Machine Learning Classifies Ferroptosis and Apoptosis Cell Death Modalities with TfR1 Immunostaining.


Journal

ACS chemical biology
ISSN: 1554-8937
Titre abrégé: ACS Chem Biol
Pays: United States
ID NLM: 101282906

Informations de publication

Date de publication:
18 03 2022
Historique:
pubmed: 2 3 2022
medline: 30 4 2022
entrez: 1 3 2022
Statut: ppublish

Résumé

Determining cell death mechanisms occurring in patient and animal tissues is a longstanding goal that requires suitable biomarkers and accurate quantification. However, effective methods remain elusive. To develop more powerful and unbiased analytic frameworks, we developed a machine learning approach for automated cell death classification. Image sets were collected of HT-1080 fibrosarcoma cells undergoing ferroptosis or apoptosis and stained with an anti-transferrin receptor 1 (TfR1) antibody, together with nuclear and F-actin staining. Features were extracted using high-content-analysis software, and a classifier was constructed by fitting a multinomial logistic lasso regression model to the data. The prediction accuracy of the classifier within three classes (control, ferroptosis, apoptosis) was 93%. Thus, TfR1 staining, combined with nuclear and F-actin staining, can reliably detect both apoptotic and ferroptotis cells when cell features are analyzed in an unbiased manner using machine learning, providing a method for unbiased analysis of modes of cell death.

Identifiants

pubmed: 35230809
doi: 10.1021/acschembio.1c00953
pmc: PMC8938922
doi:

Substances chimiques

Actins 0
Biomarkers 0
Receptors, Transferrin 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

654-660

Subventions

Organisme : NCI NIH HHS
ID : R35 CA209896
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA087497
Pays : United States
Organisme : NCI NIH HHS
ID : UG3 CA256962
Pays : United States
Organisme : NINDS NIH HHS
ID : R33 NS109407
Pays : United States
Organisme : NINDS NIH HHS
ID : R61 NS109407
Pays : United States

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Auteurs

Jenny Jin (J)

Department of Biological Sciences, Columbia University, New York, New York 10027, United States.
Department of Chemistry, Columbia University, New York, New York 10027, United States.

Kenji Schorpp (K)

HelmholtzZentrum München, German Research Center for Environmental Health, Cell Signaling and Chemical Biology, Institute for Molecular Toxicology and Pharmacology, 85764 Neuherberg, Germany.

Daniel Samaga (D)

HelmholtzZentrum München, German Research Center for Environmental Health, Research Unit Radiation Cytogenetics, 85764 Neuherberg, Germany.

Kristian Unger (K)

HelmholtzZentrum München, German Research Center for Environmental Health, Research Unit Radiation Cytogenetics, 85764 Neuherberg, Germany.

Kamyar Hadian (K)

HelmholtzZentrum München, German Research Center for Environmental Health, Cell Signaling and Chemical Biology, Institute for Molecular Toxicology and Pharmacology, 85764 Neuherberg, Germany.

Brent R Stockwell (BR)

Department of Biological Sciences, Columbia University, New York, New York 10027, United States.
Department of Chemistry, Columbia University, New York, New York 10027, United States.
Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York 10032, United States.
Irving Institute for Cancer Dynamics, Columbia University, New York, New York 10027, United States.

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Classifications MeSH