Suppression of DKK3 protein thwarts pancreatic tumor progression and prolongs survival

Suppression of DKK3 protein thwarts pancreatic tumor progression and prolongs survival
Depletion of DKK3 in a mouse model of pancreatic cancer reduces proliferating tumor cells and prolongs survival by more than double. Credit: Li ran Zhou, PhD., Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston TX 77030, USA

Researchers at The University of Texas MD Anderson Cancer Center have shed new light on why pancreatic tumors are so resistant to therapy. The answer may lie in treating a protein found in the scar-type tissue called stroma which often surrounds the tumors.

The tumor-associated stroma is comprised mostly of stellate cells (PSCs) and its density and possibly the cells themselves are thought to prevent current treatments from effectively killing the tumor. Dickkopf-3 (DKK3), is produced by the stromal cells but acts on the neighboring to increase their growth, metastasis and resistance to therapy. DKK3 has been identified as a potential target for treatment with a newly developed DKK3-blocking antibody, according to results from a study led by Rosa Hwang, M.D., professor in Surgical Oncology and Breast Surgical Oncology. Findings are published in the Oct. 24 online issue of Science Translational Medicine.

Hwang's lab found DKK3 to be highly expressed in (PDAC), the most common type of pancreatic , and specifically by PSCs rather than cancer cells, and her team discovered different ways to silence DKK3 from acting on cancer cells as well as immune cells in the tumor microenvironment. The researchers developed an antibody to block the DKK3 molecule in mice, which not only inhibited tumor growth but also significantly prolonged life.

"Pancreatic cancer has a dismal prognosis and it is unclear if its stromal infiltrate contributes to its aggressiveness.We demonstrated that DKK3 is produced by PSCs and is present in the majority of human pancreatic cancer," said Hwang. "DKK3 stimulates cancer growth, metastasis, and resistance to chemotherapy and immunotherapy. Targeting DKK3 in a pancreatic cancer mouse model boosted immune cell infiltration and more than doubled survival."

DKK3 expression and effects on pancreatic cancer

Hwang's team examined DKK3 expression in human and found that at least two-thirds of patients had moderate-to-very strong levels of DKK3. Compared to normal controls, DKK3 levels were 4.5 times higher in PDAC.

Due to DKK3's dual effects in promotion of tumor growth and in resistance to therapy, Hwang's results indicate that DKK3 is a therapeutic target as either monotherapy or in combination with immunotherapy or chemotherapy.

"Previous efforts to target stroma were directed at broadly eliminating stromal elements," she said. "Our study shows that a more effective strategy may be to inhibit specific tumor-promoting mechanisms attributed to PSCs, such as DKK3."


Explore further

Identification of a driver of fibrosis in chronic kidney disease

More information: A.R. Zhou el al., "Suppression of stromal-derived Dickkopf-3 (DKK3) inhibits tumor progression and prolongs survival in pancreatic ductal adenocarcinoma," Science Translational Medicine (2018). stm.sciencemag.org/lookup/doi/ … scitranslmed.aat3487
Journal information: Science Translational Medicine

Citation: Suppression of DKK3 protein thwarts pancreatic tumor progression and prolongs survival (2018, October 24) retrieved 23 August 2019 from https://medicalxpress.com/news/2018-10-suppression-dkk3-protein-thwarts-pancreatic.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
89 shares

Feedback to editors

User comments

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more