Antigen processing and presentation‐related signature‐derived BNIP3 is a novel oncogene and immunotherapy determinant in osteosarcoma based on machine learning and in vitro validation

Author:

Chen Yang1,Cao Yajie2,Wu Song1,Cao Xu1,Cai Ting3,Hu Hai1

Affiliation:

1. Department of Orthopedics, The Third Xiangya Hospital Central South University Changsha China

2. Center of Clinical Pharmacology, The Third Xiangya Hospital Central South University Changsha China

3. Department of Gastroenterology, The Third Xiangya Hospital Central South University Changsha China

Abstract

AbstractBackgroundIn recent decades, osteosarcoma has remained the most prevalent kind of malignant tumor. An important and crucial factor in immunotherapy is antigen processing and presentation (APP). The specific functions and pathogenic processes of APP in osteosarcoma have not, however, been studied.MethodsPatients with osteosarcoma were divided into groups using APP‐related genes. Machine learning was used to further build the APP‐related score. Investigated in‐depth were the prognostic relevance of the score, mutation features, immunological aspects, and pharmacological prediction performance. Investigations of the prognostic utility, immunological traits, drug prediction effectiveness and immunotherapy prediction of BNIP3 were performed in‐depth.ResultsInvestigations by cell counting kit‐8, Transwell and 5‐ethynyl‐2‐deoxyuridine (EdU) demonstrated that BNIP3 is an osteosarcoma tumor accelerator. The osteosarcoma gene BNIP3 may promote macrophage migration. The APP‐related score shows potential for clinical use.ConclusionsIt was anticipated that more in vitro and in vivo studies would confirm BNIP3’s tumorigenic and immunogenic processes in osteosarcoma.

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

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