PATZ1 in Non-Small Cell Lung Cancer: A New Biomarker That Negatively Correlates with PD-L1 Expression and Suppresses the Malignant Phenotype

Author:

Lucà Stefano1,Franco Renato1,Napolitano Antonella2,Soria Valeria2,Ronchi Andrea1,Zito Marino Federica1,Della Corte Carminia Maria3,Morgillo Floriana3,Fiorelli Alfonso4ORCID,Luciano Antonio5,Palma Giuseppe5ORCID,Arra Claudio5,Battista Sabrina2ORCID,Cerchia Laura2ORCID,Fedele Monica2ORCID

Affiliation:

1. Pathology Unit, Department of Mental and Physical Health and Preventive Medicine, University of Campania “Luigi Vanvitelli”, 80138 Naples, Italy

2. Institute for Experimental Endocrinology and Oncology (IEOS), National Research Council (CNR), 80145 Naples, Italy

3. Department of Precision Medicine, Medical Oncology, University of Campania “Luigi Vanvitelli”, 80138 Naples, Italy

4. Translational Medical and Surgical Science, Thoracic Surgery, University of Campania “Luigi Vanvitelli”, 80138 Naples, Italy

5. S.S.D. Sperimentazione Animale, Istituto Nazionale Tumori—IRCCS—Fondazione G. Pascale, 80131 Naples, Italy

Abstract

Non-small cell lung cancer (NSCLC), the leading cause of cancer death worldwide, is still an unmet medical problem due to the lack of both effective therapies against advanced stages and markers to allow a diagnosis of the disease at early stages before its progression. Immunotherapy targeting the PD-1/PD-L1 checkpoint is promising for many cancers, including NSCLC, but its success depends on the tumor expression of PD-L1. PATZ1 is an emerging cancer-related transcriptional regulator and diagnostic/prognostic biomarker in different malignant tumors, but its role in lung cancer is still obscure. Here we investigated expression and role of PATZ1 in NSCLC, in correlation with NSCLC subtypes and PD-L1 expression. A cohort of 104 NSCLCs, including lung squamous cell carcinomas (LUSCs) and adenocarcinomas (LUADs), was retrospectively analyzed by immunohistochemistry for the expression of PATZ1 and PD-L1. The results were correlated with each other and with the clinical characteristics, showing on the one hand a positive correlation between the high expression of PATZ1 and the LUSC subtype and, on the other hand, a negative correlation between PATZ1 and PD-L1, validated at the mRNA level in independent NSCLC datasets. Consistently, two NSCLC cell lines transfected with a PATZ1-overexpressing plasmid showed PD-L1 downregulation, suggesting a role for PATZ1 in the negative regulation of PD-L1. We also showed that PATZ1 overexpression inhibits NSCLC cell proliferation, migration, and invasion, and that Patz1-knockout mice develop LUAD. Overall, this suggests that PATZ1 may act as a tumor suppressor in NSCLC.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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