Expression of neural cell adhesion molecule L1 (CD171) in neuroectodermal and other tumors. An immunohistochemical study of 5155 tumors and critical evaluation of CD171 prognostic value in gastrointestinal stromal tumors

被引:21
作者
Inaguma, Shingo [1 ,2 ]
Wang, Zengfeng [1 ]
Lasota, Jerzy P. [1 ]
Miettinen, Markku M. [1 ]
机构
[1] NCI, Pathol Lab, Bldg 10, Bethesda, MD 20892 USA
[2] Aichi Med Univ, Dept Pathol, Sch Med, Nagakute, Aichi, Japan
关键词
CD171; (NCAM-L1; L1CAM); immunohistochemistry; neuroectodermal tumor; gastrointestinal stromal tumor; mismatch repair deficiency; IMMUNOGLOBULIN SUPERFAMILY; RECOGNITION MOLECULES; MEDIATED RELEASE; AXON GUIDANCE; L1CAM; L1-CAM; PROTEIN; NEUROBLASTOMA; ANTIBODIES; EPITOPE;
D O I
10.18632/oncotarget.10527
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The neural cell adhesion molecule L1 (CD171) is a multidomain type 1 membrane glycoprotein of the immunoglobulin superfamily important in the nervous system development, kidney morphogenesis, and maintenance of the immune system. Recent studies reported CD171 expression being associated with adverse clinical outcome in different types of cancer and there has been a growing interest in targeting this cell membrane molecule on neoplastic cells by chimeric antigen receptor redirected T lymphocytes or specific antibodies. Nevertheless, conflicting results regarding the prognostic value of CD171 expression in renal cell carcinomas and gastrointestinal stromal tumors were published. In this study, CD171 expression was immunohistochemically analyzed in 5155 epithelial, mesenchymal, melanocytic, and lymphohematopoietic tumors to assess its utility in diagnostic pathology and to pinpoint potential targets for CD171-targeting therapy. A newly developed anti-CD171 rabbit monoclonal antibody, clone 014, was selected from the panel of commercially available CD171 antibodies. Immunohistochemistry was performed using Leica Bond Max automation and multitumor blocks containing up to 60 tumor samples. CD171 was constitutively and strongly expressed in neuroectodermal tumors such as schwannoma, neuroblastoma, and paraganglioma, whereas other mesenchymal tumors including schwannoma mimics showed only rarely CD171 positivity. Frequent CD171-expression was also detected in ovarian serous carcinoma, malignant mesothelioma, and testicular embryonal carcinoma. CD171 immunohistochemistry may have some role in immunophenotypic differential diagnosis of neurogenic tumors and pinpointing potential candidates for anti-CD171 therapy. Though, because of its rare expression and lack of predictive value, CD171 is neither a diagnostic nor prognostic marker for gastrointestinal stromal tumors.
引用
收藏
页码:55276 / 55289
页数:14
相关论文
共 41 条
  • [31] L1 is Highly Expressed in Tumors of the Nervous System: A Study of Over 8000 Human Tissues
    Rawnaq, Tamina
    Quaas, Alexander
    Zander, Hilke
    Gros, Stephanie J.
    Reichelt, Uta
    Blessmann, Marco
    Wilzcak, Waldemar
    Schachner, Melitta
    Sauter, Guido
    Izbicki, Jakob R.
    Kaifi, Jussuf T.
    [J]. JOURNAL OF SURGICAL RESEARCH, 2012, 173 (02) : 314 - 319
  • [32] Neural recognition molecules and synaptic plasticity
    Schachner, M
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (05) : 627 - 634
  • [33] Combined treatment of L1CAM antibodies and cytostatic drugs improve the therapeutic response of pancreatic and ovarian carcinoma
    Schaefer, Heiner
    Dieckmann, Chantal
    Korniienko, Olena
    Moldenhauer, Gerhard
    Kiefel, Helena
    Salnikov, Alexey
    Krueger, Achim
    Altevogt, Peter
    Sebens, Susanne
    [J]. CANCER LETTERS, 2012, 319 (01) : 66 - 82
  • [34] Role of miR-34a as a suppressor of L1CAM in endometrial carcinoma
    Schirmer, Uwe
    Doberstein, Kai
    Rupp, Anne-Kathleen
    Bretz, Niko P.
    Wuttig, Daniela
    Kiefel, Helena
    Breunig, Christian
    Fiegl, Heidi
    Mueller-Holzner, Elisabeth
    Zeillinger, Robert
    Schuster, Eva
    Zeimet, Alain G.
    Sueltmann, Holger
    Altevogt, Peter
    [J]. ONCOTARGET, 2014, 5 (02) : 462 - 472
  • [35] Expression and prognostic value of L1-CAM in breast cancer
    Schroeder, Christine
    Schumacher, Udo
    Fogel, Mina
    Feuerhake, Friedrich
    Mueller, Volkmar
    Wirtz, Ralph M.
    Altevogt, Peter
    Krenkel, Sylke
    Jaenicke, Fritz
    Milde-Langosch, Karin
    [J]. ONCOLOGY REPORTS, 2009, 22 (05) : 1109 - 1117
  • [36] Diagnostic and prognostic markers for gastrointestinal stromal tumors in Norway
    Steigen, Sonja E.
    Bjerkehagen, Bodil
    Haugland, Hans K.
    Nordrum, Ivar S.
    Loberg, Else Marit
    Isaksen, Vidar
    Eide, Tor J.
    Nielsen, Torsten O.
    [J]. MODERN PATHOLOGY, 2008, 21 (01) : 46 - 53
  • [37] L1CAM protein expression is associated with poor prognosis in non-small cell lung cancer
    Tischler, Verena
    Pfeifer, Marco
    Hausladen, Silke
    Schirmer, Uwe
    Bonde, Anne-Katrine
    Kristiansen, Glen
    Sos, Martin L.
    Weder, Walter
    Moch, Holger
    Altevogt, Peter
    Soltermann, Alex
    [J]. MOLECULAR CANCER, 2011, 10 : 127
  • [38] L1 is associated with favorable outcome in neuroblastomas in contrast to adult tumors
    Wachowiak, Robin
    Fiegel, Henning C.
    Kaifi, Jussuf T.
    Quaas, Alexander
    Krickhahn, Annika
    Schurr, Paulus G.
    Erttmann, Rudolf
    Schachner, Melitta
    Kluth, Dietrich
    Sauter, Guido
    Izbicki, Jakob R.
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2007, 14 (12) : 3575 - 3580
  • [39] Circulating levels of cell adhesion molecule L1 as a prognostic marker in gastrointestinal stromal tumor patients
    Zander, Hilke
    Rawnaq, Tamina
    von Wedemeyer, Max
    Tachezy, Michael
    Kunkel, Miriam
    Wolters, Gerrit
    Bockhorn, Maximilian
    Schachner, Melitta
    Izbicki, Jakob R.
    Kaifi, Jussuf
    [J]. BMC CANCER, 2011, 11
  • [40] The differential role of L1 in ovarian carcinoma and normal ovarian surface epithelium
    Zeechini, Silvia
    Bianchi, Marco
    Colombo, Nicoletta
    Fasani, Roberta
    Goisis, Giovanni
    Casadio, Chiara
    Viale, Giuseppe
    Liu, Jinsong
    Herlyn, Meenhard
    Godwin, Andrew K.
    Nuciforo, Paolo G.
    Cavallaro, Ugo
    [J]. CANCER RESEARCH, 2008, 68 (04) : 1110 - 1118