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βIII-微管蛋白是一种多功能蛋白,参与非小细胞肺癌的药物敏感性和肿瘤发生。

betaIII-tubulin is a multifunctional protein involved in drug sensitivity and tumorigenesis in non-small cell lung cancer.

机构信息

Children's Cancer Institute Australia, Lowy Cancer Research Centre, University of New South Wales, Randwick, New South Wales, Australia.

出版信息

Cancer Res. 2010 Jun 15;70(12):4995-5003. doi: 10.1158/0008-5472.CAN-09-4487. Epub 2010 May 25.

Abstract

Advanced non-small cell lung cancer (NSCLC) has a dismal prognosis. betaIII-Tubulin, a protein highly expressed in neuronal cells, is strongly associated with drug-refractory and aggressive NSCLC. To date, the role of this protein in in vivo drug resistance and tumorigenesis has not been determined. NSCLC cells stably expressing betaIII-tubulin short hairpin RNA displayed reduced growth and increased chemotherapy sensitivity when compared with control clones. In concordance with these results, stable suppression of betaIII-tubulin reduced the incidence and significantly delayed the growth of tumors in mice relative to controls. Our findings indicate that betaIII-tubulin mediates not only drug sensitivity but also the incidence and progression of lung cancer. betaIII-Tubulin is a cellular survival factor that, when suppressed, sensitizes cells to chemotherapy via enhanced apoptosis induction and decreased tumorigenesis. Findings establish that upregulation of a neuronal tubulin isotype is a key contributor to tumor progression and drug sensitivity in lung adenocarcinoma.

摘要

晚期非小细胞肺癌(NSCLC)预后较差。βIII-微管蛋白在神经元细胞中高度表达,与耐药性和侵袭性 NSCLC 密切相关。迄今为止,该蛋白在体内耐药性和肿瘤发生中的作用尚未确定。与对照克隆相比,稳定表达βIII-微管蛋白短发夹 RNA 的 NSCLC 细胞的生长受到抑制,化疗敏感性增加。与这些结果一致,稳定抑制βIII-微管蛋白可降低肿瘤的发生率,并显著延迟与对照相比的肿瘤生长。我们的研究结果表明,βIII-微管蛋白不仅介导药物敏感性,还介导肺癌的发生率和进展。βIII-微管蛋白是一种细胞存活因子,当被抑制时,通过增强凋亡诱导和减少肿瘤发生使细胞对化疗敏感。研究结果表明,神经元微管蛋白同工型的上调是肺腺癌肿瘤进展和药物敏感性的关键因素。

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