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Characteristics of m(6)A-related LncRNAs in breast cancer as prognostic biomarkers and immunotherapy

N6-methyladenosine (m(6)A) is a common RNA modification in coding and non-coding RNAs and plays an important role in the occurrence and development of breast cancer (BC). However, the role of m(6)A-related lncRNAs in breast cancer prognosis is unclear. This study aimed to help verify the biological...

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Detalles Bibliográficos
Autores principales: Han, Xinwei, Chen, Yu, Xie, Jiaogui, Wang, Yichao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539557/
https://www.ncbi.nlm.nih.gov/pubmed/37781080
http://dx.doi.org/10.7150/jca.87079
Descripción
Sumario:N6-methyladenosine (m(6)A) is a common RNA modification in coding and non-coding RNAs and plays an important role in the occurrence and development of breast cancer (BC). However, the role of m(6)A-related lncRNAs in breast cancer prognosis is unclear. This study aimed to help verify the biological function of m(6)A-related lncRNAs in breast cancer prognosis through bio-informatics techniques. First, we screened 18 m(6)A-related lncRNAs from the TCGA database: AL137847.1, AC137932.2, OTUD6B-AS1, MORF4L2-AS1, AC078846.1, AC012442.1, AL118556.1, AL138955.1, AC009754.1, AC024257.4, AL391095.1, AC024270.3, AC087392.1, LINC02649, AC090948.2, AL158212.1, ITGA6-AS1, AL133243.2 and constructed a risk-prognosis model based on this. Based on the model's median risk score, BC patients were divided into high-risk and low-risk groups. Then, the predictive value of the model was verified by Cox regression, Lasso regression, Kaplan-Meier curve and ROC curve analysis, and biological differences between the two groups were verified by GO enrichment analysis, tumor mutation burden, immune indications and in vitro tests. Importantly, the risk score of this prognostic model is an excellent independent prognostic factor, and m(6)A regulators are differentially expressed in patients with different risks. In addition, based on patients' different sensitivities to drugs, some drug candidates for different risk populations are screened to provide targets for breast cancer treatment. The difference in immune function between high-risk and low-risk patients also affected the sensitivity to immunotherapy. In the validation of clinical samples, we analyzed the expression of relevant lncRNAs in different risk groups and speculated the possible impact on the prognosis of breast cancer patients. The risk assessment tool built based on the full analysis of these m(6)A-related genes and m(6)A-related lncRNA libraries, as well as the m(6)A-related lncRNAs, has a high prognostic prediction ability, which may provide a supplementary screening method for accurately judging the prognosis of BC and a new perspective for personalized treatment of breast cancer patients.