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논문 기본 정보

자료유형
학술저널
저자정보
Yun Kyung Jung (Hanyang University College of Medicine) Kiseok Jang (Hanyang University College of Medicine) Seung Sam Paik (Hanyang University College of Medicine) Yong Jin Kwon (Hallym University Kangnam Sacred Heart Hospital) Han Jun Kim (Hanyang University College of Medicine) Kyeong Geun Lee (Hanyang University College of Medicine) Hwon Kyum Park (Hanyang University College of Medicine) Dongho Choi (Hanyang University College of Medicine)
저널정보
대한외과학회 Annals of Surgical Treatment and Research Annals of Surgical Treatment and Research Vol.91 No.1
발행연도
2016.6
수록면
23 - 28 (6page)

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Purpose: Previous studies have shown the role of Sal-like protein 4 (SALL4) as a biomarker in hepatocellular carcinoma (HCC), and some studies have shown the relationship between SALL4 and prognosis. Given the debates in study groups differences in terms of etiologic causes between Western and Asian HCC and detection methods, we attempted to verify the features of SALL4 immunoreactivity and its clinical correlation in Korean HCC patients.
Methods: Immunohistochemical staining of SALL4 of tissue microarrays (TMAs) consisting of 213 surgically resected HCC patients’ tissue were scored in a semiquantitative scoring system with immunoreactive score and the results analyzed with clinical outcome, in addition to general demographics and clinical characteristics.
Results: SALL4 immunoreactivity was expressed in 50 cases. Relevance between SALL4 and α-FP correlated significantly (P= 0.002). Also, the SALL4-positive patients had considerably higher tumor grade (P < 0.001). The survival analysis showed negative correlation with SALL4 immunoreactivity in all HCC patient groups, but SALL4 immunoreactivity in T3 and T4 HCC correlated with poor prognosis.
Conclusion: Here, we found that positive immunostaining of SALL4 is correlated with poor patient survival outcome in large and undifferentiated Korean HCC. SALL4 expression showed close relationship with clinical outcomes of HCCs in Korean patients.

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UCI(KEPA) : I410-ECN-0101-2017-514-001019605