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Tumor-infiltrating macrophage associated lncRNA signature in cutaneous melanoma: implications for diagnosis, prognosis, and immunotherapy.
Wan, Qi; Deng, Yuhua; Wei, Ran; Ma, Ke; Tang, Jing; Deng, Ying-Ping.
Affiliation
  • Wan Q; Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Deng Y; Department of Infection Control, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Wei R; Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Ma K; Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Tang J; Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
  • Deng YP; Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Aging (Albany NY) ; 16(5): 4518-4540, 2024 03 13.
Article in En | MEDLINE | ID: mdl-38475660
ABSTRACT
Along with the increasing knowledge of long noncoding RNA, the interaction between the long noncoding RNA (lncRNA) and tumor immune infiltration is increasingly valued. However, there is a lack of understanding of correlation between regulation of specific lncRNAs and tumor-infiltrating macrophages within melanoma. In this research, a macrophage associated lncRNA signature was identified by multiple machine learning algorithms and the robust and effectiveness of signature also validated in other independent datasets. The signature contained six specific lncRNAs (PART1, LINC00968, LINC00954, LINC00944, LINC00518 and C20orf197) was constructed, which could diagnose melanoma and predict the prognosis of patients. Moreover, our signature achieves higher accuracy than the previous well-established markers and regarded as an independent prognostic indicator. The pathway enrichment revealed that these lncRNAs were closely correlated with many immune processes. In addition, the signature was associated with different immune microenvironment and applied to predict response of immune checkpoint inhibitor therapy (low risk of patients well respond to anti-PD-1 therapy and high risk is insensitive to anti-CTLA-4 therapy). Therefore, our finding supplies a more accuracy and effective lncRNA signature for tumor-infiltrating macrophages targeting treatment approaches and affords a new clinical application for predicting the response of immunotherapies in melanomas.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / RNA, Long Noncoding / Melanoma Limits: Humans Language: En Journal: Aging (Albany NY) Journal subject: GERIATRIA Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / RNA, Long Noncoding / Melanoma Limits: Humans Language: En Journal: Aging (Albany NY) Journal subject: GERIATRIA Year: 2024 Document type: Article Affiliation country: China