NET G3 vs NEC: p53 and Rb1 Immunolabeling in High-grade Gastrointestinal Neuroendocrine Neoplasms - Is It Enough for the Differential Diagnosis?


Journal

Journal of gastrointestinal and liver diseases : JGLD
ISSN: 1842-1121
Titre abrégé: J Gastrointestin Liver Dis
Pays: Romania
ID NLM: 101272825

Informations de publication

Date de publication:
22 06 2023
Historique:
received: 12 10 2022
accepted: 07 04 2023
medline: 23 6 2023
pubmed: 22 6 2023
entrez: 22 6 2023
Statut: epublish

Résumé

High-grade gastrointestinal neuroendocrine neoplasms (GI-NENs) are divided into well-differentiated G3 neuroendocrine tumors (NETs G3) and neuroendocrine carcinomas (NECs), having identical cut-offs of proliferation, but different biomolecular origins. This translates in distinct treatment choices. Our aim was to establish if p53/Rb1 immunohistochemical status in GI-NENs with Ki67 index >20% can predict the histopathological diagnosis. p53/Rb1 immunolabelling was performed on 42 cases of high-grade GI-NENs, diagnosed as NET G3, NEC and mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) with NEC component. Immunolabeled slides were digitally scanned, with automatic quantification of p53 and Rb1, blind to the diagnosis. The p53 positive percentage was stratified; two cut-offs were selected, naming the intervals as N (null, <1%), T (tumor, 1%-20%) and C (carcinoma, >20%). The Rb1 expression loss in >90% of neoplastic cells was considered mutational. NETs G3 mainly showed the T status (14/16, 87.5%), followed by N (1/16, 6.25%) and C (1/16, 6.25%); NECs and NEC components in MiNENs predominantly expressed the C status (19/26, 73.08%), followed by N (5/26, 19.23%) and T (2/26, 7.69%) (p<0.001, χ 2 =27.017). NET G3s showed positive expression for Rb1; 73.08% of NECs expressed negative Rb1 (p<0.001, χ 2 =21.351). NECs and NEC components in MiNENs showed Rb1 mutational status in 13 C cases (13/19, 68.42%), 4 N cases (4/5, 80%) and in both the T cases (p=0.002, χ 2 =11.187). Our results highlight the correlations between the p53/Rb1 immunostainings and the histopathological diagnosis of high-grade GI-NENs. NECs and NEC components in MiNENs showed a p53 mutational status (0% or 21-100%) and predominantly negative Rb1 expression. NETs G3 showed a p53 wild-type status (1-20%) and retained Rb1 expression. These findings suggest that the differential diagnosis of high-grade GI-NENs may benefit from p53/Rb1 immunohistochemical tests in everyday practice.

Sections du résumé

BACKGROUND AND AIMS
High-grade gastrointestinal neuroendocrine neoplasms (GI-NENs) are divided into well-differentiated G3 neuroendocrine tumors (NETs G3) and neuroendocrine carcinomas (NECs), having identical cut-offs of proliferation, but different biomolecular origins. This translates in distinct treatment choices. Our aim was to establish if p53/Rb1 immunohistochemical status in GI-NENs with Ki67 index >20% can predict the histopathological diagnosis.
METHODS
p53/Rb1 immunolabelling was performed on 42 cases of high-grade GI-NENs, diagnosed as NET G3, NEC and mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) with NEC component. Immunolabeled slides were digitally scanned, with automatic quantification of p53 and Rb1, blind to the diagnosis.
RESULTS
The p53 positive percentage was stratified; two cut-offs were selected, naming the intervals as N (null, <1%), T (tumor, 1%-20%) and C (carcinoma, >20%). The Rb1 expression loss in >90% of neoplastic cells was considered mutational. NETs G3 mainly showed the T status (14/16, 87.5%), followed by N (1/16, 6.25%) and C (1/16, 6.25%); NECs and NEC components in MiNENs predominantly expressed the C status (19/26, 73.08%), followed by N (5/26, 19.23%) and T (2/26, 7.69%) (p<0.001, χ 2 =27.017). NET G3s showed positive expression for Rb1; 73.08% of NECs expressed negative Rb1 (p<0.001, χ 2 =21.351). NECs and NEC components in MiNENs showed Rb1 mutational status in 13 C cases (13/19, 68.42%), 4 N cases (4/5, 80%) and in both the T cases (p=0.002, χ 2 =11.187).
CONCLUSIONS
Our results highlight the correlations between the p53/Rb1 immunostainings and the histopathological diagnosis of high-grade GI-NENs. NECs and NEC components in MiNENs showed a p53 mutational status (0% or 21-100%) and predominantly negative Rb1 expression. NETs G3 showed a p53 wild-type status (1-20%) and retained Rb1 expression. These findings suggest that the differential diagnosis of high-grade GI-NENs may benefit from p53/Rb1 immunohistochemical tests in everyday practice.

Identifiants

pubmed: 37345605
doi: 10.15403/jgld-4654
doi:

Substances chimiques

Tumor Suppressor Protein p53 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

162-169

Auteurs

Alexandra Dinu (A)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta, Romania. . amaiorean@yahoo.co.uk.

Mariana Aschie (M)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Medicine Faculty, Ovidius University of Constanta, Constanta; Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, Ovidius University of Constanta, Constanta, Romania. aschiemariana@yahoo.com.

Georgeta Camelia Cozaru (GC)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, Ovidius University of Constanta, Constanta, Romania. drcozaru@yahoo.com.

Anca Florentina Mitroi (AF)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, Ovidius University of Constanta, Constanta, Romania. ank_mitroi@yahoo.com.

Catalin Nicolae Grasa (CN)

Medicine Faculty, Ovidius University of Constanta, Constanta; Surgery Department, Sf. Apostol Andrei Emergency County Hospital, Constanta, Romania. catalin.grasa@yahoo.com.

Ionut Eduard Iordache (IE)

Medicine Faculty, Ovidius University of Constanta, Constanta; Surgery Department, Sf. Apostol Andrei Emergency County Hospital, Constanta, Romania. eduardiordache@yahoo.com.

Mariana Deacu (M)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Medicine Faculty, Ovidius University of Constanta, Constanta, Romania. deacu_mariana@yahoo.com.

Cristian Ionut Orasanu (CI)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, Ovidius University of Constanta, Constanta, Romania. critian.ionut@gmail.com.

Antonela-Anca Nicolau (AA)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, Ovidius University of Constanta, Constanta, Romania. ancanicolau@rocketmail.com.

Gabriela Izabela Baltatescu (GI)

Clinical Service of Pathology, Sf. Apostol Andrei Emergency County Hospital, Constanta; Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology, Ovidius University of Constanta, Constanta, Romania. gabrielabaltatescu@yahoo.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH