New research from Roswell Park identifies this transcription factor as a tumor suppressor in melanoma
- FOXQ1 gene has been shown to promote development of some carcinomas
- Same gene suppresses melanoma progression, Roswell Park team reports
- Ongoing work seeks to better understand consequences of targeted chemotherapy
BUFFALO, N.Y. — A treatment that works well for one cancer type can possibly make other cancers grow more quickly. That is the striking implication of new research from a team at Roswell Park Comprehensive Cancer Center, published in the journal Cell Reports.
The transcription factor FOXQ1 is a known oncogene that has been previously associated with carcinomas, including many types of breast, colorectal, liver and ovarian cancers. Looking to better understand how this protein might be involved in additional cancer types, a team led by Mikhail Nikiforov, PhD, investigated FOXQ1’s role in melanoma, a distinct cancer type that originates from different types of cells than carcinomas.
What they found — that FOXQ1 suppresses the growth of melanoma cells — was quite unexpected.
“The most surprising finding from this work is that FOXQ1 suppresses exactly the same gene and processes in melanoma cells that it induces in carcinomas,” says Dr. Nikiforov, a Professor of Oncology in the Department of Cell Stress Biology at Roswell Park. “I’ve never come across such a dramatic split in how cancer cells can respond to a single gene. The possible implications for cancer management are quite important. These findings may guide us in the future on how we can avoid use of drugs that, while eliminating one type of cancer, may at the same time induce another.”
The team also reports findings about the mechanisms that enable FOXQ1 to inhibit the same processes in melanoma cells that they promote in carcinomas — processes that hinge on a balance between two types of proteins, the β-catenin and TLE family members. When interacting with FOXQ1, these proteins turn it either into a transcriptional activator (in carcinomas) or a repressor (in melanomas). This results in either induction or repression of N-cadherin (the gene CDH2) — a major regulator of tumor invasion and metastasis. “Our hope is that with further study of these interactions, we will be able to exploit this inverse response and better understand how to better control both melanomas and carcinomas,” adds Dr. Nikiforov.
The study, “Melanoma Suppressor Functions of the Carcinoma Oncogene FOXQ1,” is available at cell.com/cell-reports. This research was supported by four grants from the National Cancer Institute (project nos. P30CA16056, R01CA190533, R01CA193981 and R21CA202162).
The mission of Roswell Park Comprehensive Cancer Center is to understand, prevent and cure cancer. Founded in 1898, Roswell Park is one of the first cancer centers in the country to be named a National Cancer Institute-designated comprehensive cancer center and remains the only facility with this designation in Upstate New York. The Institute is a member of the prestigious National Comprehensive Cancer Network, an alliance of the nation’s leading cancer centers; maintains affiliate sites; and is a partner in national and international collaborative programs. For more information, visit www.roswellpark.org, call 1-800-ROSWELL (1-800-767-9355) or email AskRoswell@Roswellpark.org. Follow Roswell Park on Facebook and Twitter.
Annie Deck-Miller, Senior Media Relations Manager