AIM-CICs: an automatic identification method for cell-in-cell structures based on convolutional neural network

Author:

Tang Meng123,Su Yan2,Zhao Wei4,Niu Zubiao2,Ruan Banzhan2,Li Qinqin1,Zheng You2,Wang Chenxi2,Zhang Bo12,Zhou Fuxiang5,Wang Xiaoning6,Huang Hongyan1,Shi Hanping1,Sun Qiang2ORCID

Affiliation:

1. Beijing Shijitan Hospital of Capital Medical University , Beijing 100038 , China

2. Laboratory of Cell Engineering, Institute of Biotechnology, Research Unit of Cell Death Mechanism, Chinese Academy of Medical Science , 2021RU008, Beijing 100071 , China

3. Comprehensive Oncology Department, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing 100021 , China

4. School of Mathematical Sciences, Peking University , Beijing 100871 , China

5. Department of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Clinical Cancer Study Center, Zhongnan Hospital, Wuhan University , Wuhan 430071 , China

6. National Clinic Center of Geriatric & State Key Laboratory of Kidney, Chinese PLA General Hospital , Beijing 100853 , China

Abstract

ABSTRACT Whereas biochemical markers are available for most types of cell death, current studies on non-autonomous cell death by entosis rely strictly on the identification of cell-in-cell structures (CICs), a unique morphological readout that can only be quantified manually at present. Moreover, the manual CIC quantification is generally over-simplified as CIC counts, which represents a major hurdle against profound mechanistic investigations. In this study, we take advantage of artificial intelligence technology to develop an automatic identification method for CICs (AIM-CICs), which performs comprehensive CIC analysis in an automated and efficient way. The AIM-CICs, developed on the algorithm of convolutional neural network, can not only differentiate between CICs and non-CICs (the area under the receiver operating characteristic curve (AUC) > 0.99), but also accurately categorize CICs into five subclasses based on CIC stages and cell number involved (AUC > 0.97 for all subclasses). The application of AIM-CICs would systemically fuel research on CIC-mediated cell death, such as high-throughput screening.

Funder

Beijing Municipal Natural Science Foundation

National Key Research and Development of China

National Natural Science Foundation of China

Beijing Municipal Administration of Hospitals

Beijing Postdoctoral Research Foundation

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

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