Researchers uncover a potential genetic marker associated with better survival outcomes in patients with head and neck cancer

Protein associated with a neurodegenerative disorder may also play a role in preventing the spread of cancer
throat tumor illustration
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3 min read

FINDINGS

Researchers from the UCLA Health Jonsson Comprehensive Cancer Center show for the first time that a gene usually linked to giant axonal neuropathy, a rare and severe neurological condition, also plays a role in inhibiting aggressive tumor cell growth in head and neck cancers.

The team found when the specific genetic variant (GAN gene exon 8 SNP T allele) of the GAN gene isn't present, it leads to the production of certain proteins that make cancer cells more likely to spread and become resistant to treatment.

These findings suggest that the presence of the genetic variant and higher expression of the GAN gene product gigaxonin may contribute to better survival in head and neck cancers and could potentially be used as diagnostic markers for identifying less aggressive forms of the disease.

BACKGROUND

There are multiple neurodegenerative diseases that are associated with an increased risk of cancer. This increased risk is often associated with gene mutations that hinder the cell's ability to repair DNA damage properly. Giant axonal neuropathy, a rare genetic disorder that leads to progressive damage to the peripheral nerves and central nervous system, is caused by mutations in the GAN gene, resulting in loss of expression of the protein called gigaxonin. This protein is crucial for maintaining the structural integrity of cells. In previous studies related to head and neck cancer, the UCLA team found that gigaxonin interacts with another protein called p16 to add a molecule called ubiquitin to a protein called NF-κB. This process, known as ubiquitination, is a way cells regulate the activity of proteins. However, the exact role of gigaxonin in cancer has not yet been well understood. Here, authors show that ubiquitination of NF-κB results in downregulation of Snail, a protein associated with epithelial to mesenchymal transition (EMT), also known as metastasis. Thus, expression of gigaxonin suppresses aggressive growth of human cancer cells.

METHOD

To gain insight into the role of gigaxonin in tumor development, investigators analyzed normal and tumor DNA from cervical and head and neck cancers. They also examined cancer cell lines with different genetic variations to understand the relationship between the genetic variation, gigaxonin expression, and the growth of cancer cells, including their response to cisplatin, a type of chemotherapy. Additionally, they investigated how gigaxonin is involved in ubiquitinating a transcription factor NF-κB and possibly associated with the development of head and neck cancer.

IMPACT

The study provides insights into the molecular mechanisms underlying head and neck cancer progression. If validated in additional studies, the use of gigaxonin as a diagnostic marker could help lead to the development of targeted therapies based on the gigaxonin pathway.

JOURNAL

The study was published in Cancer Research Communications, a journal of the American Association for Cancer Research.

AUTHORS

The co-senior authors are Eri Srivatsan, a professor of surgery at the Veterans Affairs Greater Los Angeles Healthcare System (VA GLAHS) Medical Center and the David Geffen School of Medicine at UCLA, and Dr. Daniel Shin, an assistant professor of medicine at the VA GLAHS Medical Center, and David Geffen School of Medicine. Both are members of the UCLA Health Jonsson Comprehensive Cancer Center and Molecular Biology Institute. The study’s first author is Mysore Veena, a scientist at the Geffen School of Medicine.  Other UCLA authors include Jungmo Gahng, Dr. Mustafa Alani, Albert Ko, Saroj Basak, Isabelle Liu, Kimberly Hwang, Jenna Chatoff, Natarajan Venkatesan, Marco Morselli, Weihong Yan, Ibraheem Ali, Karolina Elżbieta Kaczor-Urbanowicz, Bhavani Shankara Gowda, Patrick Frost, Matteo Pellegrini, Dr. Neda Moatamed and Dr. Marilene Wang.

FUNDING

This work was supported in part by the VA GLAHS, West Los Angeles Surgical Education Research Program, and the Conquer Cancer Foundation/American Society of Clinical Oncology.