine; Ezra Baraban, Anupma Nayak and Xiaowei Xu from the Perelman School of Medicine of the University of Pennsylvania.

Work supported by: National Institutes of Health (NIH) grant T32 CA009171 and grants from Susan G. Komen (CCR17487999), The Jayne Koskinas Ted Giovanis Foundation for Health and Policy and the V Foundation for Cancer Research. Additional funding was provided by the Ching Jer Chern Memorial Award. Core support for The Wistar Institute was provided by the Cancer Center Support Grant P30CA010815.

Publication information: Polyunsaturated Fatty Acids from Astrocytes Activate PPAR Gamma Signaling in Cancer Cells to Promote Brain Metastasis, Cancer Discovery (2019). Online publication.

The Wistar Institute is an international leader in biomedical research with special expertise in cancer, immunology, infectious disease research, and vaccine development. Founded in 1892 as the first independent nonprofit biomedical research institute in the United States, Wistar has held the prestigious Cancer Center designation from the National Cancer Institute since 1972. The Institute works actively to ensure that research advances move from the laboratory to the clinic as quickly as possible. Wistar’s Business Development team is dedicated to accelerating the translation of Wistar discoveries into innovative medicines and healthcare solutions through licensing, start-ups and creative collaborations. wistar.org.

Media Contact
Darien Sutton
[email protected]
215-898-3988

Original Source

https://wistar.org/news/press-releases/new-mechanism-fueling-brain-metastasis-discovered-wistar

Related Journal Article

http://dx.doi.org/10.1158/2159-8290.CD-19-0270

Tags: Biology
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