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[Morphological and immunohistochemical characteristics of the molecular subtypes of urothelial carcinomas]. / Morfologicheskaia i immunogistokhimicheskaia kharakteristika molekuliarnykh podtipov urotelial'nykh kartsinom.
Osmanov, Yu I; Gaibov, Zh A; Kogan, E A; Radenska-Lopovok, S G; Tursunov, Kh Z.
Afiliação
  • Osmanov YI; Acad. A.I. Strukov Department of Anatomic Pathology, I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia; Department of Anatomic Pathology, Research Clinical Center of the OAO RhD, Moscow, Russia.
  • Gaibov ZA; Department of Anatomic Pathology, Research Clinical Center of the OAO RhD, Moscow, Russia.
  • Kogan EA; Acad. A.I. Strukov Department of Anatomic Pathology, I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia.
  • Radenska-Lopovok SG; Acad. A.I. Strukov Department of Anatomic Pathology, I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia.
  • Tursunov KZ; Department of Anatomic Pathology, Tashkent Medical Academy, Tashkent, Republic of Uzbekistan.
Arkh Patol ; 81(5): 35-44, 2019.
Article em Ru | MEDLINE | ID: mdl-31626203
ABSTRACT
The molecular subtypes of urothelial carcinoma in each classification scheme have characteristic immunohistochemical features. At the same time, the results of conducted studies often demonstrate a discrepancy between the genomic profile of urothelial carcinoma and its immunophenotype, which complicates the immunohistochemical verification of the molecular subtypes of these tumors.

OBJECTIVE:

To compare the morphological and immunophenotypic characteristics of the molecular subtypes of urothelial carcinoma. MATERIAL AND

METHODS:

Surgical specimens from 196 patients diagnosed with urothelial carcinoma of the renal pelvis and bladder were investigated. Paraffin-embedded sections were immunohistochemically examined using the standard protocol. Antibodies against CK5/6, CK17, Rb1 (Dako), CK14, CK18, CK20, Cyclin D1, Cyclin E1, Cyclin A, Cyclin B, Chromogranin, E-Cadherin, P-Cadherin, p16, Uroplakin II, TUBB2B, Vimentin, ZEB-2 ('Novocastra'), CD44, GATA-3, and Uroplakin III ('Cell Marque') were used.

RESULTS:

Out of 68 (35%) superficial papillary urothelial carcinomas, 24 (12%) tumors constituted Molecular Class I and 12 (6%) and 32 (16%) ones did Molecular Classes II and III, respectively. Of the 128 (65%) muscle-invasive urothelial carcinomas, 57 (29%) tumors were referred to as the luminal-papillary molecular subtype, and 24 (12%) and 14 (7%) were as the luminal-infiltrated and luminal molecular subtypes, respectively. The basal squamous molecular subtype was verified in 31 (16%) neoplasms and the neuronal phenotype was detected in 2 (1%) cases.

CONCLUSION:

Most pT1 tissues correspond to Molecular Class II. In the muscle-invasive urothelial carcinoma group, the neoplasms with a luminal phenotype predominate over the tumors with basal and neuronal phenotypes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Urológicas Tipo de estudo: Guideline Limite: Humans Idioma: Ru Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Urológicas Tipo de estudo: Guideline Limite: Humans Idioma: Ru Ano de publicação: 2019 Tipo de documento: Article