Sun Won Hong
Yonsei University · Medicine
About the Lab
Professor Sun Won Hong's research lab specializes in diagnostic and molecular pathology, with a focus on thyroid and salivary gland cancers. The lab investigates the immunohistochemical and clinicopathological features of rare and aggressive thyroid carcinoma variants, such as the diffuse sclerosing variant of papillary thyroid carcinoma (DSVPC), aiming to improve diagnostic accuracy and classification. Additional research explores tumor microenvironment interactions, including eosinophil recruitment in gastric carcinoma and bacterial metabolism of furfural derivatives, highlighting a multidisciplinary approach to cancer biomarkers and pathogenesis. The lab also contributes to the development of reliable classification systems for salivary gland lesions based on molecular and clinical outcomes.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15DSVPC is a major subtype of PTC in the young.
Diffuse sclerosing variant of papillary carcinoma (DSVPC) is a rare variant of papillary thyroid carcinoma (PTC). It shows different clinicopathologic features to the conventional PTC, but the immunohistochemical characteristics of DSVPC are yet to be more clearly defined. The purpose of this study was to investigate the immunohistochemical features of DSVPC, which are different from those of PTC. Tissue microarray was constructed from the paraffin-embedded tissue of 49 DSVPC and 50 conventional
Abstract The Furfural and 2-furoic acid present in bacterial cultures were extracted and detected by High pressure Liquid Chromatogrphy (HPLC). Using the methanol/water solvent (70/30), the column, μ Bondapak C18 (Waters Associates) seperated these compounds well. The detection was performed at 254 nm where binary mixtures were absorbed. This method provided a rapid and simultaneous detection for the conversion of furfural into 2-furoic acid followed by the utilization of 2-furoic acid during ba
The newly proposed MSRSGC appears to be a reliable system for classification of salivary gland lesions according to the associated ROM.
We have occasionally experienced eosinophilic abscess of the liver in patients with gastric carcinoma, suggesting that some eosinophil mobilizing (chemotactic and proliferative) factors might be produced by carcinoma cells. The aim of this study was to determine whether or not gastric carcinoma expresses the well-known eosinophil chemotactic factors (ECFs) and whether or not the expression is related to the histologic subtypes. Seventeen consecutive surgically removed tumor-bearing stomachs were
Using CD56 alone showed relatively low specificity despite high sensitivity for detecting malignancy. Combining CD56 with HBME-1 could increase the specificity. Thus, we suggest that CD56 could be a useful preoperative marker for differential diagnosis of TBSRTC category III samples.
Recently, the rearrangement of RET proto-oncogene has been reported to be the most common genetic change in papillary thyroid carcinoma (PTC). However, its prevalence has been reported variably and its relation to clinical outcome has been controversial. The characteristic nuclear features of PTC usually render the diagnosis, but problem arises with equivocal cytologic features that are present focally. Although there remains some controversy, CK19 has been reported to be a useful ancillary tool
Aflatoxin B1 (AFB1), a fungal toxin produced by Aspergillus flavus, is known to be a possible hepatocarcinogen. But the molecular biologic changes which may occur following exposure to AFB1 are not known and thus the carcinogenesis is not yet understood. This study was performed to examine the expressions of c-myc, c-fos and TGF-alpha genes and to investigate the possible role of those molecular biologic changes in hepatic regeneration and in the development of hepatocellular carcinoma (HCC). Sp
These results indicate that mixed Th1 (TNF-α, IFN-γ , and IL-2) and Th2 (IL-10) immunity might play a role in the antitumor effect in terms of lymph node metastasis.
Although active inflammation may be deleterious and indicate immunologic activation in chronically rejected grafts, the underlying mechanism of tissue destruction has been little studied. Twenty-four cases of chronic rejection (CR) with or without acute rejection (AR) were stained with antibodies against CD3, CD8, CD68, granzyme B and TIA-1, and the number of positive cells were counted. Eleven cases of AR served as controls. The number of CD3 and CD8 positive cells increased in the acute on CR
Research Areas
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