What Causes Nose Cancer? Risk Factors Explained

Nose cancer refers to a group of malignancies that arise in the nasal cavity (the air passage behind the nose), the paranasal sinuses (air-filled spaces in the surrounding bones), and the nasopharynx (located at the top of the throat). These cancers are rare, accounting for less than 5% of all head and neck tumors annually. Understanding the causes involves looking at a complex interplay of personal habits, environmental triggers, viral infections, and inherited traits.

Primary Lifestyle and Environmental Risk Factors

Inhaling toxic substances over a long period is a major risk factor for cancers in the nasal cavity and sinuses. Tobacco use, particularly cigarette smoking, introduces numerous carcinogens that damage the DNA of the lining cells, often leading to squamous cell carcinoma. The risk increases significantly with the duration and quantity of smoking, and smokeless tobacco products also pose a danger to these tissues.

Occupational exposure to specific dusts and chemicals is another significant environmental factor, often involving a long latency period. Workers in woodworking trades (furniture, cabinetry) face elevated risk due to chronic exposure to hardwood dust. Exposure to leather dust in shoemaking and textile fibers has also been linked to an increased incidence of nasal and sinus adenocarcinoma.

Metals such as nickel compounds and chromium (in mining, refining, and plating) are recognized carcinogens for the nasal lining. Formaldehyde and isopropyl alcohol production processes are also contributing factors. These airborne irritants damage the mucosal lining, initiating a chronic inflammatory process that can result in malignant transformation. Heavy alcohol consumption can act synergistically with smoking to amplify the carcinogenic effect on the upper aerodigestive tract.

Viral and Biological Contributors

Infectious agents play a dominant role in the development of nasopharyngeal cancer (NPC). The Epstein-Barr Virus (EBV), a common human herpesvirus, is closely associated with virtually all cases of undifferentiated NPC worldwide. Although most people are infected with EBV asymptomatically, the virus establishes a latent infection in nasopharyngeal epithelial cells that, combined with other factors, drives tumor formation.

Viral genes, such as LMP1, expressed during this latent phase alter the growth cycle of infected cells, promoting uncontrolled proliferation. Human Papillomavirus (HPV) is another viral agent implicated in a subset of nasal and paranasal sinus cancers, particularly high-risk types like HPV-16. HPV is found in approximately 30% of sinonasal squamous cell carcinomas, where it acts as an oncogenic driver.

Long-term chronic inflammation within the nasal and sinus passages also contributes to cancer risk. Persistent conditions like chronic sinusitis, especially when linked to environmental irritant exposure, create a microenvironment of constant cell turnover. This prolonged irritation increases the opportunity for DNA damage and genetic mutations to accumulate, potentially leading to malignant growth.

Genetic and Unavoidable Risk Factors

Certain factors influencing the risk of nose cancer are intrinsic and cannot be modified. The risk for both sinonasal and nasopharyngeal cancers increases with age, with most diagnoses occurring in people in their 50s and 60s. Males are statistically more likely to be diagnosed than females.

Geographic location and ethnicity are powerful predictors of nasopharyngeal cancer (NPC) incidence. NPC exhibits a unique global distribution, with high prevalence rates observed in specific populations, notably those of Southern Chinese descent, Southeast Asians, and indigenous groups in the Arctic. This disparity suggests a strong underlying genetic susceptibility involving specific variations in the human leukocyte antigen (HLA) genes.

These HLA gene variants may impair the immune system’s ability to clear EBV-infected cells. Having a first-degree relative with NPC slightly increases an individual’s risk, pointing to a familial component. This inherited genetic vulnerability, combined with environmental factors or EBV infection, creates a complex risk profile.