Long non-coding RNA orchestrates targeted-therapy resistance in renal cell carcinoma
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Department of Urology,Changzheng Hospital,Second Military Medical University,Shanghai,Department of Urology,Changzheng Hospital,Second Military Medical University,Shanghai,Department of Urology,Changzheng Hospital,Second Military Medical University,Shanghai

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Supported by National Natural Science Foundation of China (81572521) and Yangfan Talent Program of Science and Technology Commission of Shanghai Municipality (16YF1403600).

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    Abstract:

    Recently, improved comprehension of renal cell carcinoma (RCC) pathogenesis has led to the development of small molecule targeted-drug, receptor tyrosine kinase (RTK) inhibitors such as sunitinib and sorafenib, which are now the mainstay of therapeutic options for advanced RCC patients. However, 15% of advanced RCC patients are inherently refractory to targeted-drug, and most of the remaining patients end up with drug resistance and tumor progression after 6-15 months of therapy with sunitinib, resulting in the failure to efficiently prolong the survival of RCC patients. Therefore, it is urgent to explore the potential mechanisms of targeted-drug resistance and to identify the biological markers to predict efficacy of targeted-drug in RCC. Recently, we found that long non-coding RNA (lncRNA) plays a key role in target-drug resistance of RCC, which had been published in Cancer Cell, Nature Communications and Oncogene. In this comment, we systematically reviewed our research results in targeted-drug resistance of RCC. Besides, we also share our views on future directions in targeted-drug resistance, hoping to provide implications for future study.

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History
  • Received:January 13,2017
  • Revised:February 22,2017
  • Adopted:February 28,2017
  • Online: March 31,2017
  • Published:
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