Literature DB >> 23347651

Immunohistochemical expression of SALL4 in hepatocellular carcinoma, a potential pitfall in the differential diagnosis of yolk sac tumors.

Nilda Gonzalez-Roibon1, Betina Katz, Alcides Chaux, Rajni Sharma, Enrico Munari, Sheila F Faraj, Peter B Illei, Michael Torbenson, George J Netto.   

Abstract

SALL4 is a transcription factor that serves as a marker of yolk sac tumor. Yolk sac tumor and hepatocellular carcinoma share histologic, serologic, and immunohistochemical features. Previous studies have shown lack of SALL4 expression in hepatocellular carcinoma, suggesting utility in this differential diagnosis. Sixty-nine samples of hepatocellular carcinoma were retrieved from surgical pathology archives and used to construct 9 tissue microarrays. A germ cell tumor tissue microarray containing 10 yolk sac tumors was used for comparison. Extent, intensity, and pattern of nuclear SALL4 expression were assessed in each spot. Mean percentage of expression was calculated for each tumor and used during analysis. Optimal discriminatory extent of expression cutoff was determined by receiver operating characteristic curve analysis. Other potential discriminatory markers including Hep Par1 were also evaluated. Forty-six percent (32/69) of hepatocellular carcinoma and all yolk sac tumors revealed at least focal expression of SALL4. A unique punctuate/clumped pattern of nuclear staining was present in 94% (30/32) of hepatocellular carcinoma, whereas all yolk sac tumors displayed a diffuse finely granular nuclear staining pattern. A 25% extent of SALL4 expression cutoff was found to be optimal for the distinction of yolk sac tumor from hepatocellular carcinoma yielding a sensitivity of 100%, specificity of 92.8%, and a positive predictive value of 66.6% for yolk sac tumor diagnosis. The addition of Hep Par1 increased the specificity (99%) and positive predictive value (90%). This is the first report of SALL4 expression in hepatocellular carcinoma. Our finding should be taken into consideration in the differential diagnosis of hepatocellular carcinoma and yolk sac tumor. The unique punctuate/clumped pattern seen in hepatocellular carcinoma cases could be of further discriminatory value.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23347651     DOI: 10.1016/j.humpath.2012.10.017

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  6 in total

1.  SALL4 expression in germ cell and non-germ cell tumors: a systematic immunohistochemical study of 3215 cases.

Authors:  Markku Miettinen; Zengfeng Wang; Peter A McCue; Maarit Sarlomo-Rikala; Janusz Rys; Wojciech Biernat; Jerzy Lasota; Yi-Shan Lee
Journal:  Am J Surg Pathol       Date:  2014-03       Impact factor: 6.394

2.  High-level expression of divergent endodermal lineage markers in gonadal and extra-gonadal yolk sac tumors.

Authors:  Hadi Shojaei; Hong Hong; Raymond W Redline
Journal:  Mod Pathol       Date:  2016-07-22       Impact factor: 7.842

3.  SALL4 Expression in Hepatocellular Carcinomas Is Associated with EpCAM-Positivity and a Poor Prognosis.

Authors:  Hyunjin Park; Hyejung Lee; An Na Seo; Jai Young Cho; Young Rok Choi; Yoo-Seok Yoon; Ho-Seong Han; Young Nyun Park; Haeryoung Kim
Journal:  J Pathol Transl Med       Date:  2015-08-10

4.  Clinicopathologic characteristics of SALL4-immunopositive hepatocellular carcinoma.

Authors:  Junji Shibahara; Sumiyo Ando; Akimasa Hayashi; Yoshihiro Sakamoto; Kiyoshi Hesegawa; Norihiro Kokudo; Masashi Fukayama
Journal:  Springerplus       Date:  2014-12-10

5.  SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma.

Authors:  Gang Deng; Lei Zhu; Feizhou Huang; Wanpin Nie; Wei Huang; Hongbo Xu; Shaopeng Zheng; Zhongjie Yi; Tao Wan
Journal:  Oncotarget       Date:  2015-09-29

6.  Up-Regulation of SALL4 Is Associated With Survival and Progression via Putative WNT Pathway in Gastric Cancer.

Authors:  Yang Yang; Xiaohong Wang; Yiqiang Liu; Ying Hu; Zhongwu Li; Ziyu Li; Zhaode Bu; Xiaojiang Wu; Lianhai Zhang; Jiafu Ji
Journal:  Front Cell Dev Biol       Date:  2021-02-11
  6 in total

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