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主要的细胞和基质类型如何协同作用以预测头颈部腺样囊性癌的预后?

How predominant cell and stroma types harmonize to predict head and neck adenoid cystic carcinoma outcomes?

作者信息

John Sharon, Jain Ayushi, Devi Priya, Gupta Shalini, Raghuvanshi Shivanjali

机构信息

Resident (Oral Pathology), King George's Medical University, Lucknow, UP, India.

Professor & Head (Oral Pathology), King George's Medical University, Lucknow, UP, India.

出版信息

Med J Armed Forces India. 2024 Jul-Aug;80(4):404-411. doi: 10.1016/j.mjafi.2024.05.012. Epub 2024 Jun 21.


DOI:10.1016/j.mjafi.2024.05.012
PMID:39071760
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11279721/
Abstract

Adenoid cystic carcinoma (ACC) is an uncommon tumor that usually appears in the major salivary glands of the head and neck region, including the minor glands in the oral cavity, sinonasal tract, and other sites. ACC of the head and neck may have a low-grade histological appearance. This malignant tumor has unusual clinical characteristics such as occasional regional lymph node metastases and a prolonged yet continuously advancing clinical course. Additionally, it is an invasive tumor with perineural invasion, difficult-to-clear margins, metastasis, and localized recurrence. The cribriform and tubular proliferation of basaloid cells, which mostly display a myoepithelial cellular phenotype, are ACC's distinct histologic characteristics. The degree of genetic alterations and aneuploidy observed in tumor genomes are linked to the severity of histologic grade, which correlates with clinical prognosis. The three predominant cell types (PCTs) i.e., conventional ACC (C-ACC), myoepithelial-predominant ACC (M-ACC), and epithelial-predominant ACC (E-ACC)-and their respective applications will be reviewed. The function of extracellular matrix (ECM) components such as laminin, type IV collagen, fibronectin, and tenascin are also emphasized. An attempt has been made to explore the recent molecular diversity, regulatory pathways prevalent in PCT, ECM with its genetic changes, and translational utility with targeted therapies for ACC.

摘要

腺样囊性癌(ACC)是一种罕见的肿瘤,通常出现在头颈部的大唾液腺,包括口腔、鼻窦道及其他部位的小唾液腺。头颈部的ACC可能具有低级别组织学表现。这种恶性肿瘤具有不寻常的临床特征,如偶见区域淋巴结转移和漫长但持续进展的临床病程。此外,它是一种具有神经周围浸润、切缘难以清除、转移和局部复发的浸润性肿瘤。基底样细胞呈筛状和管状增生,大多表现为肌上皮细胞表型,这是ACC独特的组织学特征。肿瘤基因组中观察到的基因改变程度和非整倍体与组织学分级的严重程度相关,而组织学分级又与临床预后相关。本文将对三种主要细胞类型,即传统ACC(C-ACC)、肌上皮为主型ACC(M-ACC)和上皮为主型ACC(E-ACC)及其各自的应用进行综述。还将强调细胞外基质(ECM)成分如层粘连蛋白、IV型胶原、纤连蛋白和腱生蛋白的功能。本文试图探讨ACC最近的分子多样性、主要细胞类型中普遍存在的调控途径、具有基因变化的ECM以及靶向治疗的转化应用。

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本文引用的文献

[1]
Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications.

Front Oncol. 2023-7-5

[2]
Heterogeneity and versatility of the extracellular matrix during the transition from pleomorphic adenoma to carcinoma ex pleomorphic adenoma: cumulative findings from basic research and new insights.

Front Oral Health. 2023-4-17

[3]
Invasion-Associated Reorganization of Laminin 332 in Oral Squamous Cell Carcinomas: The Role of the Laminin γ2 Chain in Tumor Biology, Diagnosis, and Therapy.

Cancers (Basel). 2022-10-7

[4]
Clinical disease course and survival outcomes following disease recurrence in adenoid cystic carcinoma with and without NOTCH signaling pathway activation.

Oral Oncol. 2022-10

[5]
Paired related homeobox 1 attenuates autophagy via acetyl-CoA carboxylase 1-regulated fatty acid metabolism in salivary adenoid cystic carcinoma.

FEBS Open Bio. 2022-5

[6]
Dominant cell type analysis predicts head and neck adenoid cystic carcinoma outcomes.

Ann Diagn Pathol. 2022-2

[7]
Matrix metalloproteinase-7, -8, -9, -15, and -25 in minor salivary gland adenoid cystic carcinoma.

Pathol Res Pract. 2021-1

[8]
Expression Profiling of Extracellular Matrix Genes Reveals Global and Entity-Specific Characteristics in Adenoid Cystic, Mucoepidermoid and Salivary Duct Carcinomas.

Cancers (Basel). 2020-8-31

[9]
The Matrix Revolution: Matricellular Proteins and Restructuring of the Cancer Microenvironment.

Cancer Res. 2020-3-19

[10]
Phase II Study of Lenvatinib in Patients With Progressive, Recurrent or Metastatic Adenoid Cystic Carcinoma.

J Clin Oncol. 2019-4-2

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