Department of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China; Chongqing Key Laboratory of Molecular Oncology and Epigenetics, Chongqing, China.
Department of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Cell Signal. 2024 Oct;122:111337. doi: 10.1016/j.cellsig.2024.111337. Epub 2024 Aug 8.
Gemcitabine resistance is one of the leading causes of bladder cancer (BCa) recurrence and progression. The dysregulation of ferroptosis is involved in this process; however, the underlying mechanisms remain unclear. In the current study, we found a prominent increase in long non-coding RNA (lncRNA) small nucleolar RNA host gene 16 (SNHG16) in tumor samples, which was related to advanced tumor grade and poor prognosis. SNHG16 is overexpressed in the starving tumor microenvironment (STME) and induces gemcitabine resistance by inhibiting ferroptosis in BCa. SNHG16 knockdown promotes ferroptosis and increases chemosensitivity to gemcitabine. Mechanistically, the transcription factor MEF2A was markedly upregulated in the STME, facilitating SNHG16 expression. SNHG16 acts as a competing endogenous RNA that sponges miR-425-5p and promotes NOTCH2 expression. SNHG16/miR-425-5p/NOTCH2 is demonstrated, for the first time, to suppress ferroptosis by inducing SLC7A11 and GPX4 expression in vitro and in vivo. Upregulation of miR-425-5p reverses NOTCH2-mediated inhibition of ferroptosis, thereby mitigating gemcitabine resistance. In conclusion, these findings reveal that the STME-activated MEF2A/SNHG16/miR-425-5p/NOTCH2 axis induces gemcitabine resistance by inhibiting ferroptosis and implicate SNHG16 as a potential therapeutic target for chemoresistance.
吉西他滨耐药是膀胱癌(BCa)复发和进展的主要原因之一。铁死亡的失调参与了这个过程;然而,潜在的机制尚不清楚。在本研究中,我们发现在肿瘤样本中长链非编码 RNA(lncRNA)小核仁 RNA 宿主基因 16(SNHG16)显著增加,这与晚期肿瘤分级和预后不良有关。SNHG16 在饥饿肿瘤微环境(STME)中过度表达,并通过抑制 BCa 中的铁死亡诱导吉西他滨耐药。SNHG16 敲低促进铁死亡并增加吉西他滨的化疗敏感性。从机制上讲,转录因子 MEF2A 在 STME 中明显上调,促进 SNHG16 表达。SNHG16 作为一种竞争性内源性 RNA,可吸附 miR-425-5p 并促进 NOTCH2 表达。首次证明 SNHG16/miR-425-5p/NOTCH2 通过诱导 SLC7A11 和 GPX4 的表达在体外和体内抑制铁死亡。miR-425-5p 的上调逆转了 NOTCH2 介导的铁死亡抑制,从而减轻了吉西他滨耐药性。总之,这些发现表明 STME 激活的 MEF2A/SNHG16/miR-425-5p/NOTCH2 轴通过抑制铁死亡诱导吉西他滨耐药,并暗示 SNHG16 是化学耐药性的潜在治疗靶点。