Investigators have discovered that aberrant activation of a specific oncoprotein drives key tumor promoting changes in the prostate tissue microenvironment during cancer progression, according to a Northwestern Medicine study published in Nature Communications.
The study, co-led by Mindy Graham, PhD, research assistant professor of Urology, could inform new targeted therapeutic strategies for all stages of prostate cancer.
Prostate cancer is second leading cause of death in men in the U.S., and one in eight men will be diagnosed with prostate cancer during their lifetime, according to the American Cancer Society.
Prostate cancer is a heterogenous disease, with various genomic and epigenetic alterations driving cancer development. Despite this heterogeneity, prostate cancer tumors share several molecular and cellular characteristics in common, but how prostate cancer cells mediate these changes over time has remained poorly understood.
In the current study, Graham and colleagues performed single-cell RNA-sequencing analysis and complementary in situ tissue staining, and compared the biology of human prostate cancer tissue samples with mouse models of prostate cancer.
“We were very interested in doing a comparative biology study where we have patient tissues that we could rigorously investigate, but then we could do some informative experimental analysis with an appropriate mouse model,” Graham said.
These analyses revealed every human tumor that was analyzed had aberrant activation of the MYC oncoprotein, which is well-known to be upregulated in prostate cancer, and is a “common denominator” across the tumor samples, despite their molecular and pathological heterogeneity.
“This observation was supported when performing differential gene expression and pathway analysis of the publicly available TCGA dataset of primary prostate cancer,” the authors wrote.
To further confirm their findings, the scientists analyzed mouse models of prostate cancer driven by human MYC and found that the increased MYC activity leads to a cascade of alterations in surrounding healthy cells, causing the tissue to be proinflammatory at the precursor stage and then eventually become immunosuppressive as the cancer progressed.
“What was so fascinating to us is we were seeing convergent changes in the mouse model that we could see in the human data,” Graham said. “People think of prostate cancer as an immunologically cold tumor microenvironment. But at the very beginning, at the earliest stages in the precursor setting, it’s actually very inflammatory, but it’s only until it becomes invasive carcinoma when you see this switch that happens from inflammatory to something that resembles an immunologically cold environment with immunosuppressive cell types.”
According to Graham, the findings may inform the development of new targeted treatment approaches for prostate cancer as well as future research that evaluates these key cell state alterations that occur in prostate cancer and many other invasive cancer types.
“My hypothesis is that the changes that happened in the primary setting with MYC oncogene activation are recapitulated in the metastatic setting,” Graham said. “So, the idea is that although you have a different tumor site, the MYC activation in the cancer cells are still there, and so when they’re establishing themselves in this new metastatic site, the same cell type changes in the primary setting are occurring in the metastatic setting. Those insights then will help us to develop therapies that might not only target the primary but also the metastatic setting.”
Rulin Wang, MD, a research associate at the Johns Hopkins University School of Medicine, was a co-first author of the study. Srinivasan Yegnasubramanian, MD, PhD, professor of Oncology, of Pathology, and of Radiation Oncology and Molecular Radiation Sciences at the Johns Hopkins University School of Medicine, was senior author of the study.
This work was supported by the Prostate Cancer SPORE Career Enhancement Program at the Robert H. Lurie Comprehensive Cancer Center of Northwestern University.
This work was supported in part by National Cancer Institute grants P50CA058236, U01CA196390, P01CA247886, U54CA274370 and P50CA180995, the Department of Defense PCRP grant W81XWH-19-1-0450, the Prostate Cancer Foundation, The Allegheny Health Network Johns Hopkins Pilot Project Grant, The Patrick C. Walsh Fund, The Irving Hansen Foundation, The Commonwealth Foundation, and the Maryland Cigarette Restitution Fund.
