Mucin phenotypes and clinicopathological features of colorectal adenocarcinomas: Correlation with colorectal adenocarcinoma with enteroblastic differentiation.


Journal

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

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 06 12 2021
revised: 08 03 2022
accepted: 09 03 2022
pubmed: 19 3 2022
medline: 6 4 2022
entrez: 18 3 2022
Statut: ppublish

Résumé

The mucin phenotypes of colorectal carcinoma (CRC) is related to the biological behavior and prognosis. But there has been no studies evaluating phenotypic characteristics in a large number of cases. Furthermore, colorectal adenocarcinoma with enteroblastic differentiation (CAED) is a rare subtype of CRC and having poor prognosis. The aims of this study were to clarify the correlation between mucin phenotypes and tumor development, including biological behavior in CRC, as well as to investigate characteristic of mucin phenotypes in CAED. 974 CRC cases and 42 CAED cases of CRCs were classified five types (large-intestinal, small-intestinal, gastric, mixed, and unclassified) of mucin phenotypes by using immunohistochemistry (IHC). IHC was performed on tissue microarrays with antibodies against followings: MUC2, MUC5AC, MUC6, and CD10. In CRCs, large-intestine type has a relatively better prognosis, small-intestinal type frequently shows venous invasions, and liver metastases, gastric type has more high-histological grades and lymphatic invasions, mixed type shows originating from the right side of the colon, larger tumor size and mucinous type, but less venous invasions and liver metastasis, whereas the unclassified type showed poorer prognosis in overall survival with statistical significance. The majority of CAED were found to be small-intestinal type or unclassified type. The phenotypic classification is useful for predicting the prognosis of CRCs. Small-intestinal type and unclassified type showed dismal prognosis in CRCs. We speculate that CAED having aggressive behavior and poor prognosis might reflect characteristics of small-intestinal and unclassified types.

Sections du résumé

BACKGROUND BACKGROUND
The mucin phenotypes of colorectal carcinoma (CRC) is related to the biological behavior and prognosis. But there has been no studies evaluating phenotypic characteristics in a large number of cases. Furthermore, colorectal adenocarcinoma with enteroblastic differentiation (CAED) is a rare subtype of CRC and having poor prognosis. The aims of this study were to clarify the correlation between mucin phenotypes and tumor development, including biological behavior in CRC, as well as to investigate characteristic of mucin phenotypes in CAED.
METHODS AND RESULTS RESULTS
974 CRC cases and 42 CAED cases of CRCs were classified five types (large-intestinal, small-intestinal, gastric, mixed, and unclassified) of mucin phenotypes by using immunohistochemistry (IHC). IHC was performed on tissue microarrays with antibodies against followings: MUC2, MUC5AC, MUC6, and CD10. In CRCs, large-intestine type has a relatively better prognosis, small-intestinal type frequently shows venous invasions, and liver metastases, gastric type has more high-histological grades and lymphatic invasions, mixed type shows originating from the right side of the colon, larger tumor size and mucinous type, but less venous invasions and liver metastasis, whereas the unclassified type showed poorer prognosis in overall survival with statistical significance. The majority of CAED were found to be small-intestinal type or unclassified type.
CONCLUSIONS CONCLUSIONS
The phenotypic classification is useful for predicting the prognosis of CRCs. Small-intestinal type and unclassified type showed dismal prognosis in CRCs. We speculate that CAED having aggressive behavior and poor prognosis might reflect characteristics of small-intestinal and unclassified types.

Identifiants

pubmed: 35303523
pii: S0344-0338(22)00083-8
doi: 10.1016/j.prp.2022.153840
pii:
doi:

Substances chimiques

Mucin-1 0
Mucin-2 0
Mucin-6 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

153840

Informations de copyright

Copyright © 2022 Elsevier GmbH. All rights reserved.

Auteurs

Taro Kurosawa (T)

Department of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan; Department of Human Pathology, Juntendo University School of Medicine, Tokyo, Japan.

Takashi Murakami (T)

Department of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan.

Yuya Yamashiro (Y)

Department of Gastroenterology and Hepatology, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.

Hiroyuki Terukina (H)

Department of Human Pathology, Juntendo University School of Medicine, Tokyo, Japan.

Takuo Hayashi (T)

Department of Human Pathology, Juntendo University School of Medicine, Tokyo, Japan.

Tsuyoshi Saito (T)

Department of Human Pathology, Juntendo University School of Medicine, Tokyo, Japan.

Shuko Nojiri (S)

Department of Medical Technology Innovation Center, Juntendo University School of Medicine, Tokyo, Japan.

Kazuhiro Sakamoto (K)

Department of Coloproctological Surgery, Juntendo University Faculty of Medicine, Tokyo, Japan.

Akihito Nagahara (A)

Department of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan.

Takashi Yao (T)

Department of Human Pathology, Juntendo University School of Medicine, Tokyo, Japan. Electronic address: tyao@juntendo.ac.jp.

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