98%
921
2 minutes
20
Background: Small cell lung cancer (SCLC) is a highly aggressive neuroendocrine carcinoma (NEC) with poor prognosis due to chemotherapy resistance. Molecular subtypes, including ASCL1, NEUROD1, YAP1 and POU2F3, have distinct clinical implications. POU2F3, linked to a tuft cell-like lineage, represents a non-neuroendocrine subtype found in SCLC and extrapulmonary NECs. However, its prognostic and clinical significance remain unclear.
Methods: A meta-analysis was performed to assess the relationship between POU2F3 expression and clinical outcomes in SCLC and NECs. Studies reporting clinicopathological or survival data related to POU2F3 expression, identified immunohistochemistry, were included. This review was performed following the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and was registered on the International Prospective Register of Systematic Reviews (registration number: CRD42023478789).
Results: Sixteen studies involving 2011 patients met inclusion criteria. Pooled analysis revealed that POU2F3 expression in SCLC significantly improved OS (HR = 0.74, 95% CI = 0.61-0.90, < .01 and PFS/RFS (HR = 0.69, 95% CI = 0.53-0.90, < .01). Subgroup analyses associated POU2F3 positivity with favourable survival when surgical specimen or whole slide analysis was used, or when studies with chemotherapy regimen were included. POU2F3 expression also correlated with younger age ( = .02) and male sex ( = .03) but not with smoking history, tumour stage, nodal involvement, or vascular invasion.
Conclusion: POU2F3 expression is associated with improved survival and correlates with younger age and male sex in SCLC, highlighting distinct clinical and biological characteristics of this tuft cell-originated subtype. Data on extrapulmonary NECs were limited, precluding definitive conclusions for this population.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1080/07853890.2025.2556253 | DOI Listing |
Ann Med
December 2025
Department of Hospital Pathology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Background: Small cell lung cancer (SCLC) is a highly aggressive neuroendocrine carcinoma (NEC) with poor prognosis due to chemotherapy resistance. Molecular subtypes, including ASCL1, NEUROD1, YAP1 and POU2F3, have distinct clinical implications. POU2F3, linked to a tuft cell-like lineage, represents a non-neuroendocrine subtype found in SCLC and extrapulmonary NECs.
View Article and Find Full Text PDFLab Invest
September 2025
Department of Pathology and Clinical Bioinformatics, Erasmus MC, Rotterdam, The Netherlands. Electronic address:
Large-cell neuroendocrine carcinoma (LCNEC) can be genomically subtyped into small cell lung cancer (SCLC)- and non-SCLC (NSCLC)-like. NEUROD1, ASCL1, POU2F3, and YAP1 (NAPY) subtypes have been reported for SCLC. We immunohistochemically evaluated NAPY in LCNEC alongside relevant protein expression data.
View Article and Find Full Text PDFCell Tissue Res
September 2025
Institute for Anatomy and Cell Biology, German Center for Lung Research, Excellence Cluster Cardio-Pulmonary Institute (CPI), Justus Liebig University Giessen, 35392, Giessen, Germany.
Previous studies identified a rare cell type in the mouse tracheal epithelium with immunoreactivity to the microvillus protein villin (Vil1), which persisted in mice lacking tuft cells due to deletion of the transcription factor Pou2f3. This study aimed to clarify the identity of this ill-defined cell type. Ultrastructurally, all cells with tightly packed microvilli observed in the tracheal epithelium of Pou2f3-mice contained basally located dense core vesicles, a characteristic feature of neuroendocrine cells (NEC).
View Article and Find Full Text PDFLung Cancer
August 2025
Division of Thoracic Surgery, Keio University School of Medicine, Tokyo, Japan.
Introduction: Thymic neuroendocrine tumors (TNETs) are rare malignancies characterized by aggressive clinical behavior and limited therapeutic options. In small cell lung cancer (SCLC), molecular subtypes based on the expression of lineage-defining transcription factors (TFs)-ASCL1, NEUROD1, POU2F3, and YAP1-have been proposed. However, the TF landscape of TNETs remains poorly defined.
View Article and Find Full Text PDFJ Pathol
August 2025
Department of Molecular and Cellular Pathology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.
Small cell lung cancer (SCLC) is classified into distinct molecular subtypes based on the expression patterns of four transcription regulators: achaete-scute homolog 1 (ASCL1), neuronal differentiation 1 (NEUROD1), POU class 2 homeobox 3 (POU2F3), and yes-associated protein 1 (YAP1). MicroRNAs (miRNAs) play critical roles in cancer cellular processes but their subtype-specific implications in SCLC remain underexplored. Out of 46 surgically resected SCLC samples, miRNA visualization through in situ hybridization identified high expression of miR-375 in the ASCL1, NEUROD1, and ASCL1/NEUROD1 subtypes, and miR-9-5p in the POU2F3 subtype.
View Article and Find Full Text PDF