“…LINC01426 modulates CTBP1/miR-423-5p/FOXM1 axis via interacting with IGF2BP1 to aggravate ccRCC progression ( Jiang et al, 2021b ), it also aggravates the malignant progression through miR-661/Mdm2 axis in glioma ( Shu et al, 2022 ), it serves as a prognostic indicator in lung adenocarcinoma by triggering growth and metastasis ( Deng et al, 2022 ), what’s more, in a recently reported study on ferroptosis-related lncRNAs of glioma, LINC01426 was identified to be related to ferroptosis, its knockdown could significantly increase in the Fe 2+ levels and the erastin-induced ROS levels in glioma cells ( Huang et al, 2022 ). LncRNA DUXAP8 acts as an oncogene in most tumors, its abnormal overexpression is associated with the proliferation, invasion, migration, anti-autophagy, and poor prognosis of tumors ( Wang et al, 2022a ; Wang et al, 2022b ), it may act as a potential therapeutic target for cancer ( Wang et al, 2022b ); in a research on identification of necroptosis-related lncRNAs in hepatocellular carcinoma, DUXAP8 was identified as a prognostic lncRNA and related to patients’ prognosis ( Chen et al, 2022b ); In addition to our research, other studies have also found that it is involved in the process of ferroptosis in tumor, such as: it can act with ferroptosis-associated gene FANCD2 to form DUXAP8-miR-29c-FANCD2 axe in hepatocellular carcinoma ( Yang et al, 2022 ), it was also identified as one of ferroptosis-related lncRNAs in kidney carcinoma ( Xing et al, 2021 ). Similar to DUXAP8, lncRNA PVT1 was considered as involved in the ferroptosis progress, it may regulate ferroptosis through miR-214-mediated TFR1 and TP53 expression ( Lu, Xu & Lu, 2020 ), it was identified as one of the ferroptosis-related lncRNAs to construct a panel for predicting tumor progression, microenvironment ( He et al, 2021 ), and radiotherapy response ( Zheng et al, 2021 ) in glioma; in liver cancer, PVT1 is involved in the regulatory mechanism of lncPVT1/miR-214-3p/GPX4 axis and plays a role in ketamine suppressing the viability of liver cancer cells and inducing ferroptosis.…”