ǂa ǂphenotype with distinct immune microenvironment
Abstract
Introduction: The CDKN2A gene plays a central role in the pathogenesis of malignant pleural mesothelioma (MPM). The gene encodes for two tumor suppressor proteins, p16/INK4A and p14/ARF, frequently lost in MPM tumors. The exact role of p14/ARF in MPM and overall its correlation with the immune microenvironment is unknown. We aimed to determine whether there is a relationship between p14/ARF expression, tumor morphological features, and the inflammatory tumor microenvironment. Methods: Diagnostic biopsies from 76 chemo-naive MPMs were evaluated. Pathological assessments of histotype, necrosis, inflammation, grading, and mitosis were performed. We evaluated p14/ARF, PD-L1 (tumor proportion score, TPS), and Ki-67 (percentage) by immunohistochemistry. Inflammatory cell components (CD3+, CD4+, CD8+ T lymphocytes; CD20+ B-lymphocytes; CD68+ and CD163+ macrophages) were quantified as percentages of positive cells, distinguishing between intratumoral and peritumoral areas. The expression of p14/ARF was associated with several clinical and pathological characteristics. A random forest-based machine-learning algorithm (Boruta) was implemented to identify which variables were associated with p14/ARF expression. Results: p14/ARF was evaluated in 68 patients who had a sufficient number of tumor cells. Strong positivity was detected in 14 patients (21%) (11 epithelioid and 3 biphasic MPMs). At univariate analysis, p14/ARF-positive epithelioid mesotheliomas showed higher nuclear grade (G3) (p = 0.023) and higher PD-L1 expression (≥50%) (p = 0.042). The percentages of CD4 and CD163 in peritumoral areas were respectively higher and lower in p14/ARF positive tumors but did not reach statistical significance with our sample size (both p = 0.066). The Boruta algorithm confirmed the predictive value of PD-L1 percentage for p14/ARF expression in all histotypes. Conclusions: p14/ARF-positive epithelioid mesotheliomas may mark a more aggressive pathological phenotype (higher nuclear grade and PD-L1 expression). Considering the results regarding the tumor immune microenvironment, p14/ARF-negative tumors seem to have an immune microenvironment less sensitive to immune checkpoint inhibitors, being associated with low PD-L1 and CD4 expression, and high CD163 percentage. The association between p14/ARF-positive MPMs and PD-L1 expression suggests a possible interaction of the two pathways. Confirmation of our preliminary results could be important for patient selection and recruitment in future clinical trials with anticancer immunotherapy.
Keywords
maligni plevralni mezoteliom;malignant pleural mesothelioma;
Data
Language: |
English |
Year of publishing: |
2022 |
Typology: |
1.01 - Original Scientific Article |
Publisher: |
Frontiers |
UDC: |
616 |
COBISS: |
103281667
|
ISSN: |
2234-943X |
Views: |
116 |
Downloads: |
88 |
Average score: |
0 (0 votes) |
Metadata: |
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Other data
Secondary keywords: |
Neoplasms;Lung;Pathology;Cytology;Mesothelioma, malignant;Tumor microenvironment;Novotvorbe;Pljuča;Patologija;Citologija;Maligni mezoteliom;Tumorsko mikrookolje; |
Source comment: |
Nasl. z nasl. zaslona;
Soavtorja iz Slovenije: Izidor Kern, Gregor Vlačić;
Opis vira z dne 4. 4. 2022;
|
Pages: |
str. 30-39 |
Issue: |
ǂVol. ǂ11 |
Chronology: |
22 Mar. 2022 |
DOI: |
10.3389/fonc.2021.653497 |
ID: |
15468537 |