Expression of HMB45, MelanA and SOX10 is rare in non-small cell lung cancer

被引:8
作者
Kriegsmann, Mark [1 ]
Kriegsmann, Katharina [2 ]
Harms, Alexander [1 ,3 ,4 ]
Longuespee, Remi [1 ]
Zgorzelski, Christiane [1 ]
Leichsenring, Jonas [1 ]
Muley, Thomas [3 ,4 ,5 ]
Winter, Hauke [3 ,4 ,6 ]
Kazdal, Daniel [1 ,3 ,4 ]
Goeppert, Benjamin [1 ]
Warth, Arne [1 ,7 ]
机构
[1] Univ Hosp Heidelberg, Inst Pathol, Neuenheimer Feld 224, Heidelberg, Germany
[2] Univ Hosp Heidelberg, Dept Internal Med Hematol Oncol & Rheumatol 5, Heidelberg, Germany
[3] Translat Lung Res Ctr Heidelberg, Heidelberg, Germany
[4] German Ctr Lung Res, Heidelberg, Germany
[5] Heidelberg Univ, Thoraxklin, Translat Res Unit, Heidelberg, Germany
[6] Heidelberg Univ, Thoraxklin, Dept Thorac Surg, Heidelberg, Germany
[7] UEGP, Inst Pathol Cytopathol & Mol Pathol, Wetzlar, Limburg, Germany
关键词
NSCLC; Lung cancer; SOX10; HMB45; MelanA; Immunohistochemistry; MALIGNANT-MELANOMA; LARGE-SCALE; TUMORS; CARCINOMA; PULMONARY; IMMUNOMARKERS; MORPHOLOGY; DIAGNOSIS; EMPHASIS; UTILITY;
D O I
10.1186/s13000-018-0751-7
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Non-small cell lung cancer (NSCLC) and melanoma are frequent entities in routine diagnostics. Whereas the differential diagnosis is usually straight forward based on histomorphology, it can be challenging in poorly differentiated tumors as melanoma may mimic various histological patterns. Distinction of the two entities is of outmost importance as both are treated differently. HMB45 and MelanA are recommended immunohistological markers for melanoma in this scenario. SOX10 has been described as an additional marker for melanoma. However, comprehensive large-scale data about the expression of melanoma markers in NSCLC tumor tissue specimen are lacking so far. Methods: Therefore, we analyzed the expression of these markers in 1085 NSCLC tumor tissue samples. Tissue microarrays of NSCLC cases were immunohistochemically stained for HMB45, MelanA, and SOX10. Positivity of a marker was defined as >= 1% positive tumor cells. Results: In 1027 NSCLC tumor tissue samples all melanoma as well as conventional immunohistochemical markers for NSCLC could be evaluated. HMB45, MelanA, and SOX10 were positive in 1 (< 1%), 0 (0%) and 5 (< 1%) cases. The HMB45 positive case showed co-expression of SOX10 and was classified as large cell carcinoma. Three out of five SOX10 positive cases were SqCC and one case was an adenosquamous carcinoma. Conclusions: Expression of HMB45, MelanA and SOX10 is evident but exceedingly rare in NSCLC cases. Together with conventional immunomarkers a respective marker panel allows a clear-cut differential diagnosis even in poorly differentiated tumors.
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页数:6
相关论文
共 46 条
[41]   Primary melanoma of the lung: A clinicopathologic and immunohistochemical study of eight cases [J].
Wilson, RW ;
Moran, CA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (10) :1196-1202
[42]  
Yamamoto Y, 2017, MOL CLIN ONCOL, V7, P39, DOI 10.3892/mco.2017.1256
[43]   SOX10 is over-expressed in bladder cancer and contributes to the malignant bladder cancer cell behaviors [J].
Yin, H. ;
Qin, C. ;
Zhao, Y. ;
Du, Y. ;
Sheng, Z. ;
Wang, Q. ;
Song, Q. ;
Chen, L. ;
Liu, C. ;
Xu, T. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2017, 19 (08) :1035-1044
[44]   High expression of Sox10 correlates with tumor aggressiveness and poor prognosis in human nasopharyngeal carcinoma [J].
Zhao, Yu ;
Liu, Zhi-gang ;
Tang, Jiao ;
Zou, Ren-fang ;
Chen, Xiao-yan ;
Jiang, Guan-min ;
Qiu, Yan-fang ;
Wang, Hui .
ONCOTARGETS AND THERAPY, 2016, 9 :1671-1677
[45]   SOXs in human prostate cancer: implication as progression and prognosis factors [J].
Zhong, Wei-de ;
Qin, Guo-qiang ;
Dai, Qi-shan ;
Han, Zhao-dong ;
Chen, Shan-ming ;
Ling, Xiao-hui ;
Fu, Xin ;
Cai, Chao ;
Chen, Jia-hong ;
Chen, Xi-bin ;
Lin, Zhuo-yuan ;
Deng, Ye-han ;
Wu, Shu-lin ;
He, Hui-chan ;
Wu, Chin-lee .
BMC CANCER, 2012, 12
[46]   SOX10 is a novel oncogene in hepatocellular carcinoma through Wnt/β-catenin/TCF4 cascade [J].
Zhou, Dangjun ;
Bai, Fengjiao ;
Zhang, Xinning ;
Hu, Minggen ;
Zhao, Guodong ;
Zhao, Zhiming ;
Liu, Rong .
TUMOR BIOLOGY, 2014, 35 (10) :9935-9940