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剪接变异体作为结直肠癌的生物标志物。

Alternative spliced variants as biomarkers of colorectal cancer.

机构信息

College of Bioengineering, Chongqing University, Chongqing 400044, China.

出版信息

Curr Drug Metab. 2011 Dec;12(10):966-74. doi: 10.2174/138920011798062355.

Abstract

Surgical resection and adjuvant therapy, which mainly involves 5-fluorouracil (5-FU), irinotecan (CPT-11), oxaliplatin (LOHP) chemotherapy and recently targeted therapy, are the most common treatments of colorectal cancer (CRC). As to improve the therapeutic efficacy and assist with therapeutic decisions, there is an urgent need for prognostic and predictive molecular biomarkers. Recent evidence demonstrates that aberrations in alternative splicing process of cancer will provide candidate biomarkers for cancers to meet this need. In this review, we outline the fundamental mechanism of alternative splicing that plays a major role in protein diversity, and summarize the relationship between imbalance alternative splicing with cancer. Moreover, several alternative spliced variants and cancer-specific splicing events at the mRNA level in CRC, which may serve as diagnostic, predictive, prognostic markers of CRC, are also discussed. These specific splice variants or the RNA splicing machinery will be new, potential targets for the treatment of CRC that offers a specific site of anti-cancer chemotherapy.

摘要

手术切除和辅助治疗(主要涉及氟尿嘧啶(5-FU)、伊立替康(CPT-11)、奥沙利铂(LOHP)化疗以及最近的靶向治疗)是结直肠癌(CRC)最常见的治疗方法。为了提高治疗效果并辅助治疗决策,迫切需要预后和预测性的分子生物标志物。最近的证据表明,癌症中选择性剪接过程的异常为癌症提供了候选生物标志物来满足这一需求。在这篇综述中,我们概述了选择性剪接的基本机制,该机制在蛋白质多样性中起主要作用,并总结了不平衡选择性剪接与癌症之间的关系。此外,还讨论了 CRC 中 mRNA 水平上的几种选择性剪接变体和癌症特异性剪接事件,这些变体或事件可能作为 CRC 的诊断、预测、预后标志物。这些特定的剪接变体或 RNA 剪接机制将为 CRC 的治疗提供新的、潜在的靶点,为癌症化疗提供特定的作用位点。

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