Research Horizons


Scientists Regenerate 3D Skin to Study Cancer-Causing DNA Defects in Kids

Skin Deep

Physicians and scientists at Cincinnati Children’s used new stem cell technology to regenerate and study living patient-specific skin in the lab, giving them a precise view of how inherited DNA defects cause skin damage and deadly squamous cell carcinoma in children and young adults with Fanconi anemia (FA).

Reporting their findings in Cell Stem Cell, the researchers are now using the complex 3D laboratory models of FA patient epidermis – and the enhanced biological detail they provide – to screen for drugs that could slow or stop the disease progression.

Study authors explain that new human stem cell-derived tissue models overcome inherent limitations when studying human disease in mice, giving researchers an innovative tool to finally solve what has been a long-standing and dangerous molecular mystery.

“Squamous cell carcinoma is a global health problem, and DNA instability in children with Fanconi anemia makes them extremely susceptible,” said Susanne Wells, PhD, the study’s principal investigator and a cancer biologist at the Cincinnati Children’s Cancer and Blood Diseases Institute. “Unlike the general population, squamous cell carcinomas that arise in the head, neck, anogenital regions, and skin of children and young adults with FA tend to be unusually aggressive and deadly.”

Treatments are available for FA, but Wells explained that they come with side effects because of how the disease works.

“We need effective treatments, but identifying the molecular and cellular consequences of FA gene mutations has been difficult because mouse models don’t fully recapitulate human disease. Fortunately, our bioengineered models of 3D human epidermis are helping us overcome this,” said Wells, who is also director of the Epithelial Carcinogenesis and Stem Cell Program.

A Pathway to DNA Instability

FA is an inherited disorder caused by loss of function mutations in over 20 genes in human reproductive (germline) cells. Usually, the FA pathway plays an important role in normal skin structure and function. And although all cells contain crosslinked DNA, defective DNA repair machinery in people with FA causes the accumulation of defective crosslinks. This makes kids with FA prone to DNA instability, bone marrow failure, and cancer.

Researchers on the current study demonstrate this important role in their most recent data. They conducted a small controlled clinical test to demonstrate that patients with FA mutations are more prone to skin damage and blistering from environmental stress. The test, approved by the Cincinnati Children’s Institutional Review Board, involved applying moderate pressure to the arms of children and young adults with FA and to a control group without FA.

Individuals with FA developed skin blisters much faster when compared to individuals in the non-FA control group, suggesting intrinsic skin fragility in this population.

Mimicking Nature’s Developmental Process

To track the biological development of epidermal vulnerabilities in children with FA, donated skin tissue was used to generate patient-derived pluripotent stem cells (PSCs). The PSCs take on embryonic-like traits and can form any kind of tissue in the body.

According to the study’s first author, Sonya Ruiz-Torres, PhD, a fellow in the Wells laboratory, the researchers are continuing their project. Because the study was limited by a small number of patients, the researchers are generating 3D human organotypic skin rafts to study a broader range of people with FA mutations. This should give scientists a more comprehensive look at different FA gene mutation disease processes, understand how these promote squamous cell carcinoma, and help advance the potential clinical impact of their work.

–Post written by Barrett Brunsman

Publication Information
Original title: Inherited DNA Repair Defects Disrupt the Structure and Function of Human Skin
Published in: Cell Stem Cell
Publish date: Nov. 23, 2020
Read the Study

Research By

Sonya Ruiz-Torres, PhD
Division of Oncology
Research Fellow
Susanne Wells, PhD
Director, Epithelial Carcinogenesis and Stem Cell Program
The goal of our studies is to advance our understanding of both HPV-related and -unrelated SCC development, and to develop new approaches to the diagnosis and treatment of HPV as a major cause of cancer worldwide.