Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?

Warthin’s tumor is the second most frequent neoplasm next to pleomorphic adenoma in the salivary gland, mostly in the parotid gland. The epithelial cells constituting a tumor are characterized by the presence of mitochondria that undergo structural and functional changes, resulting in the developmen...

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Main Authors: Ryogo Aoki, Takuji Tanaka
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/16/5/912
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author Ryogo Aoki
Takuji Tanaka
author_facet Ryogo Aoki
Takuji Tanaka
author_sort Ryogo Aoki
collection DOAJ
description Warthin’s tumor is the second most frequent neoplasm next to pleomorphic adenoma in the salivary gland, mostly in the parotid gland. The epithelial cells constituting a tumor are characterized by the presence of mitochondria that undergo structural and functional changes, resulting in the development of oncocytes. In addition to containing epithelial cells, Warthin’s tumors contain abundant lymphocytes with lymph follicles (germinal centers) that are surrounded by epithelial cells. The pathogenesis of Warthin’s tumor is not fully understood, and several hypotheses have been proposed. The risk factors for the development of Warthin’s tumor, which predominantly occurs in males, include aging, smoking, and radiation exposure. Recently, it has been reported that chronic inflammation and aging cells promote the growth of Warthin’s tumor. Several reports regarding the origin of the tumor have suggested that (1) Warthin’s tumor is an IgG4-related disease, (2) epithelial cells that compose Warthin’s tumor accumulate mitochondria, and (3) Warthin’s tumor is a metaplastic lesion in the lymph nodes. It is possible that the pathogenesis of Warthin’s tumor includes mitochondrial metabolic abnormalities, accumulation of aged cells, chronic inflammation, and senescence-associated secretory phenotype (SASP). In this short review, we propose that DNA damage, metabolic dysfunction of mitochondria, senescent cells, SASP, human papillomavirus, and IgG4 may be involved in the development of Warthin’s tumor.
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spelling doaj.art-c1bf9661decf4fe182f37cdb1e254cd02024-03-12T16:40:48ZengMDPI AGCancers2072-66942024-02-0116591210.3390/cancers16050912Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?Ryogo Aoki0Takuji Tanaka1Department of Diagnostic Pathology (DDP) & Research Center of Diagnostic Pathology (RC-DiP), Gifu Municipal Hospital, 7-l Kashima-Cho, Gifu City 500-8513, Gifu, JapanDepartment of Diagnostic Pathology (DDP) & Research Center of Diagnostic Pathology (RC-DiP), Gifu Municipal Hospital, 7-l Kashima-Cho, Gifu City 500-8513, Gifu, JapanWarthin’s tumor is the second most frequent neoplasm next to pleomorphic adenoma in the salivary gland, mostly in the parotid gland. The epithelial cells constituting a tumor are characterized by the presence of mitochondria that undergo structural and functional changes, resulting in the development of oncocytes. In addition to containing epithelial cells, Warthin’s tumors contain abundant lymphocytes with lymph follicles (germinal centers) that are surrounded by epithelial cells. The pathogenesis of Warthin’s tumor is not fully understood, and several hypotheses have been proposed. The risk factors for the development of Warthin’s tumor, which predominantly occurs in males, include aging, smoking, and radiation exposure. Recently, it has been reported that chronic inflammation and aging cells promote the growth of Warthin’s tumor. Several reports regarding the origin of the tumor have suggested that (1) Warthin’s tumor is an IgG4-related disease, (2) epithelial cells that compose Warthin’s tumor accumulate mitochondria, and (3) Warthin’s tumor is a metaplastic lesion in the lymph nodes. It is possible that the pathogenesis of Warthin’s tumor includes mitochondrial metabolic abnormalities, accumulation of aged cells, chronic inflammation, and senescence-associated secretory phenotype (SASP). In this short review, we propose that DNA damage, metabolic dysfunction of mitochondria, senescent cells, SASP, human papillomavirus, and IgG4 may be involved in the development of Warthin’s tumor.https://www.mdpi.com/2072-6694/16/5/912Warthin’s tumorpathogenesisneoplasticSASPsenescent cellsDNA damage
spellingShingle Ryogo Aoki
Takuji Tanaka
Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?
Cancers
Warthin’s tumor
pathogenesis
neoplastic
SASP
senescent cells
DNA damage
title Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?
title_full Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?
title_fullStr Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?
title_full_unstemmed Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?
title_short Pathogenesis of Warthin’s Tumor: Neoplastic or Non-Neoplastic?
title_sort pathogenesis of warthin s tumor neoplastic or non neoplastic
topic Warthin’s tumor
pathogenesis
neoplastic
SASP
senescent cells
DNA damage
url https://www.mdpi.com/2072-6694/16/5/912
work_keys_str_mv AT ryogoaoki pathogenesisofwarthinstumorneoplasticornonneoplastic
AT takujitanaka pathogenesisofwarthinstumorneoplasticornonneoplastic