Noninvasive, Low-Cost Test Accurately Diagnoses Oral Cancer in 30 Minutes

The findings of the study by a team of researchers, led by Case Western Reserve University (Cleveland, OH, USA), are based on a novel scoring system that assesses the levels of two proteins in cells collected from suspicious oral lesions in dental or ear, nose, and throat (ENT) clinics. The two proteins in question are human beta defensin 3 (hBD-3), which is highly expressed in early-stage oral cancer, and hBD-2, whose levels remain low or unchanged. The test calculates the beta defensin index (BDI) by comparing the ratio of hBD-3 to hBD-2 at the lesion site against the ratio at a normal site. A BDI above a certain threshold indicates the presence of cancer, while a lower score suggests its absence. The BDI, determined through routine lab procedures, has been independently validated at two different facilities using the same protocols.

This lab-based method could significantly reduce the need for biopsies in primary care clinics by up to 95%, helping clinicians identify patients who genuinely require a biopsy. The test is particularly advantageous in developing countries, where oral cancer is prevalent and pathology services are often inadequate or non-existent. Additionally, the positive outcomes from this lab-based approach have led to the creation of a point-of-care (POC) device. This innovative POC diagnostic tool, which measures the protein ratio, can be used directly in clinics and deliver results in about 30 minutes.

“When we first discovered hBD-3, we saw it acted as a ‘good guy,’ involved in wound-healing and killing microbes,” said Aaron Weinberg, chair of the Department of Biological Sciences at the Case Western Reserve School of Dental Medicine and the study’s lead researcher. “When we found it was regulated the same way certain cells grow uncontrollably, we started studying hBD-3 in the context of oral cancer.

“Imagine our surprise when this Dr. Jekyll turned out to be Mr. Hyde,” he said. “We found it was not only promoting tumor growth but was overexpressed in the early stages of the disease, while another member, hBD-2, wasn’t changing. This difference in levels of expression of the two proteins compared to the opposite side in the same patient led us to examine the BDI’s ability to distinguish cancer from benign lesions.”

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Case Western Reserve University