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<p>Glioblastoma (GBM) recurrence is driven by therapy-resistant cells that escape surgical detection and withstand subsequent chemoradiotherapy. However, the molecular basis connecting invasion, metabolic detectability, and treatment resistance remains elusive. Here, we identify Coronin-1A (Coro1A), a cytoplasmic actin-associated regulator, as a multidirectional modulator of cancer stemness in GBM. Across six patient-derived GBM lines, Coro1A mRNA expression strongly correlated with both cell motility and the proportion of 5-aminolevulinic acid (5-ALA)–negative cells, and high Coro1A levels predicted significantly poorer prognosis in recurrent GBM cases. To assess its function, Coro1A-knockdown clones were generated from a recurrent GBM–derived culture (PDM123). Silencing Coro1A significantly reduced migration and modestly decreased proliferation, with the extent of motility reduction correlating with residual Coro1A expression. Importantly, knockdown enhanced intracellular accumulation of protoporphyrin IX (PpIX) under 5-ALA treatment, even in highly motile cells, indicating that Coro1A simultaneously governs invasiveness and intraoperative fluorescence detectability. Furthermore, Coro1A depletion increased sensitivity to temozolomide (TMZ) and X-ray irradiation, revealing its critical contribution to therapy resistance. Collectively, these findings establish Coro1A as a central cytoskeletal regulator that unifies invasion, diagnostic escape, and therapeutic resilience—highlighting its potential as a curative target capable of dismantling the multifaceted resistance of GBM.</p>

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The cytoskeletal regulator Coronin-1A plays a multidirectional role in glioblastoma stemness

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月28日

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  • TingTing Zhang,
  • Ichiyo Shibahara,
  • Takuichiro Hide,
  • Toshihiro Kumabe,
  • Shun-Ichiro Ogura,
  • Tetsuya Taga,
  • Kouichi Tabu

摘要

Glioblastoma (GBM) recurrence is driven by therapy-resistant cells that escape surgical detection and withstand subsequent chemoradiotherapy. However, the molecular basis connecting invasion, metabolic detectability, and treatment resistance remains elusive. Here, we identify Coronin-1A (Coro1A), a cytoplasmic actin-associated regulator, as a multidirectional modulator of cancer stemness in GBM. Across six patient-derived GBM lines, Coro1A mRNA expression strongly correlated with both cell motility and the proportion of 5-aminolevulinic acid (5-ALA)–negative cells, and high Coro1A levels predicted significantly poorer prognosis in recurrent GBM cases. To assess its function, Coro1A-knockdown clones were generated from a recurrent GBM–derived culture (PDM123). Silencing Coro1A significantly reduced migration and modestly decreased proliferation, with the extent of motility reduction correlating with residual Coro1A expression. Importantly, knockdown enhanced intracellular accumulation of protoporphyrin IX (PpIX) under 5-ALA treatment, even in highly motile cells, indicating that Coro1A simultaneously governs invasiveness and intraoperative fluorescence detectability. Furthermore, Coro1A depletion increased sensitivity to temozolomide (TMZ) and X-ray irradiation, revealing its critical contribution to therapy resistance. Collectively, these findings establish Coro1A as a central cytoskeletal regulator that unifies invasion, diagnostic escape, and therapeutic resilience—highlighting its potential as a curative target capable of dismantling the multifaceted resistance of GBM.