New research reveals pathways for aggressive prostate cancer subtype

Cribriform prostate cancer is an aggressive subtype of the disease characterized by its histology, but little is known about its molecular pathways. Research from Vanderbilt-Ingram Cancer Center has revealed new information about these pathways, including potential therapies.

The findings, which are the result of single-cell RNA-sequencing, were published Oct. 13 in Nature Communications. The research was conducted in the lab of Paula Hurley, PhD, associate professor of Medicine and Urology.

The researchers observed an interplay between the inherent properties of cancer cells and microenvironmental factors that contribute to this aggressive subtype of prostate cancer.

The upregulation of MYC-induced genes as well as the role of the NF kappa B gene via the TNF alpha signaling pathway were associated with cribriform prostate cancer. Several molecules were also observed, including some that have implications for therapeutic opportunities.

Men who have cribriform morphology detected after prostate surgery are more likely to experience metastatic recurrence and mortality, so precision therapies are needed.

“Our goal was to identify dysregulated factors associated with cribriform prostate cancer that likely contribute to its aggressive nature and could potentially serve as therapeutic targets,” said Hurley, the study’s corresponding author.

The researchers performed single-cell RNA-sequencing on prostate tissue with cribriform morphologies donated by seven patients. One of the molecules associated with the aggressive subtype included PSMA/FOLH1. Radionuclide therapies that utilize a small molecule targeting PSMA have been shown to have clinical benefit in numerous clinical trials for metastatic castration-resistant prostate cancer. PluvictoTM now has FDA approval for advanced prostate cancer and is being offered at Vanderbilt. A variety of other PSMA-directed therapies are evolving and show promise; an exciting study working to explore radioligands earlier in prostate cancer is currently enrolling patients at Vanderbilt. The in-depth understanding of this aggressive subtype also suggests other classes of therapy, now being studied in clinical trials, could be useful in targeting molecules expressed in cribriform prostate cancer.

“Our study offers molecular and cellular insights into this aggressive subtype of prostate cancer, which we hope will ultimately impact patient care,” said the study’s lead author, Hong Yuen Wong, PhD, research assistant professor of Medicine.

Other Vanderbilt authors included Quanhu Sheng, PhD, Amanda Hesterberg, Sarah Croessmann, PhD, Brenda Rios, Khem Giri, PhD, Jorgen Jackson, Adam Miranda, Evan Watkins, Kerry Schaffer, MD, Meredith Donahue, APRN-BC, Elizabeth Winkler, APRN-BC, David Penson, MD, MPH, MMHC, Joseph A. Smith, MD, S. Duke Herrell III, MD, Amy Luckenbaugh, MD, Daniel Barocas, MD, MPH, Young Kim, MD, PhD, Diana Graves, Giovanna Giannico, MD, Jeffrey Rathmell, PhD, Ben Ho Park, MD, PhD, and Jennifer Gordetsky, MD.

The research received support from the American Cancer Society, the National Cancer Institute, the Ray & Kay Eckstein Charitable Trust, James Rowen, The Breast Cancer Research Foundation, Susan G. Komen, The Canney Foundation, SAGE patient advocates, the Marcie and Ellen Foundation, Amy and Barry Baker, Nashville Wine Auction and the Parker Foundation.