Abstract

Abstract The reprogramming of cellular metabolism to support continuous proliferation is a hallmark of cancer. Accumulating evidence indicates that the reprogramming of tumor metabolism is under the control of various oncogenic signals. The KRAS oncogene is known to induce aerobic glycolysis, and pancreatic adenocarcinoma (PDAC) cells have been shown previously to have metabolism consistent with elevated aerobic glycolysis. Survival analysis showed that higher glycolysis activity was associated with worse clinical outcome in TCGA PDAC. Several glycolytic inhibitors are currently in preclinical and clinical development. It had been reported that cancer metabolic status could play a role in the interaction with tumor microenvironment. We hypothesized that cancer glycolysis activity could affect tumor histopathological architecture in PDAC. As a proof-of-concept study, we trained a deep learning convolutional neural network (CNN) model (Google Inception v3) on histopathological images obtained from TCGA PAAD cohort to classify tumors with high and low glycolysis pathway activity. We aimed to answer whether CNNs can predict PDAC glycolysis status using images as the only input. Our model was tested on separate tissue samples from the same cohort. Aggregated accuracy was 75% on 48 cases with area under ROC curve as 0.751. Prediction scores significantly correlated with transcriptome-based glycolysis signature (Pearson correlation = 0.352, p=0.007). The current study demonstrates the potential of deep learning approaches for histopathologically classifying cancer based on metabolic status. This information could be of value in assisting clinical decisions on targeting cancer metabolism. Citation Format: Peiling Tsou, Chang-Jiun Wu. Seeing glycolysis on PDAC: Applying deep learning convolutional neural network model [abstract]. In: Proceedings of the AACR Virtual Special Conference on Artificial Intelligence, Diagnosis, and Imaging; 2021 Jan 13-14. Philadelphia (PA): AACR; Clin Cancer Res 2021;27(5_Suppl):Abstract nr PO-016.

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