4.7 Article

Artificial Intelligence-Based Tissue Phenotyping in Colorectal Cancer Histopathology Using Visual and Semantic Features Aggregation

期刊

MATHEMATICS
卷 10, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/math10111909

关键词

artificial intelligence; computational pathology; tumor microenvironment; colorectal cancer; cancer diagnosis

资金

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT (MSIT) through the Basic Science Research Program [NRF2021R1F1A1045587]
  2. NRF - MSIT through the Basic Science Research Program [NRF-2020R1A2C1006179]
  3. MSIT, Korea, under the ITRC (Information Technology Research Center) support program [IITP-2022-2020-0-01789]

向作者/读者索取更多资源

In this paper, a novel deep learning method is proposed for the detection and phenotyping of colorectal cancer tissue. The method achieves higher accuracy and efficiency compared to state-of-the-art methods by incorporating visual and semantic information and applying data augmentation techniques.
Tissue phenotyping of the tumor microenvironment has a decisive role in digital profiling of intra-tumor heterogeneity, epigenetics, and progression of cancer. Most of the existing methods for tissue phenotyping often rely on time-consuming and error-prone manual procedures. Recently, with the advent of advanced technologies, these procedures have been automated using artificial intelligence techniques. In this paper, a novel deep histology heterogeneous feature aggregation network (HHFA-Net) is proposed based on visual and semantic information fusion for the detection of tissue phenotypes in colorectal cancer (CRC). We adopted and tested various data augmentation techniques to avoid computationally expensive stain normalization procedures and handle limited and imbalanced data problems. Three publicly available datasets are used in the experiments: CRC tissue phenotyping (CRC-TP), CRC histology (CRCH), and colon cancer histology (CCH). The proposed HHFA-Net achieves higher accuracies than the state-of-the-art methods for tissue phenotyping in CRC histopathology images.

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