Abstract
Background:
Glypican-3 (GPC3), a cell surface glycoprotein, regulates cell growth and exhibits increased expression in hepatocellular carcinoma (HCC) and squamous non-small cell lung cancer (SQ-NSCLC). This study developed an artificial intelligence (AI) algorithm for predicting GPC3 expression to accelerate clinical trial enrollment, comparing it with manual immunohistochemistry (IHC) scoring.
Methods:
Using 167 NSCLC and 133 HCC formalin-fixed paraffin-embedded tumor blocks, GPC3 expression was quantified via IHC assays. Machine learning (ML) models were trained on digitized NSCLC whole slide images to identify GPC3-positive tumor areas, applying data-driven cutoffs for classification. Association between GPC3 and programmed cell death-ligand 1 (PD-L1) IHC expression in NSCLC sample was explored.
Results:
GPC3 expression peaked in HCC (63.9%), followed by SQ-NSCLC (52.6%) and adeno-NSCLC (lung adenocarcinoma) (10.0%). No significant correlation was found between GPC3 and PD-L1 expression in SQ-NSCLC. AI-based screening surpassed clinical pathologists by 10% in precision, achieving 100% recall at a 1% cutoff. ML model quantification aligned well with pathologist consensus. Profiling GPC3 expression emphasized its prevalence in HCC and SQ-NSCLC.
Conclusion:
Our AI platform standardizes, scales, and reproducibly characterizes GPC3 in NSCLC, supporting patient selection in clinical studies.
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
