A novel autophagy-related lncRNA prognostic risk model for breast cancer.
A novel autophagy-related lncRNA prognostic risk model for breast cancer.
复制标题
DOI:
10.1111/jcmm.15980
复制
发表时间:
2021-01
影响因子:
5.3
通讯作者:
Li Y
中科院分区:
文献类型:
--
作者:
Li X;Jin F;Li Y
Long non‐coding RNAs (lncRNAs) are well known as crucial regulators to breast cancer development and are implicated in controlling autophagy. LncRNAs are also emerging as valuable prognostic factors for breast cancer patients. It is critical to identify autophagy‐related lncRNAs with prognostic value in breast cancer. In this study, we identified autophagy‐related lncRNAs in breast cancer by constructing a co‐expression network of autophagy‐related mRNAs‐lncRNAs from The Cancer Genome Atlas (TCGA). We evaluated the prognostic value of these autophagy‐related lncRNAs by univariate and multivariate Cox proportional hazards analyses and eventually obtained a prognostic risk model consisting of 11 autophagy‐related lncRNAs (U62317.4, LINC01016, LINC02166, C6orf99, LINC00992, BAIAP2‐DT, AC245297.3, AC090912.1, Z68871.1, LINC00578 and LINC01871). The risk model was further validated as a novel independent prognostic factor for breast cancer patients based on the calculated risk score by Kaplan‐Meier analysis, univariate and multivariate Cox regression analyses and time‐dependent receiver operating characteristic (ROC) curve analysis. Moreover, based on the risk model, the low‐risk and high‐risk groups displayed different autophagy and oncogenic statues by principal component analysis (PCA) and Gene Set Enrichment Analysis (GSEA) functional annotation. Taken together, these findings suggested that the risk model of the 11 autophagy‐related lncRNAs has significant prognostic value for breast cancer and might be autophagy‐related therapeutic targets in clinical practice.
登录
查看更多内容
DOI:
10.1146/annurev-cancerbio-041816-122338
发表时间:
2017-01-01
期刊:
ANNUAL REVIEW OF CANCER BIOLOGY, VOL 1
影响因子:
--
作者:
Santana-Codina, Naiara;Mancias, Joseph D.;Kimmelman, Alec C.
通讯作者:
Kimmelman, Alec C.
影响因子:
13.3
作者:
Chang, Chia-Hao;Bijian, Krikor;Alaoui-Jamali, Moulay A.
通讯作者:
Alaoui-Jamali, Moulay A.
影响因子:
21.3
作者:
Liu X;Xiao ZD;Han L;Zhang J;Lee SW;Wang W;Lee H;Zhuang L;Chen J;Lin HK;Wang J;Liang H;Gan B
通讯作者:
Gan B
DOI:
10.1093/annonc/mdt303
发表时间:
2013-09
期刊:
Annals of oncology : official journal of the European Society for Medical Oncology
影响因子:
--
作者:
Goldhirsch A;Winer EP;Coates AS;Gelber RD;Piccart-Gebhart M;Thürlimann B;Senn HJ;Panel members
通讯作者:
Panel members
影响因子:
30.8
作者:
Kim J;Piao HL;Kim BJ;Yao F;Han Z;Wang Y;Xiao Z;Siverly AN;Lawhon SE;Ton BN;Lee H;Zhou Z;Gan B;Nakagawa S;Ellis MJ;Liang H;Hung MC;You MJ;Sun Y;Ma L
通讯作者:
Ma L