PMID- 33817711 OWN - NLM STAT- MEDLINE DCOM- 20211028 LR - 20220531 IS - 2066-8279 (Electronic) IS - 1220-0522 (Print) IS - 1220-0522 (Linking) VI - 61 IP - 3 DP - 2020 Jul-Sep TI - Different patterns of p16INK4a immunohistochemical expression and their biological implications in laryngeal squamous cell carcinoma. PG - 697-706 LID - 10.47162/RJME.61.3.08 [doi] AB - INTRODUCTION: p16INK4a immunohistochemistry (IHC) is widely used to facilitate the diagnosis of human papillomavirus (HPV)-associated neoplasia, when >/=70% of cells show strong nuclear and cytoplasmic positivity. In this study, we aim to compare partial expression patterns that do not fulfill the above criteria and seek biological implications in laryngeal squamous cell carcinoma (LSCC). MATERIALS AND METHODS: p16INK4a IHC staining was conducted on representative sections of archived tissue from 88 LSCCs. Immunoreactivity was described based on four parameters: intracellular localization of immunostaining, intensity of immunostaining, distribution pattern and percentage of positive cells. RESULTS: Six patterns of p16INK4a immunoexpression were observed and defined as: strong diffuse (strong immunostaining, expression in cytoplasm and nucleus in >70% of tumor cells), weak diffuse (moderate or weak immunostaining, expression in cytoplasm in >70% of tumor cells), marginal (strong cytoplasmic immunostaining, limited to the periphery of tumor islets), strong scattered (strong immunostaining, expression in cytoplasm and nucleus in <50% of tumor cells), weak scattered (moderate or weak immunostaining, expression in cytoplasm in <50% of tumor cells), negative (no expression). The pN stage of the patients was associated with p16INK4a immunoexpression patterns, the marginal pattern was only found in the pN0-Nx stages, while the weak diffuse pattern was more frequently observed in pN2-N3 stages. CONCLUSIONS: Partial immunostaining with architecturally distinct p16INK4a immunoexpression patterns may prove significant in stratifying characteristic clinicopathological subgroups among LSCC. Our observations may support the hypothesis that p16INK4a has different roles in different subcellular locations, with tumorigenic molecular pathways unrelated to HPV infection. FAU - Lazar, Camelia Sidonia AU - Lazar CS AD - Discipline of Histology, Department of Morphological Sciences, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania; a_sovrea@yahoo.com. FAU - Sovrea, Alina Simona AU - Sovrea AS FAU - Georgiu, Carmen AU - Georgiu C FAU - Crisan, Doinita AU - Crisan D FAU - Mirescu, Stefan Claudiu AU - Mirescu SC FAU - Cosgarea, Marcel AU - Cosgarea M LA - eng PT - Journal Article PL - Romania TA - Rom J Morphol Embryol JT - Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie JID - 9112454 RN - 0 (Biomarkers, Tumor) RN - 0 (Cyclin-Dependent Kinase Inhibitor p16) SB - IM MH - Biomarkers, Tumor MH - *Carcinoma, Squamous Cell MH - Cyclin-Dependent Kinase Inhibitor p16 MH - Female MH - *Head and Neck Neoplasms MH - Humans MH - Papillomaviridae MH - Squamous Cell Carcinoma of Head and Neck MH - *Uterine Cervical Neoplasms PMC - PMC8112783 COIS- The authors declare that they have no conflict of interests. EDAT- 2021/04/06 06:00 MHDA- 2021/10/29 06:00 PMCR- 2020/07/01 CRDT- 2021/04/05 06:20 PHST- 2021/04/05 06:20 [entrez] PHST- 2021/04/06 06:00 [pubmed] PHST- 2021/10/29 06:00 [medline] PHST- 2020/07/01 00:00 [pmc-release] AID - 610320697706 [pii] AID - 10.47162/RJME.61.3.08 [doi] PST - ppublish SO - Rom J Morphol Embryol. 2020 Jul-Sep;61(3):697-706. doi: 10.47162/RJME.61.3.08.