Human Tissue Kallikreins in Polymorphous Adenocarcinoma: A Polymerase Chain Reaction and Immunohistochemical Study.


Journal

Head and neck pathology
ISSN: 1936-0568
Titre abrégé: Head Neck Pathol
Pays: United States
ID NLM: 101304010

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 25 05 2020
accepted: 20 06 2020
pubmed: 28 6 2020
medline: 12 11 2021
entrez: 28 6 2020
Statut: ppublish

Résumé

Polymorphous adenocarcinoma (PAC) is the second most common malignant salivary gland tumour of minor salivary glands. Human tissue kallikreins (KLKs) are a family of highly conserved serine proteases expressed by various tissues and organs. The literature demonstrates a link between KLKs and salivary gland neoplasms. The purpose of this study was to determine levels of KLK mRNA in tissue samples of PAC and to determine if KLK expression is limited to tumour cells. Nineteen cases of PAC were reviewed (1987-2013). The diagnosis was confirmed, demographic data was collected, and formalin fixed paraffin-embedded PAC and normal salivary gland tissue samples were obtained. RNA isolation was achieved, followed by conversion to complementary DNA via reverse transcription. Using PCR, the quantitative level of expression of KLKs1-15 was recorded. Samples exhibiting high and low KLK expression were selected for immunohistochemistry staining. Results revealed a statistically significant increase in mean KLK mRNA expression for KLK1, KLK4, KLK10, KLK12 and KLK15 in PAC tissue samples, compared with normal salivary gland tissue (Mann-Whitney U test, p < 0.05). Immunohistochemistry results demonstrated that KLKs were present in tumor cells. Notably, all samples demonstrating relatively higher KLK mRNA expression showed equivalent or increased staining scores relative to the low KLK mRNA expression samples. In conclusion, there appears to be aberrant kallikrein expression in polymorphous adenocarcinoma, suggesting the possibility of a kallikrein cascade influence on tumor development and progression.

Identifiants

pubmed: 32592124
doi: 10.1007/s12105-020-01196-2
pii: 10.1007/s12105-020-01196-2
pmc: PMC8010004
doi:

Substances chimiques

Biomarkers, Tumor 0
Tissue Kallikreins EC 3.4.21.35

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

169-178

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Auteurs

Jacqueline Cox (J)

Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.

Zia Khan (Z)

Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.

Linda Jackson-Boeters (L)

Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.

Jerrold Armstrong (J)

Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.

Mark Darling (M)

Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada. mdarlin@uwo.ca.
Department of Pathology and Laboratory Medicine, University of Western Ontario, 1151 Richmond Street, HSA 424, London, ON, N6A 5C1, Canada. mdarlin@uwo.ca.

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Classifications MeSH