Expression of novel neuroendocrine marker insulinoma-associated protein 1 (INSM1) in genitourinary high-grade neuroendocrine carcinomas: An immunohistochemical study with specificity analysis and comparison to chromogranin, synaptophysin, and CD56.


Journal

Pathology, research and practice
ISSN: 1618-0631
Titre abrégé: Pathol Res Pract
Pays: Germany
ID NLM: 7806109

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 08 01 2020
revised: 03 04 2020
accepted: 22 04 2020
pubmed: 10 5 2020
medline: 2 4 2021
entrez: 9 5 2020
Statut: ppublish

Résumé

Confirmation of genitourinary high-grade neuroendocrine carcinomas (GU-HGNECs) often requires immunohistochemical staining. Here we evaluated a novel neuroendocrine marker, insulinoma-associated protein 1 (INSM1), in GU-HGNECs with comparison to chromogranin, synaptophysin and CD56. Immunohistochemical expression of INSM1, chromogranin, synaptophysin, and CD56 was evaluated in 39 GU-HGNECs using full tissue sections [4 in kidney, 28 in urinary bladder, and 7 in prostate; 31 small cell carcinomas (SmCCs), 6 large cell neuroendocrine carcinomas (LCNECs), 2 mixed SmCC-LCNECs]. In 33 SmCCs/components, INSM1 showed similar sensitivity (93.9 %) to chromogranin (87.8 %), synaptophysin (93.9 %) and CD56 (87.8 %), and stained a similar percentage of tumor cells (52 %) to chromogranin (49 %) and CD56 (52 %), but lower than synaptophysin (87 %) (p < 0.0001). In 8 LCNECs/components, INSM1 is similar to chromogranin, synaptophysin or CD56 in sensitivity (62.5 %, 62.5 %, 75 %, 62.5 %, respectively) and the mean percentage of positively stained tumor cells (21 %, 44 %, 48 %, 37 %, respectively). INSM1 is more sensitive for SmCCs than LCNECs (93.9 % vs. 62.5 %, p = 0.015). INSM1 showed 97.4 % specificity upon analyzing 273 genitourinary non-neuroendocrine tumors on tissue microarrays. Our study indicates that INSM1 is a sensitive marker for genitourinary HGNECs with high specificity. For genitourinary SmCCs, INSM1 shows similar sensitivity to chromogranin, synaptophysin and CD56 but stains a lower percentage of tumor cells than synaptophysin. For genitourinary LCNECs, INSM1 showed similar sensitivity to chromogranin, synaptophysin and CD56. INSM1 is more sensitive for genitourinary SmCCs than LCNECs. Our result and literature review indicate that whether INSM1 is more sensitive than conventional neuroendocrine markers for HGNECs depends on the tumor primary sites.

Identifiants

pubmed: 32381384
pii: S0344-0338(20)30061-3
doi: 10.1016/j.prp.2020.152993
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
CD56 Antigen 0
Chromogranins 0
NCAM1 protein, human 0
Repressor Proteins 0
SYP protein, human 0
Synaptophysin 0
INSM1 protein, human 147955-03-1

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152993

Informations de copyright

Copyright © 2020 Elsevier GmbH. All rights reserved.

Auteurs

Jie-Fu Chen (JF)

Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, USA.

Chen Yang (C)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Yue Sun (Y)

Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.

Dengfeng Cao (D)

Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, USA. Electronic address: dengfengcao@wustl.edu.

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Classifications MeSH