Literature DB >> 36169795

Simultaneous Expression of PD-1 and PD-L1 in Peripheral and Central Immune Cells and Tumor Cells in the Benign and Malignant Salivary Gland Tumors Microenvironment.

Mohammad Reza Haghshenas1, Nasrollah Erfani2,3, Sajjad Gerdabi4,5, Fatemeh Asadian6, Razie Kiani5, Bijan Khademi7.   

Abstract

BACKGROUND: To investigate the differential expression of PD-1 and PD-L1 in salivary gland tumors (SGTs, malignant and benign subtypes) and determine their association with the clinicopathological characterization of the patients.
METHODS: The immunohistochemistry was used to examine PD-1 and PD-L1 expression in specimens from 83 patients with primary SGTs including salivary ductal carcinoma (SDC), adenoid cystic carcinoma (AdCC), acinic cell carcinoma (ACC), mucoepidermoid carcinoma (MEC), warthin's tumors (WT), poleomorphic adenoma (PA) and other subtypes.
RESULTS: The expression of PD-1 in peripheral and central immune cells (ICs) of MEC, and peripheral ICs of ACC was significantly higher than those with AdCC (P = 0.02, P = 0.02, P = 0.03, respectively). Interestingly, the expression of PD-1 was also observed in peripheral and central malignant tumor cells (TCs), particularly in SDC and ACC. Despite no significant difference in PD-L1 expression of TCs among malignant subtypes, the peripheral and central ICs of ACC and MEC were revealed to express PDL-1 significantly more than those with AdCC (P < 0.05). WTs were rich in PD-1/PD-L1 expressing ICs. However, the tumor microenvironment of PA generally had low levels of PD-1/PD-L1 expression. In general, the expression of PD-1 in peripheral and central TCs was found to be significantly higher in malignant tumors than in benign ones (P = 0.002 and P = 0.003, respectively).
CONCLUSION: The simultaneous presentation of PD-1 and PD-L1 in TCs and ICs of SGTs, their significant association with disease severity as well as the positive correlation between these immune checkpoints may suggest the therapeutic potential of anti-PD-1 and anti-PDL-1 combinational immunotherapy for SGTs.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Immune check point; Immunohistochemistry; PD-1; PD-L1; Salivary gland tumor

Year:  2022        PMID: 36169795     DOI: 10.1007/s12105-022-01486-x

Source DB:  PubMed          Journal:  Head Neck Pathol        ISSN: 1936-055X


  43 in total

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Review 3.  Classification of Salivary Gland Neoplasms.

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4.  Association of Adjuvant Chemoradiotherapy vs Radiotherapy Alone With Survival in Patients With Resected Major Salivary Gland Carcinoma: Data From the National Cancer Data Base.

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Journal:  JAMA Otolaryngol Head Neck Surg       Date:  2016-11-01       Impact factor: 6.223

Review 5.  A Review of Selected Factors of Salivary Gland Tumour Formation and Malignant Transformation.

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7.  The Epidemiology of Salivary Glands Pathologies in Adult Population over 10 Years in Poland-Cohort Study.

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8.  Genomic landscape of salivary gland tumors.

Authors:  Shumei Kato; Sheryl K Elkin; Maria Schwaederle; Brett N Tomson; Teresa Helsten; Jennifer L Carter; Razelle Kurzrock
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9.  Comprehensive genomic profiles of metastatic and relapsed salivary gland carcinomas are associated with tumor type and reveal new routes to targeted therapies.

Authors:  J S Ross; L M Gay; K Wang; J A Vergilio; J Suh; S Ramkissoon; H Somerset; J M Johnson; J Russell; S Ali; A B Schrock; D Fabrizio; G Frampton; V Miller; P J Stephens; J A Elvin; D W Bowles
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Review 10.  A guide to cancer immunotherapy: from T cell basic science to clinical practice.

Authors:  Alex D Waldman; Jill M Fritz; Michael J Lenardo
Journal:  Nat Rev Immunol       Date:  2020-05-20       Impact factor: 53.106

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