DALLAS - July 6, 2020 - UT Southwestern researchers have identified vast webs of small snippets of the genome that interact with each other and with genes to promote prostate cancer. Their findings, published June 22 in the Journal of Clinical Investigation, could lead to new ways to treat the most common type of malignancy in American men other than skin cancer.
Research over the past few decades has shown that genetic mutations trigger and encourage the growth and spread of many cancer types. However, prostate cancers typically have relatively few of these mutations, explains study leader Ram S. Mani, Ph.D., an assistant professor in the departments of pathology and urology at UTSW.
Instead, how prostate cancers regulate gene expression - which genes are turned off and on, and to what extent - tends to go awry. What causes this aberrant gene regulation has been a mystery. Although previous research had identified pieces of DNA throughout the genome that appeared to be connected to prostate cancer, many of these pieces weren't genes, so their role was unclear.
To help answer these questions, Mani and his colleagues focused on genetic enhancers, short pieces of DNA that help encourage genes to make proteins. However, explains Mani, it's not as simple as a one-to-one ratio of enhancer per gene target. One enhancer may target several genes, or multiple enhancers might target a single gene. Additionally, each enhancer could be up to a million base pairs away from its gene target on the same chromosome - a significant distance that makes it difficult to link enhancers with their genes.
To pair enhancers to their gene targets in prostate cancer, Mani and his team used a technique called ChIA-PET, short for chromatin interaction analysis by paired-end tag sequencing. This technique maps associations of particular proteins with DNA throughout the genome.
The researchers used ChIA-PET to find DNA targeted by a protein called RNA polymerase II, looking for differences between benign prostate cells and prostate cancer cells. RNA polymerase II not only binds to genes to start transcription - the process in which cells use the instructions in DNA to make RNA - but also enhancers for these genes. "When this technique identifies a gene, it also identifies all the enhancers that target that gene at the same time," says Mani, a member of UT Southwestern's Harold C. Simmons Comprehensive Cancer Center.
Using sophisticated analytical techniques, the scientists sorted out each of these complicated interactions unique to prostate cancer cells, finding vast hubs of enhancers that interact not just with genes but also with each other. They found that many enhancers interacted with tens of other enhancers or genes. These interactions explain the abnormal expression of several key prostate cancer genes, such as the androgen receptor gene that's over-expressed in many subtypes of prostate cancer and the oncogene MYC, which plays a role in many cancer types. Further investigation identified some "grammar rules" for enhancers in prostate cancer, grouping genes and enhancers into clusters that strictly interact with each other.
Mani notes that finding these hubs of enhancers and their genes also helps explain the long-standing mystery of the short pieces of DNA connected to prostate cancer that are scattered throughout the genome. This new research suggests that many of these pieces are enhancers.
Manipulating the interaction between these enhancers and their gene targets could eventually be used as a strategy to slow or stop prostate cancer spread or potentially prevent it from developing at all, he adds. "These findings open up a whole new field focused on enhancers," he says, "that could lead to novel prostate cancer treatments."
Susmita G. Ramanand and Jiapei Yuan from UTSW, and Yong Chen from UT Dallas are co-first authors in the study. Mani and Michael Zhang (UT Dallas) are the corresponding authors. Other UTSW researchers who contributed to this study include GuemHee Baek, Mohammed Kanchwala, Yunpeng Gao, Adam Aslam, Nida Safdar, Xiaowei Zhan, Ganesh V. Raj, and Chao Xing.
This study was funded by the NIH Pathway to Independence (PI) Award (R00CA160640), the NIH/NCI R01 grant (R01CA245294), the CPRIT Individual
Investigator Research Award (RP190454), the U.S. Department of Defense Prostate
Cancer Research Program (PCRP) - Impact Award (W81XWH-17-1-0675), Kidney
Cancer Specialized Programs of Research Excellence (SPORE) Career Enhancement Program (CEP) award (P50CA196516), and UT Southwestern startup funds.
About UT Southwestern Medical Center
UT Southwestern, one of the premier academic medical centers in the nation, integrates pioneering biomedical research with exceptional clinical care and education. The institution's faculty has received six Nobel Prizes, and includes 24 members of the National Academy of Sciences, 16 members of the National Academy of Medicine, and 13 Howard Hughes Medical Institute Investigators. The full-time faculty of more than 2,500 is responsible for groundbreaking medical advances and is committed to translating science-driven research quickly to new clinical treatments. UT Southwestern physicians provide care in about 80 specialties to more than 105,000 hospitalized patients, nearly 370,000 emergency room cases, and oversee approximately 3 million outpatient visits a year.
Journal of Clinical Investigation