Head and neck tumor stained for markers of cancer (brown) and p-EMT transition (red), demonstrating cells having undergone a unique transition at the tumor’s outer edge.
Image: Mass. Eye and Ear and Mass General
Mapping Terra Incognita
Researchers have compiled the first atlas of invasive head and neck tumor cells
By Suzanne Dayn
Head and neck tumors that contain cells undergoing a transition from neatly organized blocks into irregular structures pushing out into the surrounding environment are more likely to invade and spread to other parts of the body, according to a new study led by Harvard Medical School researchers from Massachusetts Eye and Ear, Massachusetts General Hospital and the Broad Institute of MIT and Harvard.
The findings, published online Nov. 30 in Cell, provide important clues into how head and neck cancers metastasize and may have implications for other common cancers as well.
As part of the study, the researchers have compiled the first atlas of head and neck cancer, revealing the many different kinds of cells, cancerous and non-cancerous, in primary head and neck tumors and their metastases.
Using a process known as single-cell RNA-sequencing, the researchers analyzed more than 6,000 individual cells from head and neck squamous cell carcinomas—the most common head and neck tumor. Through their analysis, the research team created an atlas of all the different cells present in head and neck cancer. They were also able to characterize a unique structural transition involving cancer cells and normal cells in their environment that allows tumors to spread.
“This is the clearest picture we’ve had of this kind of structural transition in a human tumor,” said co-senior author Bradley Bernstein, HMS professor of pathology at Mass General and an institute member at the Broad. “For years, it’s been known that cells can lose their connections to the surrounding tissue and become more mobile, but when, how and where this occurs in human cancer has been long debated.”
The tell-tale cellular changes described in the study bear the hallmarks of a process known as partial epithelial-to-mesenchymal transition, which causes cells that are ordinarily static to become mobile. The new findings suggest that head and neck tumors temporarily “borrow” this process used in normal embryonic development to invade nearby tissues and spread, and these findings could extend to similar cancers such as breast, prostate and lung cancers.
“While we were excited to provide a rich, detailed description of the genes in every cell type in head and neck tumors, we quickly realized there were unique cancer cells in some patients but not in others,” said co-lead author Sidharth Puram, HMS clinical fellow in otolaryngology and a chief resident in otolaryngology at Mass. Eye and Ear. “We wondered whether these cells could explain why some tumors spread to the neck and beyond, while others do not.”
Head and neck tumors are common in the United States and worldwide, representing the sixth leading cause of cancer-related illness and death. Although these tumors are often found in the tongue, cheek or throat, making them accessible to surgery, they can spread further through the lymph nodes. Unfortunately, once the cancer spreads in this manner, through a process called metastasis, treatment becomes more challenging and patients often have poor outcomes.
Clinicians treating head and neck cancer have faced the daunting possibility of tumor spread for years, with surgeons remaining unsure how to look for metastasis and how to decide whether lymph node tissues in the neck need to be removed. Understanding this process could avoid unnecessary surgery, which carries risks to nerves of the head and neck, and could also aid in planning chemotherapy and radiation treatment.
The researchers envision a future in which identifying tumors undergoing this transition may influence the way that cancer patients are clinically managed. Such knowledge would allow surgeons to make decisions based on the biology of each patient’s tumor, rather than the tumor’s size, and to predict its likelihood of spreading to other parts of the body.
“We may be able to predict with better accuracy than our current staging system which patients will have a poorer prognosis,” said co-senior author Derrick Lin, the HMS Daniel Miller Associate Professor of Otolaryngology and director of Head and Neck Surgical Oncology at Mass. Eye and Ear. “Predicting which patients will develop lymph node metastasis can better inform our treatment strategies. This insight could also lead to the development of new therapies that target this process and prevent metastasis beyond the primary site. Because metastasis is one of the hardest problems to treat and one of the biggest reasons cancer patients do not survive, these findings open up a whole new area of research for the field.”
In addition to Bernstein, Puram and Lin, authors on the Cell study include co-corresponding author Aviv Regev of the Broad and two co-first authors Anuraag Parikh of HMS and Mass. Eye and Ear and Itay Tirosh of the Broad. Additional co-authors from HMS are William Faquin of HMS and Mass General and Mark Varvares of HMS and Mass. Eye and Ear.
Adapated from a Mass. Eye and Ear/Mass General joint news release.
source: Harvard University – Harvard Medical School