期刊
FREE RADICAL BIOLOGY AND MEDICINE
卷 168, 期 -, 页码 25-43出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2021.03.023
关键词
m(6)A RNA methylation; METTL3; SLC3A2; RNA stability; HOXA13; Transcriptional regulation
资金
- National Natural Science Foundation of China [81871907, 81822029, 81672332, 81902315, 81902869, 81774291]
- Shanghai Municipal Education Commission-Gaofeng Clinical Medicine [20191834]
- Project of Clinical Research Supporting System, Clinical Medicine First-class Discipline, Shanghai Rising Star Program [18QA1403400]
- Shanghai Municipal Commission of Health and Family Planning [2017YQ024]
- Grant Support Chen Guang project - Shanghai Municipal Education Commission
- Grant Support Chen Guang project - Shanghai Education Development Foundation [18CG16]
- Shanghai Sailing Program [19YF1444800]
- Nurture projects for basic research of Shanghai Chest Hospital [2018YNJCQ06, 2018YNJCM01]
YTHDC2 induces ferroptosis in LUAD cells by inhibiting HOXA13 to suppress SLC3A2, along with SLC7A11, which are crucial for tumor growth inhibition and lipid peroxidation induced by YTHDC2.
The m(6)A reader YT521-B homology containing 2 (YTHDC2) has been identified to inhibit lung adenocarcinoma (LUAD) tumorigenesis by suppressing solute carrier 7A11 (SLC7A11)-dependent antioxidant function. SLC7A11 is a major functional subunit of system X-C(-). Inhibition of system X-C(-) can induce ferroptosis. However, whether suppressing SLC7A11 is sufficient for YTHDC2 to be an endogenous ferroptosis inducer in LUAD is unknown. Here, we found that induction of YTHDC2 to a high level can induce ferroptosis in LUAD cells but not in lung and bronchus epithelial cells. In addition to SLC7A11, solute carrier 3A2 (SLC3A2), another subunit of system X-C(-) was equally important for YTHDC2-induced ferroptosis. YTHDC2 m(6)A-dependently destabilized Homeo box A13 (HOXA13) mRNA because a potential m(6)A recognition site was identified within its 3' untranslated region (3'UTR). Interestingly, HOXA13 acted as a transcription factor to stimulate SLC3A2 expression. Thereby, YTHDC2 suppressed SLC3A2 via inhibiting HOXA13 in an m(6)A-indirect manner. Mouse experiments further confirmed the associations among YTHDC2, SLC3A2 and HOXA13, and demonstrated that SLC3A2 and SLC7A11 were both important for YTHDC2-impaired tumor growth and -induced lipid peroxidation in vivo. Moreover, higher expression of SLC7A11, SLC3A2 and HOXA13 indicate poorer clinical outcome in YTHDC2-suppressed LUAD patients. In conclusion, YTHDC2 is believed to be a powerful endogenous ferroptosis inducer and targeting SLC3A2 subunit of system X-C(-) is essential for this process. Increasing YTHDC2 is an alternative ferroptosis-based therapy to treat LUAD.
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