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microRNAs as markers of survival and chemoresistance in pancreatic ductal adenocarcinoma

期刊

EXPERT REVIEW OF ANTICANCER THERAPY
卷 11, 期 12, 页码 1837-1842

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TAYLOR & FRANCIS LTD
DOI: 10.1586/ERA.11.184

关键词

biomarker; chemoresistance; EUS-FNA; in situ hybridization; metastamiR; metastasis; miR-10b; miR-21; pancreatic cancer; survival

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资金

  1. Worldwide Cancer Research [10-0510] Funding Source: researchfish
  2. Worldwide Cancer Research [10-0510] Funding Source: Medline

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Evaluation of: Preis M, Gardner TB, Gordon SR et al. microRNA-10b expression correlates with response to neoadjuvant therapy and survival in pancreatic ductal adenocarcinoma. Gin. Cancer Res. 17(17), 5812-5821 (2011). microRNAs (miRs) are a recently recognized class of noncoding short RNAs, 17-25 nucleotides in length, that play a role in post-transcriptional gene regulation by translational repression and/or mRNA degradation. Various miRs have been highlighted in pancreatic cancer development and metastasis, and as potential clinical diagnostic/prognostic biomarkers. Recently, studies have indicated that miRs are responsible for resistance to chemotherapeutic agents. The miR-10b has been identified as a 'metastamiR' in various tumor types, notably breast cancer, but data surrounding its relevance in pancreatic ductal adenocarcinoma has been sparse. The evaluated article presents data indicating that miR-10b is upregulated in pancreatic ductal adenocarcinoma and can be used as a diagnostic marker in endoscopic ultrasound-guided fine-needle aspiration biopsies of suspicious pancreatic lesions. In addition, miR-10b may be able to guide neoadjuvant gemcitabine-based chemoradiotherapy and predict metastatic-free survival and overall survival.

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