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Differential expression of CK20, ß-catenin, and MUC2/5AC/6 in Lynch syndrome and familial colorectal cancer type X.
Haraldsson, Stefan; Klarskov, Louise; Nilbert, Mef; Bernstein, Inge; Bonde, Jesper; Holck, Susanne.
Afiliação
  • Haraldsson S; Department of Gastroenterology, Copenhagen University Hospital, Kettegaard Alle 29, DK-2650 Hvidovre, Denmark.
  • Klarskov L; Department of Pathology, Herlev-Gentofte Hospital, Herlev, Denmark.
  • Nilbert M; Clinical Research Centre, HNPCC register, Copenhagen University Hospital, Hvidovre, Denmark.
  • Bernstein I; Institute of Clinical Sciences, Division of Oncology, Lund University, Lund, Sweden.
  • Bonde J; HNPCC register, Copenhagen University Hospital, Hvidovre, Denmark.
  • Holck S; Department of Surgical Gastroenterology, Aalborg University Hospital, Aalborg, Denmark.
BMC Clin Pathol ; 17: 11, 2017.
Article em En | MEDLINE | ID: mdl-28824332
ABSTRACT

BACKGROUND:

Hereditary non-polyposis colorectal cancer comprises Lynch syndrome and familial colorectal cancer type X (FCCTX). Differences in genetics, demographics and histopathology have been extensively studied. The purpose of this study is to characterize their immunoprofile of markers other than MMR proteins.

METHODS:

We compared the expression patterns of cytokeratins (CK7 and CK20), mucins (MUC2/5 AC/6), CDX2 and ß-catenin in Lynch syndrome and FCCTX.

RESULTS:

Differences were identified for CK20 and nuclear ß-catenin, which were significantly more often expressed in FCCTX than in Lynch syndrome (p < 0.001), whereas MUC2, MUC5AC and MUC6 were overexpressed in Lynch syndrome tumors compared with FCCTX tumors (p = 0.001, < 0.01, and < 0.001, respectively). We observed no differences in the expression patterns of CK7 and CDX2.

CONCLUSIONS:

In summary, we identified significant differences in the immunoprofiles of colorectal cancers linked to FCCTX and Lynch syndrome with a more sporadic-like profile in the former group and a more distinct profile with frequent MUC6 positivity in the latter group.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BMC Clin Pathol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: BMC Clin Pathol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Dinamarca