Using loss of heterozygosity of microsatellites to distinguish high-grade dysplastic nodule from early minute hepatocellular carcinoma

BackgroundIt is practical significant to seek new applicable adjuvant diagnostic biomarkers to differentiate high-grade dysplastic nodule (HGDN) from well-differentiated minute hepatocellular carcinoma (w-MHCC) due to their closely overlapping morphology.MethodsIn the present study, by using microdissection-based paraffin-embedded tissues, loss of heterozygosity (LOH) patterns of a panel of 22 microsatellite (MS) markers was examined in 8 HGDN, 14 w-MHCC (≤ 1 cm) and 35 larger HCC (LHCC, > 1 cm).ResultsThe results revealed a stepwise increasing fractional allelic loss from HGDN, w-MHCC and LHCC (0.166 ± 0.141, 0.377 ± 0.198, 0.471 ± 0.264, respectively, P = 0.005). Loci-specific analyses showed that LOH on D4S415 (66.7% vs 0.0%, P = 0.04), D1S507 (50.0% vs 0.0%, P = 0.098), and D9S1752 (50.0% vs 0.0%, P = 0.33) occurred more frequently than 50% in w-MHCC, but not in HGDN. On the other hand, LOH on D17S960, D17S1796 and D9S1749 occurred in HGDN, but not in w-MHCC. When compared with w-MHCC, LHCC had a higher LOH frequency on D17S720 (73.9% vs 36.4%, P = 0.04), D17S960 (68.8% vs 0.0%, P = 0.03) and D17S1796 (81.8% vs 0.0%, P = 0.01).ConclusionsThe present study suggests MS-LOH is a simple and specific assay for routinely diagnostic pathology. We recommend that D4S415, D1S507, D9S1752, D17S960, D17S1796 and D9S1749 can be used as the first-line markers for differential diagnosis between HGDN and w-MHCC, and D9S1748, D17S921 and D17S520 with a LOH frequency of 40%–50% in w-MHCC, but netative in HGDN, can be regarded as the second-line candidate markers.

► LOH pattern was analysed in DN and HCC. ► A stepwise increasing fractional allelic loss from HGDN, MHCC and LHCC. ► MS markers can be adjunct for differential diagnosis between HGDN and MHCC. ► MS-LOH is a simple and specific assay for routinely diagnostic pathology.